Dermatology Salary in New Jersey, USA

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CRL has been an independent, third-party testing laboratory for the Cosmetics and Personal Care Industry for over twenty-five years. Our facility located in Piscataway, is home to our technical staff and medical professionals from the practice of Dermatology. We are currently seeking a Board-Certified Ophthalmologist to add to our professional consulting staff.We find that our medical professionals enjoy the flexibility that a clinical testing schedule can provide in being able to work your practice hours around our lab visit hours. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.We are anxious to expand our team of clinical professionals to continue to provide excellent clinical testing services to our clients.Hourly compensation rates can be discussed on an individual basis.QualificationsBelow is a brief example of the types of responsibilities required of you in this role:Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. This also involves signing the protocol and final report for these studies.At homereview and approval of clinical study protocols and reports either as PI or Sub I.Performing ophthalmologyexams for Clinical Studies anywhere from a few hours to a few days per month as listed above including but not limited to the following parameters:The degree of lacrimation.Redness, scaling, swelling, and Meibomian gland secretions of the eyelids.Evidence of inflammation or follicular and/or papillary reaction of the palpebral conjunctivae.Evidence of inflammation or any other abnormalities of the bulbar conjunctivae.Evidence of inflammation, neovascularization, edema, infiltrates, opacities and/or epithelial defects of the cornea.Evidence of scratches and deposits on hard or rigid gas permeable contact lenses.Evidence of deposits, as well as changes in contact lens color, on soft contact lenses.Additional InformationTo learn more about Eurofins, please explore our website www.eurofinsus.com.Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CRL has been an independent, third-party testing laboratory for the Cosmetics and Personal Care Industry for over twenty-five years. Our facility located in Piscataway, is home to our technical staff and medical professionals from the practice of Dermatology. We are currently seeking a Board-Certified Gynecologist to add to our professional consulting staff.We find that our medical professionals enjoy the flexibility that a clinical testing schedule can provide in being able to work your practice hours around our lab visit hours. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.We are anxious to expand our team of clinical professionals to continue to provide excellent clinical testing services to our clients.Hourly compensation rates can be discussed on an individual basis.QualificationsBelow is a brief example of the types of responsibilities required of you in this role:Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. This also involves signing the protocol and final report for these studies.At homereview and approval of clinical study protocols and reports either as PI or Sub I.Performing Gynecologicalexams for Clinical Studies anywhere from a few hours to a few days per month as listed above including but not limited to the following parameters:ErythemaEdemaDrynessAdditional InformationTo learn more about Eurofins, please explore our website www.eurofinsus.com.Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CRL has been an independent, third-party testing laboratory for the Cosmetics and Personal Care Industry for over twenty-five years. Our facility located in Piscataway, is home to our technical staff and medical professionals from the practice of Dermatology. We are currently seeking a Board-Certified Dermatologist to add to our professional consulting staff.We find that our medical professionals enjoy the flexibility that a clinical testing schedule can provide in being able to work your practice hours around our lab visit hours. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.We are anxious to expand our team of clinical professionals to continue to provide excellent clinical testing services to our clients.Hourly compensation rates can be discussed on an individual basis.QualificationsBelow is a brief example of the types of responsibilities required of you in this role:Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. This also involves signing the protocol and final report for these studies.At homereview and approval of clinical study protocols and reports either as PI or Sub I.Performing oral exams for Clinical Studies anywhere from a few hours to a few days per month as listed above including but not limited to the following parameters:ErythemaEdemaDrynessAdditional InformationTo learn more about Eurofins, please explore our website www.eurofinsus.com.Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CRL has been an independent, third-party testing laboratory for the Cosmetics and Personal Care Industry for over twenty-five years. Our facility located in Piscataway, NJ, is home to our technical staff and medical professionals from the practice of Dermatology. We are currently seeking a Board-Certified Dentist to add to our professional consulting staff.We find that our medical professionals enjoy the flexibility that a clinical testing schedule can provide in being able to work your practice hours around our lab visit hours. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.We are anxious to expand our team of clinical professionals to continue to provide excellent clinical testing services to our clients.Hourly compensation rates can be discussed on an individual basis.QualificationsBelow is a brief example of the types of responsibilities required of you in this role:Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. This also involves signing the protocol and final report for these studies.At homereview and approval of clinical study protocols and reports either as PI or Sub I.Performing oral exams for Clinical Studies anywhere from a few hours to a few days per month as listed above including but not limited to the following parameters:ErythemaEdemaDrynessUlcerationSloughingAdditional InformationTo learn more about Eurofins, please explore our website www.eurofinsus.com.Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Physician Dermatology $230K - $260KLocation: Freehold, NJMust Have Strong Dermatology KnowledgeAmazing Doctors and Staff!Full Time PositionMonday - Friday 8 am - 5 pmNo Nights or No Weekends!Benefit PackageNew Residency Dermatology Grads Are WelcomePlease Apply By CV or Resume

