Associate Director, Medical Writing — Regulatory Leader
Structure Therapeutics Inc.
Structure Therapeutics Inc. in California is seeking an Associate Director of Medical Writing to lead the development of regulatory and clinical documents, ensuring compliance with FDA, EMA and ICH guidelines, and maintaining high quality across programs. The role emphasizes cross-functional collaboration, project leadership, and QC oversight, with opportunities to mentor writers and implement best practices, templates, and processes to improve messaging and submission readiness. #J-18808-Ljbffr Structure Therapeutics Inc.
- About the job Associate Director Medical Writing Role Overview We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy...MedicalRegulatoryContract workWork at office
- Structure Therapeutics seeks an Associate Director of Medical Writing to lead development of regulatory and clinical documents for its drug pipeline, supporting cardiovascular, metabolic, and pulmonary indications. This role partners with Clinical Sciences, Regulatory Affairs...MedicalRegulatoryRemote job
$186k - $235k
...and capitalizing on the strengths of each geographic location. Position Summary The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company’s drug development programs, while...MedicalRegulatoryRemote work- ...information, please visit The Associate Director, Global Publications will play a key role within the Medical and Patient Affairs team,... ..., Translational Research, Regulatory Affairs, and Medical Affairs... ...Three to five years of medical writing, publications, or scientific...MedicalRegulatoryFlexible hours
$216.4k - $234.8k
Help shape how Nurix communicates its science to health authorities and the world. As Associate Director, Regulatory & Medical Writing, you’ll independently lead the authoring, review, and approval of critical regulatory documents across our pipeline — from clinical protocols...MedicalRegulatoryOdd jobLocal areaFlexible hoursShift work$180k - $212k
Reporting to the Vice President of Regulatory Affairs, this position is specifically responsible for the technical writing oversight of regional and/or global regulatory submissions... ..., summarize, and present statistical and medical information to ensure quality and accuracy...MedicalRegulatoryLocal areaRemote workFlexible hours$186k - $235k
Role Associate Director of Medical Writing leading the development of regulatory and clinical documents for Structure Therapeutics' drug pipeline, primarily supporting cardiovascular, metabolic, and pulmonary indications. Responsibilities authoring, reviewing, and finalizing...MedicalRegulatoryRemote work$180k - $241k
...000 employees. Job Description Primary Function: The Associate Director, Regulatory Affairs supports the development and execution of clinical... ...inputs from Clinical, Nonclinical, Biometrics, Medical Writing, CMC, and other functions. Partner with CMC Regulatory...MedicalRegulatoryRemote workWorldwideRelocation package- Structure Therapeutics Inc. is seeking an Associate Director of Medical Writing to lead regulatory and clinical document development, ensure quality and compliance, and coordinate cross-functional inputs across Clinical Sciences, Regulatory Affairs, Biostatistics, and...MedicalRegulatory
$216.4k - $234.8k
...Nurix Therapeutics seeks an Associate Director to lead regulatory and medical writing functions for clinical development programs. The role involves authoring and overseeing submission documents to health authorities, managing cross-functional teams, and ensuring content...MedicalRegulatory- Enigma Search is looking for an Associate Director, Medical Writing in South San Francisco, California. This role involves leading the development of clinical and regulatory documentation, ensuring compliance with global standards, and managing the writing process. The...MedicalRegulatory
- Nurix Therapeutics is seeking an Associate Director of Regulatory & Medical Writing to independently lead authoring, review, and approval of critical regulatory documents across our pipeline. You will drive strategic messaging, ensure document consistency, and manage the...MedicalRegulatory
- AbbVie seeks an Associate Director of Regulatory Affairs US Advertising and Promotion-Oncology to lead strategy and cross-functional teams across Medical, Marketing, Regulatory, Legal and Public Affairs. They will guide multidivisional initiatives, analyze trends, and oversee...MedicalRegulatory
- Role: Associate Director, Regional Patient Access and Experience, supporting patients, caregivers... ...with teams such as Market Access, Medical Affairs, and Patient Advocacy. The role... ...process improvements, and compliance with regulatory standards. Qualifications: Bachelor's...MedicalRegulatoryRemote work
$215k - $260k
...exciting place to catalyze and enable medical breakthroughs. Who We Are Calico (Calico... ...'s intellectual property, and ensure regulatory and corporate compliance Work... ...institutional experience with a minimum of 5 (Associate Director) or 7 (Director) years of experience in...MedicalRegulatoryContract work$141.5k - $268.5k
