Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Senior Nonclinical Medical Writer: Lead Preclinical Submissions

MSD Malaysia

Merck & Co., Inc. seeks an experienced Medical Writer to join the Nonclinical Pharmacology Documentation group. You will generate preclinical reports and regulatory submission modules, partnering with research and regulatory teams to ensure high-quality scientific and regulatory documents across multiple programs. The role requires managing multiple programs, prioritizing timelines, and driving completion in alignment with regulatory milestones. #J-18808-Ljbffr MSD Malaysia

Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Senior Nonclinical Medical Writer: Lead Preclinical Submissions in South San Francisco, CA vacancy
  • Merck & Co., Inc. in California seeks an experienced Medical Writer to join our Nonclinical Pharmacology Documentation group, managing multiple preclinical programs and regulatory modules. You will collaborate with research and regulatory teams to produce high-quality... 
    Senior

    MSD

    South San Francisco, CA
    2 days ago
  • Denali Therapeutics Inc. in South San Francisco seeks an Associate Director in Toxicology to lead nonclinical safety strategies for multiple programs. You will play a key role in interpreting complex data and influencing program decisions that ensure patient safety and... 
    Senior

    Denali Therapeutics Inc.

    South San Francisco, CA
    3 days ago
  • Veratherapeuticsinc seeks a Senior Manager, Regulatory CMC to manage regulatory submissions and activities within a dynamic team...  ...organizational skills, and the ability to lead cross-functional projects....  ...options, and comprehensive medical benefits. #J-18808-Ljbffr Veratherapeuticsinc
    Senior

    Veratherapeuticsinc

    Brisbane, CA
    3 days ago
  • BridgeBio seeks a Senior Manager / Associate Director, CMC Regulatory Sciences in the San Francisco area for a hybrid role. The candidate...  ...to design control strategies, author and review regulatory submissions, and respond to health authority queries to support global... 
    Senior

    BridgeBio

    San Francisco, CA
    1 day ago
  • The Associate Director Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) leads initiatives to develop and manage regulatory strategies for CMC submissions, including INDs/CTAs and amendments. This role builds relationships across Regulatory Affairs, Operations... 
    Senior

    Allergan

    South San Francisco, CA
    3 days ago
  • Penfield Search Partners Ltd is seeking a Senior Regulatory Submission Lead to drive a BLA submission across Module 2 and Module 5 for a Bay Area-based project. This 1-year contract role emphasizes hands-on submission execution, cross-functional coordination, and regulatory... 
    Senior
    Contract work

    Penfield Search Partners Ltd

    San Francisco, CA
    3 days ago
  • $120 - $175 per hour

     ...penfieldsearch.comNo 3rd party candidatesLocation: Bay Area-based roleWork Model: 5 days onsite per weekWe are seeking a Senior Regulatory Submission Lead to support a critical BLA submission across Module 2 and Module 5. This 1 year contract role will provide hands-on... 
    Senior
    Hourly pay
    Contract work

    Penfield Search Partners Ltd

    San Francisco, CA
    3 days ago
  • Position Title: Senior Medical Content Writer Work Location: South San Francisco, CA Assignment Duration: 3 Months Work Schedule: Monday through...  ...and claim substantiation packages ready for MLR submission. Write medical content across formats: HCP materials, patient... 
    Senior
    Work at office
    Monday to Friday

    Spectraforce Technologies

    South San Francisco, CA
    5 days ago
  • $182.1k - $338.3k

     ...world where we all have more time with the people we love. Medical Operations Education & Communication (MOEC), a function in...  ...accessible and affordable for all.The Principal Content & Evidence Submission Strategy Lead is focused on developing the medical communications... 
    Full time
    Local area

    Genentech

    South San Francisco, CA
    3 days ago
  • $171k - $223k

     ...level Toxicologist with over 10 years of industry experience to lead nonclinical safety strategies across discovery and development stages....  ...mentoring junior scientists, providing input on regulatory submissions, and developing innovative toxicology processes. We offer a... 
    Senior

    Denali Therapeutics Inc

    South San Francisco, CA
    4 days ago
  •  ...hours/week) to manage a variety of writing and editing projects, including Clinical Study Protocols, amendments, CSRs, regulatory submissions and DSUR responses. The role requires extensive experience in clinical/regulatory writing within biotech, strong communication... 
    Remote job
    Contract work
    Part time
    For contractors

    Redbock - an NES Fircroft company

    San Francisco, CA
    2 days ago
  • $131.4k - $206.8k

    Job Description We are seeking an experienced Medical Writer to join our Nonclinical Pharmacology Documentation group responsible for the generation of preclinical reports and submission modules to support development programs ranging from FIH to global marketing applications... 
    Senior
    For contractors
    Work at office
    Local area

    MSD Malaysia

    South San Francisco, CA
    2 days ago
  •  ...Therapeutics in South San Francisco seeks an Associate Director, CMC Program Management to lead CMC strategies, deliverables, and timelines across development stages, including NDA/MAA submissions. You will manage CRO/CMO vendors and guide cross-functional teams to integrate CMC... 
    Senior

    Denali Therapeutics

    South San Francisco, CA
    2 days ago
  • Genentech in South San Francisco, CA, seeks a Medical Operations Education & Communication (MOEC) leader to drive U.S. content strategy, align with medical priorities, and guide evidence submission to support patient access. The role requires an advanced clinical or science... 
    Senior