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CRL has been an independent, third-party testing laboratory for the Cosmetics and Personal Care Industry for over twenty-five years. Our facility located in Piscataway, NJ, is home to our technical staff and medical professionals from the practice of Dermatology. We are currently seeking a Board-Certified Podiatrist to add to our professional consulting staff.We find that our medical professionals enjoy the flexibility that a clinical testing schedule can provide in being able to work your practice hours around our lab visit hours. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.We are anxious to expand our team of clinical professionals to continue to provide excellent clinical testing services to our clients.Hourly compensation rates can be discussed on an individual basis.We are looking for availability during May and June of this year. The schedule will be discussed prior to the study and will be determined by your availability.QualificationsBelow is a brief example of the types of responsibilities required of you in this role:Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. This also involves signing the protocol and final report for these studies.At homereview and approval of clinical study protocols and reports either as PI or Sub I.This role will be involved in aclinical study testing the efficacy of insoles for the following: Plantar Fasciitis, High Arch, Flat Feet, Heel Spur, Other back, knee and foot conditions.Additional InformationTo learn more about Eurofins, please explore our website www.eurofinsus.com.For further inquiry regarding this position please [email protected] is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company DescriptionEurofins 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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionEurofins CRL has been an independent, third-party testing laboratory for the Cosmetics and Personal Care Industry for over twenty-five years. Our facility located in Piscataway, NJ, is home to our technical staff and medical professionals from the practice of Dermatology. We are currently seeking a Board-Certified Pediatrician to add to our professional consulting staff.We find that our medical professionals enjoy the flexibility that a clinical testing schedule can provide in being able to work your practice hours around our lab visit hours. It is an excellent opportunity to increase your experience in the clinical testing arena and potentially lead to industry partnerships and or publications.We are anxious to expand our team of clinical professionals to continue to provide excellent clinical testing services to our clients.Hourly compensation rates can be discussed on an individual basis.QualificationsBelow is a brief example of the types of responsibilities required of you in this role:Listing as PI (Principal Investigator) or Sub I (Sub-Investigator) on Clinical Studies for Cosmetics, Personal care and possibly OTC products. This also involves signing the protocol and final report for these studies.At homereview and approval of clinical study protocols and reports either as PI or Sub I.Performing Pediatric exams for Clinical Studies anywhere from a few hours to a few days per month as listed above including but not limited to the following parameters:ErythemaEdemaDrynessAdditional InformationTo learn more about Eurofins, please explore our website www.eurofinsus.com.For further inquiry regarding this position please [email protected] is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Nurse Practitioner Dermatology $140K - $160KORPhysician Assistant Dermatology $140K - $160KLocation: Freehold, NJMust Have 3 Years Plus Of Strong Dermatology Experience On TheJob Hands On!Amazing Doctor and Staff!Full Time PositionMonday - Friday 8 am - 5 pmNo Nights or No Weekends!Benefit PackageSorry No New Grads!Please Apply By CV or Resume

The Dermatology Marketing Communications (MarCom) Manager plays a key role in enabling the success of marketing efforts in a dynamic, diverse, and growing business unit. The MarCom Manager leads the Content Review and Clearance (CRC) process of communication materials, ensuring consistent and timely messaging across brands, therapeutic areas, programs, and customer segments. The MarCom Manager also is responsible for execution excellence, and ensuring that all communications tactics are delivered on strategy, on time, and within budget.In this role, the MarCom Manager will partner with our Dermatology Therapeutic Area Team, across a variety of brands within the portfolio and different teams including Legal, Regulatory Affairs, Medical Affairs, and Communications.Key ResponsibilitiesA proven ability to think strategically.Broad understanding of the full suite of integrated communications disciplines and solutions.An innate curiosity, and "always-on" desire to find a better way of doing things.Proficiency at problem-solving and coming to the table with a workable solution for every problem.Strength in team and relationship-building.Desire and ability to work