...issues today and address the medical challenges of tomorrow. We... ...a project and TA-level. The Associate Director, Portfolio Insights - Neuroscience... ...with ASLs (asset strategy leaders), Search & Evaluation (S&E),... ...of technical and regulatory success) for drug development...MedicalRegulatoryFull timeTemporary work$229.5k - $255.87k
...Associate Director Pharmacovigilance Operations Nurix Therapeutics is a... ...the forefront of patient care writing medicines next chapter with... ...driving in-stream quality review regulatory submission oversight... ...Management Regulatory Affairs and Medical Safety to ensure alignment...MedicalRegulatoryFull timeTemporary work$190k - $220k
...Associate Director, Device Development Marea Therapeutics... ...from interns to senior leaders. Our environment is... ...the device content of regulatory submissions. It also... ...candidate to be hands-on: writing and reviewing... ..., pharmaceutical, or medical device industry Hands...RegulatoryFull timeLocal area3 days per week$187.8k - $208.6k
Shape the CMC regulatory path for Nurix's small molecule portfolio, from clinical development... ...-functional teams, with room at the Associate Director level to own strategy and mentor... ...communication and scientific/technical writing skills Ability to manage multiple projects...RegulatoryLocal area$166k - $200k
...positions become available. Associate Director, Marketing Promotions The... ...that all activities follow regulatory, compliance and legal requirements... ..., Legal, Regulatory, Medical, Market Research, Market Access... ...of a team and expertise as a leader with well-developed influencing...MedicalRegulatory$177.91k - $230.23k
...where our business and medical science goes next.... ...employee deserves a great leader. People Leaders are... ...Affairs as an Associate Director, Medical Affairs. The... ..., Medical, Legal and Regulatory review requirements where... ...publication vendors, medical writing partners and other...MedicalRegulatoryFull timeFor contractorsLocal area- ...pipeline launches. You will own brand strategy, positioning, launch readiness, and lead cross-functional teams across Medical Affairs, Market Access, Regulatory, Sales, and Supply Chain. You will collaborate with global teams to align the U.S. #J-18808-Ljbffr Zai Lab, Ltd.MedicalRegulatoryWork at office
- Sr. Manager / Associate Director, Publications and Medical Information (Contract) Nurix Therapeutics is a clinical stage biopharmaceutical company focused... ...-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch...MedicalContract work
$171k - $223k
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated... ...oversight activities to ensure compliance with applicable regulatory requirements and company standards. Support regulatory...MedicalRegulatoryLocal area$139k - $180k
...functional collaboration and coordination with Clinical Development, Medical Affairs, Biometrics, Marketing, US & International Market... ...-based decision makers, including familiarity with the regulatory and compliance framework governing communication of such information...MedicalRegulatoryLocal area- ...information, please visit The Associate Director, Scientific Communications... ...play a key role within the Medical and Patient Affairs team,... ...medical and patient communities, regulatory authorities, investors, and... ...to five years of medical writing, publications, or scientific...MedicalRegulatoryFlexible hours
$180k - $200k
...address serious diseases with high unmet medical need. Our pipeline is anchored by T‑... ...Biotherapeutics is seeking an Associate Director of Clinical Supply Chain to plan and deliver... ...Operations, Technical Operations, Quality, Regulatory Affairs, and external vendors to keep...MedicalRegulatoryContract workWork at office2 days per week3 days per week$146k - $182.5k
...office three days per week on average. Position Summary The Associate Director, Regulatory Operations provides leadership for global regulatory... ...Competitive base, bonus, new hire and ongoing equity packages Medical, dental, and vision insurance Employer‑paid life,...MedicalRegulatoryFor contractorsWork at officeLocal areaRemote workNight shift3 days per week$90 - $98 per hour
...Description Job Title: Global Clinical Trial Leader Location: South San Francisco, CA Type... ...of GCP/ICH requirements, international regulatory guidelines, and drug development... ...welfare benefits coverage options including medical, dental, vision, spending accounts, life...MedicalRegulatoryContract workLocal areaFlexible hours$120.2k - $223.2k
The Position Commercial Regulatory Affairs (CORA) is part of the Global Product and Access Legal (GPAL) organization... ...of GPAL in the Global Legal Pharma Department. Associate Program Directors of Commercial Medical Legal Regulatory Review Committees (CMLRs) provide regulatory...MedicalRegulatoryWork experience placementLocal areaWorldwideRelocation package
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