Research Scientist Salary in San Diego, CA

Company DescriptionThe work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.If you're looking for a rewarding career, a place to call home, apply with us today!.Job DescriptionThis is a technical position within a Cell & Gene Therapy group in La Jolla, CA to RNA purification and characterization in support of novel discovery programs. The candidate will be able to contribute to new technology development and concept generation. The ideal candidate will have a background in chemical engineering, RNA purification or other biomolecules (especially viral vectors) and some experience in an industry setting (especially CRO work).Core Responsibilities:• Support RNA manufacturing process development by assisting in RNA purification and chromatographic studies.• Aid and support system programming, preparation, maintenance and troubleshooting AKTA chromatography systems.• Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to meet project deadlines.• Collect and evaluate data; prepare reports, summaries, and presentations; maintain and update laboratory notebook and the laboratory information management system.• Capability to multi-task, be independent, self-motivated, as well as work in a highly collaborative setting.QualificationsBachelor's degree in a science related discipline with 2-4 years as a scientist in a research, laboratory setting, or biotech/pharma company (CRO experience ideal).General understanding of virology, cell biology vectors, RNA purification/characterization.Experience with AKTA chromatography and Unicorn software.Excellent organization skillsExcellent written and verbal communicationAuthorization to work in the United States indefinitely without restriction or sponsorship.Additional InformationSalary of $26.12 - $29.10/hour.Position is full-time, Monday to Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of La Jolla, CA are encouraged to apply.What we Offer:Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company DescriptionThe work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.If you're looking for a rewarding career, a place to call home, apply with us today!.Job DescriptionThis is a technical position within a Cell & Gene Therapy group in La Jolla, CA to RNA purification and characterization in support of novel discovery programs. The candidate will be able to contribute to new technology development and concept generation. The ideal candidate will have a background in chemical engineering, RNA purification or other biomolecules (especially viral vectors) and some experience in an industry setting (especially CRO work).Core Responsibilities:• Support RNA manufacturing process development by assisting in RNA purification and chromatographic studies.• Aid and support system programming, preparation, maintenance and troubleshooting AKTA chromatography systems.• Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to meet project deadlines.• Collect and evaluate data; prepare reports, summaries, and presentations; maintain and update laboratory notebook and the laboratory information management system.• Capability to multi-task, be independent, self-motivated, as well as work in a highly collaborative setting.QualificationsBachelor's degree in a science related discipline with 2-4 years as a scientist in a research, laboratory setting, or biotech/pharma company (CRO experience ideal).General understanding of virology, cell biology vectors, RNA purification/characterization.Experience with AKTA chromatography and Unicorn software.Excellent organization skillsExcellent written and verbal communicationAuthorization to work in the United States indefinitely without restriction or sponsorship.Additional InformationSalary of $26.12 - $29.10/hour.Position is full-time, Monday to Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of La Jolla, CA are encouraged to apply.What we Offer:Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Job Description SummaryJOB SUMMARYWe are seeking a highly motivated and organized Scientist III to contribute to the research and development of monoclonal antibodies in our Antibody Technologes team. This individual will be responsible for working in a dynamic team environment and will contribute to multiple workstreams including but not limited to antibody screening using flow cytometry, hybridoma tissue culture and development, and recombinant protein expression. The position requires extensive hands-on experience with flow cytometry, expertise in tissue culture, and an understanding of biochemistry and molecular biology. The successful candidate is expected to design and execute experiments, be detail-oriented, analyze and interpret data, contribute to troubleshooting efforts, identify and implement process improvements and will be accountable for preparing and presenting data at lab meetings regarding required tasks and expected results.Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. DUTIES AND RESPONSIBILITIESResponsible for the design and execution of experiments with varying complexity using multi-color Flow Cytometry.Analyze data using FCS Express and FlowJo software, report test results including completion of all required documentation and database entries as required by protocols and SOPs.Responsible for transfection and expression of antibodies in cell lines, hybridoma tissue culture, and culture of various cell lines for testing. Specific requirement for hands-on experience with aseptic technique and cell-culture techniques.Responsible for executing experiments using liquid handling robots and automation machineryDay-to-day problem solving and cross-functional team-based activities to ensure that daily operations and timelines are met.Contribute to identification and implementation of process improvement projectsTrain junior scientists on laboratory techniques and business processesIndependently analyze own research data, solve problems with minimal guidance and effectively plan follow up experiments. Will be expected to efficiently prioritize individual workload.Involvement with scheduling, operational and maintenance duties required within the laboratory.KNOWLEDGE AND SKILLSHands on experience designing, performing, and analyzing flow cytometry experiments, preferably on BD flow cytometers (LSRII, LSR Fortessa, Canto, Aria).Proficient in tissue culture techniques; including transfection of cells for protein expression.Software: BD FACS Diva, FlowJo, FCS Express, and Microsoft Office Suite.Familiarity with molecular biology (DNA preparation)Familiarity with assay automation.Effective interpersonal skills and ability to work in a cross-functional team-oriented environment to achieve organizational goals.Effective written and oral communication skills.Demonstrated ability to follow established policies and procedures.Demonstrated ability to keep neat, accurate, and complete records.Effective analytical and problem-solving skills.EDUCATION AND EXPERIENCEA Bachelor's or Master of Science degree in cellular or molecular biology, immunology, cell biology or related scientific discipline and a minimum of 2-5 years of laboratory experience required. Flow cytometry and tissue culture experience required.For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.Why Join Us?A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit https://bd.com/careers Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. #earlycareerPrimary Work LocationUSA CA - San Diego (BDB)Additional LocationsWork ShiftNA (United States of America)At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You .Salary ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary offered to a successful candidate is based on experience, education, skills, and actual work location. Salary ranges may vary for Field-based and Remote roles. Salary Range Information $79,000.00 - $130,400.00 USD Annual

Innova Solutions is immediately hiring for a Research ScientistTittle - Research Scientist Duration - 12 Months Location-San Diego, CA. 100% Onsite. Pay Range*: $54 - $55 per hour. As a Research Scientist you will: Job Description: Utilize and develop multiple disease models to design target validation studies and relevant assays in support of SAR, mechanism of action, mechanisms of resistance, biomarker selection, and disease positioning. Develop and implement cell-based assays to address both tumor intrinsic cellular biology and immune-based mechanisms of action for potential drug candidates Design and conduct essential mechanistic experiments in cell biology, cellular biochemistry, molecular biology, and assay development The ideal candidate will have: Ph.D. in cell biology, immunology, molecular biology, or equivalent field with 0-2 years of post-doc or industry experience, or M.S. degree with 3+ years of experience, or Bachelor's degree with 5+ years of experience in the biopharmaceutical industry developing and optimizing cell-based assays, preferably in Oncology Strong background and experience in cancer research with training in molecular and cell biology Extensive experience using multi-parameter flow cytometry in the context of primary immune cell isolation and characterization is required. Extensive hands-on experience with mammalian cell culture, molecular and cellular technologies (e.g., CRISPR/Cas9 knock-in/out, lentiviral transduction, western blotting, quantitative PCR,) and functional assays (e.g., proliferation, apoptosis, cell cycle) is essential Experience in utilizing platforms including IncuCyte, JESS, Flow based cell sorter, ELISA, and MSD in the context of oncology-based drug discovery is a plus. Proficiency in scientific data analysis programs including GraphPad Prism, FlowJo, Microsoft Excel/Powerpoint, is required Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. ASK ME HOW. Thank you! Aritra Roy 4702230481 [email protected] PAY RANGE AND BENEFITS: Pay Range*: $54 - $55 per hour. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: One of Largest IT Consulting Staffing firms in the USA - Recognized as #4 by Staffing Industry Analysts (SIA 2022) ClearlyRated® Client Diamond Award Winner (2020) One of the Largest Certified MBE Companies in the NMSDC Network (2022) Advanced Tier Services partner with AWS and Gold with MS Website: https://www.innovasolutions.com/ Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at [email protected] or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws

Our Biotech client is looking to add a Contract Scientist to their growing Bioanalytical team. This is an onsite, lab-based position in San Diego, California.Responsibilities:Assay development and designing in vitro and in vivo studiesMethod development of pharmacokinetic and immunogenicity assaysWork collaboratively with existing team and partnered CRORequired Qualifications: BS Degree requiredPrevious experience in biotech/pharmaqPCR, MSD, siRNA experienceAbility to troubleshoot and solve problemsSolid written and oral communication skillsStrong interpersonal skills, and attention to detail are necessaryIf you meet the required qualifications and are interested in this role, please apply today.Clinical Resource Network Distinction CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.About CRNFounded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn.Opportunity Awaits.