within a strong team-oriented environment.An ability to develop and implement plans and programs with strong follow-up and accountability in achieving results.An ability to effectively manage communications agencies, fueled by a keen understanding of how agencies work.Impeccable communication skills, both written and verbal.Demonstrated ability to provide innovative solutions to meet marketing objectives and business strategies.Proven record of initiative, resourcefulness, and willingness to accept challenges.Proven experience in project management and meeting deadlines.Demonstrated strong level of negotiation and influence skills, including the ability to motivate and forge consensus among peers.Ability to juggle multiple responsibilities, work under tight and frequent deadlines, and be nimble in a fast-paced, results-oriented environment.Help manage the planning, development, and implementation of communications plans and programs that help accomplish business and marketing objectives.Ensure all communications touchpoints align with segment and brand strategies and that all messaging is appropriate and consistent across mediums and portfolios.Provide strategic counsel to Portfolio Growth Strategy and other internal clients to ensure appropriate messaging and medium mix accomplish set marketing objectives by customer segment and therapeutic category.Manage the day-to-day follow-though of the communications agency team, ensuring deliverables are on time and adhere to the defined standards, procedures, and policies.Understand and "own" the content review and approval process and ensure that it is followed consistently. Work with all key internal stakeholders (including regulatory, legal, medical, corporate communications, and Investor Relations) to secure approval of communications pieces.Assist Marketing colleagues and agencies to develop and implement marketing communications campaigns.Serve as the primary point of contact for trade associations, industry groups, partner companies, and all marketing and promotion suppliers.Assist Marketing colleagues to develop appropriate metrics related to marketing communications programs to measure effectiveness.Ensure logistics and communications initiatives for trade shows, customer meetings, and internal meetings are developed and implemented effectively.Ensure the development and optimal use of the CRM platform to prioritize targets and identify opportunities and threats.Assist Marketing colleagues to help optimize resources, including promotional budget and team resources to maximize revenue and profitability.Participate in cross-functional team discussions for developing and implementing communications strategies that maximize growth.Provide input, share best practices, and provide feedback to Zoetis colleagues.Qualifications & ExperienceBS or BA required (Communications, Journalism, Business, or related field).5+ years of relevant marketing communications, marketing, and/or operations experience required. Pharmaceutical industry experience required. Experience working within a healthcare advertising agency as an Account Supervisor/Account Director is preferred.Must demonstrate excellent marketing communications skills and knowledge. Experience working with cross-functional teams in developing and executing segment and brand communications strategies, programs, and tactics that consistently and effectively deliver messages across brands, therapeutic areas, and customer segments in support of overall business plans.Demonstrated ability to be a team player; organize and prioritize multiple projects in a fast-paced, changing environment; and perform well and deliver high-quality under deadline.Strong computer skills (MS Office and ability to learn Zoetis systems)LocationThis position may require occasional travel for industry conferences, professional meetings, and collaboration with key stakeholders. Flexibility regarding location and the ability to work remotely or from a corporate office depending on company policy and team needs.The following base pay range reflects the anticipated base pay for this position if a selected candidate were tobe located in (Colorado). Base pay may vary based on location and other factors.Base Pay Range: $88,000 - $177,000The following base pay range reflects the anticipated base pay for this position if a selected candidate were to be located in (California), (NJ Remote), (NY Remote), or (Washington). Base pay may vary based on location andother factors.Base Pay Range: $88,000 - $177,000[This position is eligible for short-term incentive compensation.] [The position is also eligible for long-term incentive.]We offer a competitive and comprehensive benefits package, which includes healthcare, dental coverage, andretirement savings benefits along with paid holidays, vacation and disability insurance.Full timeRegularColleagueAny unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at [email protected] to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Company Description Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values of collaboration, accountability, passion, respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up their sleeves. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career. Recognitions Named Science's Top Employer in 2021, 2022, and 2023 Insmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we were named the No. 1 company to work for in the biopharma industry in Science's Top Employers Survey for two years in a row.A Certified Great Place to Work We believe our company is truly special, and our employees agree. In July 2023, we became Great Place to Work-certified in the U.S. for the third year in a row. We are also honored to have been listed on the Best Workplaces in Biopharma™, Best Workplaces in New York™, and Best Workplaces for Millennials™ lists. Overview The Director, Clinical Development will play an important role in working with the team to execute the global clinical development plans of brensocatib for the HSindication. Tasks include preparing clinical documents (e.g. protocol, study report, NDA documents), providing medical oversight for investigational sites, doing research, and participating in and providing medical/scientific leadership to study team(s). In addition, a highly strategic view is required. This opportunity will require a focus on all the clinical aspects of the upcoming HS program. Strong leadership skills are a must for this highly visible opportunity. This position will require working in a fast-paced, high energy, entrepreneurial environment. Responsibilities Additional representative responsibilities will include, but not necessarily be limited to, the following: Provides medical/scientific input and advice by working closely with Clinical Scientists and Clinical Operations personnel on clinical studies, before during and after conduct of studies, and identify/resolve issues related to study design that arise during study. Provide medical expertise where needed. Collaborate with team and CROs to prepare and finalize clinical study protocols, associated amendments and Special Protocol Assessment (SPA) Agreements in compliance with Clinical Development Plans and regulatory requirements. Provide program level medical oversight of information included in regulatory documents including clinical sections of IND submissions, IND Annual Updates / DSUR, Investigator Brochures and IMPD's Draft, briefing books, clinical sections for the NDA/CTD submissions, and responses to questions from regulatory authority or EC/IRBs. Provide medical feedback for activities related to review of data for interim analysis or blinded data reviews. Production of tables, listings and narratives of safety areas of interest/focus: eg MACE, Potential events related to metabolite, Liver enzymes. Review of mortality cases, evaluation of CIOMS, production of queries to address information gaps in CIOMS of such deaths. Review of SUSARs and contact with PIs in each reported SUSAR to understand the case assessment. Production of initial narrative to understand each individual case. Collaboration in the presentation of safety aspects in the Medical Monitoring Meeting Collaboration in Safety Management Team Provide medical/scientific review of statistical analysis. Collaborate with team in the development and implementation of Data Management activities including development of eCRFs, edit checks, coding, report development and database lock processes. Keep up to date on scientific and medical progress in the area of development and actively develops and maintain relationships with outside experts. May serve as a liaison by representing the company in outside groups. Contribute to the strategic development of early and late stage clinical programs. Qualifications Requires an MD or PharmD degree, board certified/eligible and/or specialization in Dermatology is a plus. A minimum of 5+ years of clinical development experience in the pharmaceutical/biotech Industry. Previous experience conducting clinical trials in Dermatology is a plus Working knowledge of Good Clinical Practices, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies. Must have a global perspective and mindset, with the ability to work effectively with colleagues from myriad cultures, backgrounds and geographies. Must have excellent communication skills (verbal and written). Highly organized with a strong attention to detail, clarity, accuracy and conciseness. Highly proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook). Must have strong analytical skills. Must work well both independently and in teams, have excellent time management skills and be able to work well under pressure. Travel Requirements Up to 25% travel based on vendor requirements Salary Range Insmed takes into consideration a combination of candidate's education, training, and experience as well as the position's scope and complexity, the discretion and latitude required in the role, and external market and internal value when determining a salary level for potential new employees. The base salary range for this job is from $175,000.00 to $241,667.00 per year Compensation & Benefits We're committed to investing in every team member's total well-being, now and in the future. We offer a competitive total-rewards package to all employees around the world, including: Flexible approach to where and how we work, regionally based Competitive compensation package including bonus Stock options and RSU awards Employee Stock Purchase Plan (ESPP) Flexible Vacation Policy Generous paid holiday schedule and winter break ADDITIONAL U.S. BENEFITS: 401(k) plan with company match Medical, dental, and vision plans Company-provided Life and Accidental Death & Dismemberment (AD&D) insurance Company-provided short and long-term disability benefits Unique offerings of pet, legal, and supplemental life insurance Flexible spending accounts for medical and dependent care Accident and Hospital Indemnity insurance Employee Assistance Program (EAP) Mental Health on-line digital resource Well-being reimbursement Paid leave benefits for new parents Paid time off to volunteer On-site, no-cost fitness center at our U.S. headquarters Additional Information Insmed Incorporated is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.Unsolicited resumes from agencies should not be forwarded to Insmed. Insmed will not be responsible for any fees arising from the use of resumes through this source. Insmed will only pay a fee to agencies if a formal agreement between Insmed and the agency has been established. The Human Resources department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement.Applications are accepted for 5 calendar days from the date posted or until the position is filled.#LI-JK1