Associate Director Of Regulatory Affairs
Green Key Resources
Job DetailExperience Level Associate DirectorDegree Type Bachelor of Arts (BA)Employment Full TimeWorking Type HybridJob Reference 0000021202Salary Type AnnuallyIndustry PharmaceuticalsSelling Points Lead impactful regulatory projects ensuring compliance with FDA standards. Collaborate across departments to streamline processes and drive innovation. Hybrid work arrangement offering flexibility and growth opportunities.Job DescriptionAssociate Director of Regulatory Affairs OverviewThe Associate Director of Regulatory Affairs will oversee advertising and promotional compliance for pharmaceutical products.Provide strategic regulatory advice for product communication and disease area initiatives.Collaborate with cross-functional teams including Marketing, Legal, and Medical Affairs to ensure compliance.Maintain up-to-date knowledge of FDA regulations and industry standards.Lead efforts to streamline review processes and minimize complexity.Serve as the primary contact for FDA’s Office of Prescription Drug Promotion (OPDP).Develop and deliver training on FDA advertising and promotion regulations.Contribute to health authority negotiations and ensure accurate submission of promotional materials.Hybrid work arrangement offering flexibility and professional growth opportunities.Associate Director of Regulatory Affairs Key Responsibilities & DutiesReview and provide oversight for product and disease state education materials.Ensure alignment with FDA regulations and approved labeling standards.Participate in multidisciplinary teams such as Copy Clearance and Global Regulatory Teams.Establish and revise procedures to maintain compliance with advertising and promotion requirements.Build and maintain strong relationships with internal stakeholders.Provide training and guidance on FDA regulations to employees and agents.Shape strategies based on emerging trends and regulatory updates.Lead efforts to simplify and enhance review processes for promotional materials.Submit promotional materials to FDA under Form FDA-2253 accurately and promptly.Associate Director of Regulatory Affairs Job RequirementsBachelor’s degree in a health or science-related field; advanced degree preferred.Minimum of 7 years of experience in Regulatory Advertising and Promotion Review.High-level knowledge of FDA laws, regulations, and industry standards.Strong understanding of clinical trial design and data interpretation.Excellent interpersonal and communication skills, both written and verbal.Ability to negotiate business decisions and drive compliance solutions.Travel up to 20% may be required for the role.Proven ability to communicate complex issues clearly and concisely.Experience in leading cross-functional teams and regulatory projects.
- ...Associate Director of Regulatory Affairs CMC Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health Authority submissions, collaborating...Suggested
$167.65k - $207.1k
...Associate Director, Regulatory Operations Waltham, Massachusetts, United States Nearly 37 million Americans are currently affected by Chronic... ...processes, standards, and systems that enable Regulatory Affairs to operate effectively. The successful candidate will...SuggestedWork at office$150k - $200k
...The Associate Director, Advertising and Promotion Compliance, US will serve as the Regulatory Affairs (RA) representative for assigned products and therapeutic areas. They will be responsible for reviewing and approving the regulatory content of materials created for...SuggestedTemporary workWork at officeFlexible hours3 days per week- ...ScholarRock on X and on LinkedIn. Summary of Position: The Associate Director, Regulatory Strategy, is responsible for the development and... ...matter expert, this individual will represent regulatory affairs at the appropriate program team, highlighting risks and opportunities...SuggestedShift work
$135.3k - $202.9k
...culture, presenting great opportunities for personal development and career advancement across the globe.Scope: The Associate Director, Global Regulatory Affairs Lead is responsible for the regulatory strategy and execution for their assigned projects in their region /...SuggestedLocal areaRemote workMonday to FridayFlexible hours$161.6k - $242.4k
Job DescriptionGeneral Summary:The Regulatory Labeling Associate Director will be responsible for strategic labeling and for executing on one or more... ...fieldTypically requires 8 years of experience in regulatory affairs in the area of global labeling or related discipline,...Full timeSummer workWork at officeRemote workFlexible hours2 days per week- ...help them achieve their goals.Job DescriptionReporting to the Director of the Office for Community Support, Non-Discrimination, Rights... ...(CSNDR) and University Title IX Coordinator, the Associate Director for Compliance and Title VI Coordinator is responsible...Work at officeLocal area
$160.1k - $286k
...adoption, and outcomes; the AI TO provides the rigor, expertise, visibility, and support required to accelerate progress. The Associate Director role will work closely with functional leaders, business owners, Finance, Data, Technology, HR, and other stakeholders to...Full timeWork at officeImmediate startRemote work- A prestigious educational institution is seeking an Associate Director for Compliance and Title VI Coordinator. This role involves oversight of compliance with Title VI, managing Title IX hearings, and supervising a compliance team. Candidates must have a J.D. and significant...