Job Description - Primary Cell & Product Department:The Scientist/Senior Scientist in Primary/Product Department plays a role in the fast-paced and dynamic manufacture as well as NPSI (New Products & Service Innovation) process. She/he will participate in the Service projects and Product generation, and the major responsibilities include but not limited to the primary cell isolation, and performing the various assays using primary cells.Major Roles and ResponsibilitiesParticipate in/Lead Primary Cell Isolation related Service Projects & Primary products generation from human and animal tissue specimens, especially the cells from human large organs, such as the ones in the gastrointestinal system, Liver or kidney.Participate in/Lead the Primary Cell Product Inventory maintenance by following iXCells manufacturing protocol, within the budget control and timeline.Optimize the existing product generation protocol, to maximize the productivity and minimize the unit cost. Participate in/Lead NPSI projects for the new primary cell product manufacturing, and provide the detailed Q&C criteria for the technical transfer.Assist in training of sales and technical support teams.Mentor, train and/or coach Research Associates.Be prepared to support the other teams when needed.Represent the company at professional meetings both within and outside of the companyQualificationsMS with 5+ or Ph.D. with 2+ years working experience in biology, pharmacology or closely related fields. Candidates with industrial experience are preferred.Candidates with Primary Cell Isolation experience are preferred. The experience with cell isolation from human large organs or tissues is plus.Proficiency in rodent dissection, primary cell culture, immunofluorescence staining, flow cytometry, etc.Ability to multitask across several research areas/projectsAbility to work in a fast-paced environment and adapt to changes quicklyDetail-oriented, with excellent organization and record-keeping skillsStrong computer skills with demonstrated proficiency in MS Office and other software for sequencing analysis and data graphingAble to work in a team-oriented environment. Effectively collaborate across functional teamsJob Type: Full-timeBe aware that your job responsibilities may change at any time during your employment. From time to time, you may be asked to work on special projects, or to assist with other work necessary or important to the operation of your department or iXCells. Your cooperation and assistance in performing such additional work is expected. iXCells reserves the right, at any time, with or without notice, to alter or change job responsibilities, reassign or transfer job positions, or assign additional job responsibilities.

Job Title: Scientist/Sr. ScientistLocation: San DiegoBackgroundRayzeBio is a dynamic biotechnology company headquartered in San Diego, CA. Launched in late 2020 and recently acquired by Bristol Myers Squibb (BMS) as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio will operate as a standalone entity within the BMS organization, maintaining its biotech culture with the opportunity to leverage the best-in-class oncology capabilities of BMS. RayzeBio is developing innovative drugs against targets of solid tumors. The lead asset, RYZ101, is in Phase 3 testing for patients with gastroenteropancreatic neuroendocrine tumors (GEP-NETs), as well as earlier stage testing for patients with small cell lung cancer (SCLC) and breast cancer. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.Job DescriptionThe Scientist/Sr. Scientist will design and synthesize novel chemical constructs as potential new RPT therapies for cancer treatments. The Scientist/Sr. Scientist will be a highly motivated and technically skilled synthetic organic, peptide or medicinal chemist with excellent interpersonal and communication skills. The role will offer an opportunity to work as functional lead on multiple projects ranging from target selection through candidate nomination stages and can be expected to lead early-stage projects in an interdisciplinary setting. The role is highly technical and will need a person who enjoys leading from the bench with high productivity and data analysis skills and a comfort level in working under tight timelines. The role requires an ability and willingness to work with radioactive isotopes.Job ResponsibilitiesEssential duties and responsibilities include the following. Other duties may be assigned.• Design and synthesize novel peptide/small molecule compounds in support of SAR campaigns for pipeline projects.• Contribute towards developing SAR on assigned projects, design and synthesize key target molecules to assess chemical/biological hypothesis.• Independently plan and execute organic synthesis routes for complex molecules. Utilize modern purification and analytical tools to support synthesis and characterization of target compounds.• Work in close collaboration with interdisciplinary team members to provide needed chemistry support to guide programs through lead identification/optimization phases.