    F. Hoffmann-La Roche AG

    South San Francisco, CA
    5 days ago
  • A leading biopharmaceutical company in South San Francisco seeks a Senior Bioanalytical Scientist to design and execute bioanalytical strategies for discovery and preclinical development. The role involves developing bioanalytical methods for small molecules and antibody... 
    Senior

    Sutro Biopharma

    South San Francisco, CA
    5 days ago
  •  ...pharmacology and regulatory, and driving data-driven decisions. You will oversee in vitro and in vivo ADME/PK studies, translate data into human PK predictions, manage risk mitigation, and contribute to regulatory submissions and IND/NDA support. #J-18808-Ljbffr Genentech
    Senior
    Relocation

    Genentech

    South San Francisco, CA
    4 days ago
  • Spectraforce Technologies is seeking a Senior Medical Content Writer in South San Francisco, CA. The role is hybrid (Tue-Wed-Thu in office) with a 3-month assignment. You will craft, substantiate, and annotate claims for pharma content, working inside an in-house studio... 
    Senior
    Work at office

    Spectraforce Technologies

    South San Francisco, CA
    5 days ago
  • $244k - $305k

     .... The Opportunity: The Senior Director, Molecule Global Regulatory Lead will develop and execute...  ...teams. Regulatory Submission Leadership Provide strategic...  ...Regulatory Operations, Medical Writing, Clinical...  ...Clinical Operations, Safety, Nonclinical, CMC, Biometrics,... 
    Senior
    Full time
    Local area

    Revolution Medicines

    San Francisco, CA
    5 days ago
  • $186k - $233k

     ...experienced Statistical Programmer with over 14 years in oncology trials. The role entails leading studies, collaborating with teams, and overseeing programming support for regulatory submissions in a dynamic environment. This opportunity offers competitive pay, from $186,000... 
    Senior

    REVOLUTION Medicines

    San Francisco, CA
    2 days ago
  •  ...This role involves developing and implementing project plans, ensuring regulatory strategy execution, and overseeing regulatory submissions both pre- and post-approval. Candidates should have a minimum of 8 years in regulatory development within the pharmaceutical industry... 
    Work at office

    Acadia Pharmaceuticals

    South San Francisco, CA
    4 days ago
  •  ...Therapeutics, based in South San Francisco, seeks a Senior Manager, Regulatory Affairs to lead regulatory planning and tactical execution for US and...  ...coordinating with internal teams and external partners to drive submissions and regulatory strategy. The ideal candidate has >8... 
    Senior

    BioSpace

    South San Francisco, CA
    2 days ago
  •  ...We are partnering with a growing organization seeking an experienced Senior Payroll Lead to take ownership of its payroll function. This is a senior-level, hands-on role with responsibilities comparable to a Payroll Manager, but structured as an individual contributor... 
    Senior
    Local area

    3 Bridge Networks

    Burlingame, CA
    8 hours ago
  •  ...Project Manager to oversee project management of drug development processes. Responsibilities include leading cross-functional teams, managing regulatory submissions, and ensuring projects meet business needs. Ideal candidates will possess strong leadership, project management... 
    Senior

    Mindlance

    South San Francisco, CA
    5 days ago
  •  ...across a portfolio of neurodegenerative disease programs. You will partner with Regulatory Affairs, Medical Writing, Operations, and development SMEs to ensure submissions stay on track and aligned with program goals. The role emphasizes proactive risk identification,... 
    Senior

    Denali Therapeutics Inc

    South San Francisco, CA
    2 days ago
  • YO AI Labs seeks an experienced Medical Writer Expert for remote contract work. You will develop, review, and evaluate clinical and regulatory documents with a focus on accuracy, regulatory compliance, and quality. This role requires deep expertise in CSRs, ICH guidelines... 
    Senior
    Remote job
    Contract work

    YO AI Labs

    San Francisco, CA
    3 days ago
  • $154.89k - $176.98k

     ...therapies for people with unmet medical needs. Since 2004,...  ...Statement The mission of the Preclinical Development team is to attract...  ...therapeutic candidates toward IND submission and clearance Experience...  ...Supervision Received The Senior Science Officer I reports directly... 
    Senior
    Casual work
    Work at office
    Remote work

    CIRM

    South San Francisco, CA
    2 days ago
  • Mill is seeking an experienced Sustaining Program Manager to own the day-to-day program management of Mill's Consumer hardware line as it scales from launch into steady-state production. You will drive sustaining engineering, supply chain activities end to end, engineering...
    Senior

    Socket.dev

    San Bruno, CA
    3 days ago
  • Structure Therapeutics Inc. is seeking a Senior/Program Manager to serve as the execution engine for late-stage clinical programs. You will manage timelines, risks, and communications to ensure milestones are met on time and within budget, collaborating across a global... 
    Senior

    structuretx

    South San Francisco, CA
    5 days ago
  • Genentech in South San Francisco, CA is seeking a highly motivated scientist to lead pharmacology efforts within the CVRM Translational Biology group. The role focuses on driving drug discovery and mechanistic studies, coordinating multidisciplinary teams to advance candidates... 
    Senior

    Genentech

    South San Francisco, CA
    2 days ago
  • Lvi-Associates is seeking a Senior Construction Manager for Life Science projects in South San Francisco, CA. You will lead a team of architects, engineers, consultants, and contractors through strategy, design, and construction of novel facilities and tenant improvements... 
    Senior
    For contractors

    Lvi-Associates

    South San Francisco, CA
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Senior Nonclinical Medical Writer: Lead Preclinical Submissions. Be the first to apply!