$194k - $237k
...patients we serve.Position Summary: The Associate Director, Medical Review & Training serves as... ...training in conjunction with the medical affairs leadership team (MALT). Additionally,... ...understanding of medical, legal, and regulatory review processesExcellent cross-...Full timeFlexible hours$150k - $200k
...LinkedIn and Facebook.Role Summary:The Associate Director, Medical Information and Review plays... ...readiness. This role serves as a key Medical Affairs partner in the review of promotional... ..., and alignment with applicable regulatory, legal, compliance, and company standards...Local area- ...patients in single agent and combination dosing. The Role:The Associate Director, Translational Medicine plays a critical role in both... ...CROs to ensure protocols are followed, and contribution to regulatory documentsAnalyze, interpret and report results of clinical biomarker...Temporary workWork at officeLocal areaImmediate start
- ...Job Description Job Description Associate Director, Regulatory Affairs Location: Boston, MA (Hybrid or East Coast, USA) Employment Type: Full-time, Permanent About the Company Our client is a growing consultancy supporting innovative biotechnology and pharmaceutical...Permanent employmentFull time
$170k - $195k
...For more information, visit or follow us on LinkedIn. What's the opportunity? We are seeking a highly skilled Associate Director, Regulatory Affairs to support and help drive regulatory success and shape the development of life-changing treatments. In this role, you...Work experience placementShift work$170.9k - $231.3k
...Overview The Associate Director of Regulatory Affairs Strategy will work on assigned programs with the respective Global Regulatory Portfolio Lead, Global Regulatory Lead and cross-functional team to lead and define the regulatory strategy, facilitate submission...Full timeTemporary workLocal areaWorldwideFlexible hours2 days per week- ...The Associate Director of Regulatory Affairs CMC will be responsible for developing, implementing and advising on global Regulatory CMC strategies for new and late stage programs to secure approval of the manufacturing process and control testing for initial clinical...
$182k
...Instagram ( , X ( and YouTube. ( Job Description The Director Regulatory Affairs Global Regulatory Lead (GRL II), Global Regulatory... ...participating in and taking leadership roles in professional associations, industry, and trade groups as appropriate for assigned projects...Local areaWorldwide- ...Zugo-cel CAR-T franchise at CRISPR. Reporting to the Head of Regulatory Affairs, you will work closely with cross-functional teams and... ...demonstrated track record of significant accomplishments: ~ Associate Director: ~12+ Years of relevant experience with a bachelor's...Contract workRemote work
- ...meet the business needs. Deep understanding of assay design, regulatory standards and industry best practices are essential. The incumbent... ..., regulatory expectations, clinic/submission readiness and associated risks. Research and Development Ensure the timely...Work experience placement
$175.35k - $219.2k
...About the Job: The Associate Director, Regulatory Affairs is responsible for supporting the regulatory function and its activities, the development of regulatory strategy, and contributing the regulatory approval process (including US FDA and other regulatory authorities...- ...seeking a highly motivated and experienced Associate Director, Biostatistics to play a critical role... ...to influence clinical trial design, regulatory strategy, and corporate milestones.... ...Operations, Data Management, Regulatory Affairs, and Investor Relations. Maintain...Work at office3 days per week
- ...leading biotech company in Cambridge, MA, seeks an experienced Associate Director of Regulatory Strategy to lead oncology therapeutic programs. This role requires extensive experience in regulatory affairs, particularly in oncology, to ensure alignment between US and global...
- .... Summary of Position: Scholar Rock is looking for an associate director level subject matter expert to build clinical operations compliance... .... Partner with cross-functional team members within Regulatory, Quality, Data Sciences, Clinical Research,...Work at officeFlexible hours
- ...Instagram , X and YouTube. Job Description The Associate Scientific Director, Medical Affairs, plays a key role in advancing medical affairs... ...established policies and practice standards, including regulatory guidelines, to meet customer needs. Contributes to...Full timeWork at officeLocal area
$167k - $286k
...Lexington, Massachusetts, United StatesSalary: $167,000 - $286,000Company: Wave Life SciencesPosted: Director/Associate Director, Platform and Pipeline Medical Affairs LeadWave Life Sciences is a biotechnology company focused on unlocking the broad potential of RNA medicines...Contract workTemporary workSummer workWork at officeLocal area$184.78k - $205.78k
...Associate Director (AD), Medical Information & Review The Associate Director (AD), Medical... ...position is within the Alkermes Medical Affairs department and will report to the Director... ...with reviewer colleagues in Regulatory and Legal functions to provide expert...Full timeLocal areaShift work- ...Associate Director, Medical Affairs (Transplant and Immunology) CSL's organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic...Work at officeWorldwide3 days per week
$184.07k - $198.8k
The Associate Director of Statistical Programming, as a member of the Biostatistics & Statistical Programming Department, will contribute to... ...-house and outsourced projects in CDISC compliance to meet regulatory requirements. In addition, this individual will support the...Work at officeLocal areaFlexible hours3 days per week- ...visit us at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description Purpose: As Associate Director, AI Strategy and Planning, you are responsible for driving AI strategy and governance across Operations and ensuring...Full timeLocal area
- Treeline in the United States is seeking an experienced Associate Director / Director of Regulatory Affairs to lead global regulatory activities and ensure compliance with applicable laws and guidelines. This hands-on role will influence regulatory strategy, prepare and...
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