• Work closely with chemists, DMPK, imaging and in vitro/vivo teams to ensure that target compounds are generated in a timely manner to support the screening funnel.• Contribute experimental efforts in support of target selection and initiation of new TRP projects.• Keep abreast of the literature in the field of RPTs, identify novel concepts and ideas to help advance the state of art in RPT field.• Contribute towards IP filings and drafting of publications, presentations.• Routinely present research findings, project updates in interdisciplinary team settings.• Adhere rigorously to safety guidelines, regulatory standards and company policies and ensure a safe working environment.• Identify external partners, KOLs, outside expertise that will help advance the pipeline.• Supervise the work of junior scientists and ensure experimental rigor and high quality.Education and Experience• PhD in synthetic organic, peptide or medicinal chemistry with 2+ years of post-PhD/postdoc experience or BS with 15+ years experience in Pharmaceutical/biotech R&D environments demonstrating successful accomplishments and productivity.• Experience in working on targeted cancer therapy modalities such as RPTs, ADCs, PDCs is highly desirable.Skills and Qualifications• Well versed in modern synthetic organic/peptide/med chem principles and demonstrated track record of high productivity and achievements in the lab.• High scientific curiosity and a learning mindset coupled with strong technical problem-solving skills and strong understanding of the concepts of drug design, SAR analysis, ADME/PK is important.• The ability to share data and collaborate with cross functional team members is critical as is the ability to effectively interpret data and plan experiments without supervision.• Excellent written and oral communication and presentation skills and ability to work in a fast-paced, dynamic, and collaborative environment.• Demonstrated ability to supervise and effectively guide the work of junior scientists and demonstrated ability of productivity in an industrial drug discovery setting.• Ability to work with radioisotopes with strict adherence to radiation safety protocols.The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed.Final, individual compensation will be decided based on demonstrated experience.Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Employee assistance programs (EAP) and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance and supplemental health insurance. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, and sick time off. Parental, caregiver, bereavement, and military leave. Other perks like tuition reimbursement.

Position OverviewThe Senior Scientist is responsible for studies to support the development of applications and products built on the company's technology platforms. The Senior Scientist is a key role on the team, performing preparative and analytical protein chemistry work using antibodies and other proteins. This hands-on position provides the opportunity to contribute to development of an innovative diagnostic platform as part of our new company. The individual in this role will efficiently design and execute experiments, perform appropriate statistical data analyses, and regularly communicate results and observations effectively in presentations to inter-disciplinary teams. The individual must be a detail-oriented, innovative teammate with a solid understanding of immunochemistry and protein biochemistry, and have prior hands-on experience working with antibodies and common biochemical techniques. The Senior Scientist must have excellent cross-functional communication skills, a goal-oriented mentality, and a strong sense of ownership and drive to meet project goals and timelines.Key ResponsibilitiesFollowing are the major results needed for the role.Additional responsibilities, tasks and duties will be assigned and required as needed.Plan, perform, and optimize antibody conjugations, fragmentations, and purificationsIndependently design, create, and troubleshoot recombinant protein-bead constructsDevelop insights into interaction of company technology with biological variables, leading to enhanced detection and quantification of biomarkers.Find creative and practical solutions to a wide range of cross-disciplinary technical challenges.Use analytical and statistical techniques to characterize experimental results.Effectively troubleshoot workflows and experiments on a proactive basis, taking ownership of results, interpretations, scope, strategy, and tactics on a project level.Maintain a clear and complete log of research results in electronic form, following quality systems requirements; organize experiments and findings into databases.Effectively communicate experimental findings in written and verbal formats during internal meetings.Partner effectively with other members of the Assay Development team as well as all other departments in support of company objectives.Ensure laboratory activities are performed in compliance with safety guidelines and best practices.Serve as mentor for other scientists/engineers and research associates in areas of expertise; may be responsible for direct reports.Builds consensus and gains support of key stakeholders. Coordinates across and within the organization to determine the appropriate resources and parameters to complete projects in the most efficient manner. Is a driver of change and decision-making within the department; contributions are essential to the department and company's objectives. Ensures a high degree of quality in the department's work.Demonstrates group-wide influence and scientific/technical competence, in addition to having a strong business-sense as it relates to the needs and requirements.Exercises independent judgment in creating and innovating methods, techniques and evaluation criteria for obtaining results. Demonstrates ability to discover and identify processes, novel science and technology, which leads to increased productivity and results.May provide task/project leadership, guidance and mentoring of others while being equitable and respectful to everyone. Responsible for compliance with all company policies outlined in the Employee Handbook.Responsible for compliance with quality procedures and all regulatory requirements.Consistently exhibits respect and build trust through openness, collaboration, and support of one another.Operates with respect, humbleness, integrity, honesty, and transparency.Demonstrates inclusivity, ongoing communication, and a positive outlook with both internal and external team members and customers.May be required to travel up to 5% of the time.Will be exposed to company confidential information which must not be divulged.Experience, Education, and Skills Required:Below are the minimum skills, formal education, certifications or training, and practical experience required to perform the general functions and duties of the role.Typically requires a PhD in a scientific discipline with at least 5 years of post-PhD experience; or equivalent combination of education and experience.Solid experience in and knowledge of antibody fundamentals and pairing, including antibody fragmentation, conjugation, and purification is required.Working knowledge of buffers and protein solubilitySolid working experience in a wide variety of protein purification, detection, and identification techniques (e.g.ELISAs, Western Blots, chromatography, immunoprecipitation, immunocytochemistry, enzyme assays).Understanding of protein interactions, antigen-antibody interaction kineticsExperience in IVD assay development is a plus.Expertise in the design and development of biochemical and immunoassays is required.Understanding of experimental design - selection of appropriate controls, variables, and conditions is requiredSelf-motivated with superior organization and observation skills.Innovative in developing new assays or approaches to meet desired goalsAbility to identify and resolve technical challengesExpertise in the application of statistical analysis and software (e.g., GraphPad Prism) to drive decision making.Ability to communicate research results in a clear and concise fashion.Ability to work in a team-based setting.Desire and drive to work in a fast-paced, hands-on environment.Demonstrates advanced scientific/technical expertise and implementing innovative solutions. Regularly collaborates with others and provides independent thought and strategy for large scope solutions. Proactively contributes to and possesses a high level of understanding of product requirements, industry needs, and patent applications. Anticipates potential complex problems in which analysis of situations or data requires an in-depth evaluation. Has a reputation as an emerging technical expert and mentor with sustained performance and accomplishments. Demonstrates an understanding of Six-Sigma principles and good laboratory practices.Must be able to understand job duties and responsibilities, have the necessary skills/knowledge, and be willing and able to continue learning and growing within the field.Must be comfortable in an early-stage company where tasks, responsibilities or duties assigned may be outside of position scope.Must be nimble and comfortable with rapidly changing priorities and responsibilities.Must be skilled at managing a significant workload and obtaining successful results, taking on additional responsibility and managing priorities as needed.Must be proactive and effective in achieving solutions and using data to achieve results.Strong verbal and written communication skills with the ability to produce accurate, punctual reports/information, as required, and thoroughly share information with others. Must be able to read, write and speak effectively.Exceptional listening skills with the ability to seek constructive feedback, build relationships, promote teamwork, and remain flexible, humble, and open-minded.Capable of following realistic plans, goal setting, resource management, contingency planning, coordinating, and cooperating with others.Capable of working thoughtfully under pressure and in a timely manner.Must be comfortable and capable of performing the job within the physical requirements and conditions necessary for the role.

*****Only screening candidates with recent clinical science experience*****RESPONSIBLITIES:• Contribute to the design, implementation (study start-up, execution, analysis), review, and communication of clinical protocols and study reports for scientific and operational accuracy• Responsible for analyzing data and timely delivery of high-quality clinical study data analysis for publications and scientific presentations; present clinical study results to the cross functional team and external stakeholders• Work with the Medical Director to review clinical data and develop clinical development strategy with KOLs• Collaborate with the Medical Director and Clinical Operations to expedite execution of clinical trials• Interpret and communicate clinical information including literature reviews, competitive intelligence, and changing treatment paradigms to apply knowledge and support a robust clinical development strategy• Identify, qualify, manage, and maintain relations with clinical trial sites, including collaborating with Principal Investigators, CRO and field team to develop robust study protocols, drive site selection, and patient recruitment programs that deliver enrollmentREQUIREMENTS:• Masters/PhD degree in health science field, PharmD, MD (non-US MD acceptable), MSN, or other relevant advanced degree in a health science field.• 5 years of clinical research experience in oncology clinical trials, including a minimum of 8-10 years industry experience. Experience with kinase inhibitors and/or pediatric drug development experience highly desirable.• Excellent time management skills • Excellent working knowledge of ICH GCP guidelines, CFR, EMA, and HIPAA regulations• Able to work independently and make appropriate strategic decisions to operationalize and move clinical trials forward, in collaboration with the Medical Monitor• Excellent written and oral communication skills • Excellent presentation skills• The ability to manage multiple priorities• Experience operating effectively within a matrixed work from home environment, specifically in a healthcare biotech/pharmaceutical start-up setting• Excellent computer skills (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook, and IXRS/EDC platforms)

The duties and responsibilities contained in the job description are intended to be examples of the accountabilities for which the person in the position will demonstrate competency through performance. The job description is not intended to be an all-inclusive list. Duties and responsibilities are subject to change and other duties may be assigned as necessary within the scope of the Research Administrative Services (RAS) department.Summary: The Research Administrative Coordinator III (RAC III) reports directly to the RAS Director and provides advanced level administrative support to multiple Institute Faculty (Principal Investigators) and affiliated lab personnel, including pre/post-award coordination, addressing lab related inquiries, maintaining filing systems, processing paperwork, composing correspondence, coordinating meetings, and making travel arrangements. Receives direction from RAS department Supervisor, RAS Director, and PI, and completes all duties in accordance with Institute and department policies and procedures and in collaboration with other Administrative or Scientific departments. Works both independently and as a team member; with limited guidance, prioritizes and executes responsibilities.The Research Administrative Coordinator role is a career progression series with increasing levels of competence and responsibility. The position provides administrative support to the Institute's faculty and their labs through direct service or cross trained personnel. Duties and Responsibilities:• Supports faculty and lab administrative activities through demonstrated competency in all responsibilities of the Research Administrative Coordinator series including but not limited to general office duties, paper and electronic file maintenance, and preparation of correspondence.• Serves as the lab staff's first point of contact for assistance with other administrative departments.• Establishes priorities and organizes workload to meet deadlines. Utilizes calendaring resources to ensure Faculty receives adequate information and reminders on approaching deadlines to ensure goals and objectives are met.• Provides administrative and quality control regarding purchasing card statements and expense reports, in compliance with all Institute policies and deadlines; in addition to other finance related duties (i.e., preparation of check requests, compiling documentation for reimbursements, etc.).• Maintains monthly summary of financial reports, time and effort certificates, and ensures timely submission of approved financial reports with Research Accounting.• Oversees and participates in the distribution of communications and information to the lab group members.• Implements and maintains data tracking and evaluation of awarded grants, independently or collaboratively, assists in the compilation of progress report(s) and final progress report(s) with Sponsored Research Office (SRO), Research Accounting, and Intellectual Property (Invention and Patent) by preparing material for the reports through computerized data, library materials, external agencies, etc.• Serves as liaison with administrative departments including, but not limited to: Payroll, IT, Research Accounting, Finance, Facilities, Procurement, Human Resources, and Sponsored Research, and the Office of Education, Training, and International Services (OETIS). • Coordinates with HR and OETIS regarding lab recruitments per institute policy and procedures; tracks information regarding recruitment efforts, lab promotion activity, and regularly communicates this information with assigned faculty.• Coordinates all travel arrangements; flights, lodging, ground transportation, meals, appropriate documentation (W9, media release, etc.) forms for invited speakers, recruitment candidates, and for the PI when the need arises.• Coordinates, schedules, and facilitates complex activities and a variety of meetings, conferences, seminars/symposia with internal and external collaborators; extensive event project planning (venue selection, hotel contracts, travel, etc.) independently or in collaboration with the RAS Events Team.• Maintains calendar for assigned faculty as needed or requested.• Tracks, maintains, and collects supporting documentation of faculty activity to ensure appropriate information is provided to Finance department following Institute, NIH, NCI, and other funding agency compliance guidelines.• Maintains familiarity with federal and state grant rules and processes.• Works with faculty to prepare and maintain biographies, statements of research, bibliographies, lists of publications, new publications and curriculum vitae. Manages submissions of publications to the digital archive PubMed Central.• Assists and maintains manuscript submission(s) and compliance with NIH Public Access Policy; organizes and formats manuscripts in accordance with journal guidelines, proofreads draft(s), manipulates/positions/organizes graphs, figures, tables, and charts, and uses EndNote bibliography software in providing citations for the manuscript.• Renews PI's annual membership in scientific societies.• Perform other related tasks, duties and responsibilities as required, assigned or directed.Required Education, Experience and Skills:• Bachelor's Degree in a related field (Business Management, Public Administration, Communications) and 2 years' experience; Technical training and experience from which comparable knowledge, skills and abilities have been attained may be substitute for education (4-6 years of directly related work experience).• Experience (4-6 years) providing administrative support in a high-demand, challenging environment in academia or scientific research (preferred); previous grant administration; pre- and post-award.• Excellent attention to detail, organizational and time management skills, demonstrating an ability to set up workflow processes and prioritize responsibilities.• Able to work onsite regularly to facilitate completion of training, meet faculty and lab needs, and/or the Institute's needs.• Able to consistently arrive at work on time and be present when needed; ensures work responsibilities are covered when planned absences arise.• Proficiency with office equipment, computers, and Microsoft Office suite.• Intermediate-advance skill in virtual meeting setup and hosting in Zoom and Microsoft Office Teams.• Working knowledge and experience of federal, state, and local agency practices, processes, and guidelines, with a view to familiarity with other sponsors.• Proven experience in all aspects of coordinating meetings, conferences, special events, including site selection, catering, audiovisual services, travel arrangements (domestic & international), procurement, honoraria, travel reimbursements.Additional Requirements and Preferred Qualifications:• Able to meet the Institute's Performance Standards; learn and be proficient with pertinent internal systems.• Able to demonstrate respect and civility in all aspects of the job; maintain confidentiality and exercise discretion and/or judgment.• Able to work under pressure, prioritize on short notice, meet, or exceed strict deadlines, and support multiple projects with varying degrees of complexity. Able to be flexible and adaptable to frequent change and unexpected delays.• Able to work independently as well as in a team environment while providing administrative support in an academic, scientific, research environment. Compensation:The expected compensation for this position is between $65,000 - $80,000/annually commensurate with experience.Sanford Burnham Prebys celebrates the rich diversity of our scientists, students and staff, who hail from more than 30 countries. Our diverse and inclusive environment catalyzes innovation and fuels discovery, enhancing the value and impact of our research.We welcome talented individuals of all backgrounds regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, military or veteran status. We are proud to be an equal opportunity employer.If you need an accommodation seeking employment with Sanford Burnham Prebys, please email [email protected]. Accommodations are made on a case-by-case basis.Sanford Burnham PrebysPI249872895