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  • Associate Director, GCP/GLP/GVP QA

    $160k - $240k

     ...to overcome barriers, together. Opportunity Overview As the Associate Director, GCP/GLP/GVP QA, you will oversee GCP activities, ensure compliance and quality execution of clinical studies. You will assist in the development and management of GCP quality processes... 
    Suggested
    Full time
    Contract work
    Work at office
    Immediate start
    Night shift

    Rhythm Pharmaceuticals

    Boston, MA
    a month ago

  • Global Study Associate Director

    $137.94k - $206.91k

     ...Job Title: Global Study Associate Director Location: Durham, NC Introduction to role: Are you ready to lead global clinical studies that turn cutting-edge science into evidence that changes patients’ lives? In this role, you will own the end-to-end delivery... 
    Suggested
    Hourly pay
    Contract work
    Temporary work
    Work at office
    Flexible hours
    3 days per week
    Durham, NC
    15 days ago

  • Local Study Associate Director- FSP

     ...This is a remote role. Oncology experience is required for this role and cell therapy is strongly preferred! The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to... 
    Suggested
    Local area
    Remote work
    Flexible hours
    Remote
    more than 2 months ago

  • Associate Director, Study Feasibility & Clinical Partnerships

    $120k - $160k

     ...more accessible for all. To learn more about Care Access, visit  How This Role Makes a Difference Reporting to the Sr. Director of Study Feasibility & Clinical Partnerships, the Associate Director and Director of Study Feasibility & Clinical Partnerships provides... 
    Suggested
    Full time
    Temporary work
    Work at office
    Local area
    Remote work
    Worldwide
    Visa sponsorship
    Work visa
    Flexible hours

    Care Access

    Boston, MA
    9 days ago

  • Executive Director, HR Operations & Business Partnership

     ...Executive Director, HR Operations & Business Partnership About the Company Dynamic pharmaceutical company...  ...laboratory analytical services toxicology study cdmo safety pharmacology preclinical study glp / non-glp study ind-enabling nda submission... 
    Suggested

    Confidential

    Overland Park, KS
    2 days ago

  • Clinical Study Associate Manager

    $109.9k - $179.3k

     ...Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Associate Manager to join our Clinical Trial management team. In this role, you will support the Clinical Study Lead by taking... 
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    Contract work
    Worldwide

    Regeneron

    New Jersey
    more than 2 months ago

  • Director of Study

    We are looking for a Director of Study for an International School based in Guangzhou. This position is available from the upcoming 2026-2027 academic year, commencing in August 2026.About the schoolLocated in Guangzhou’s Panyu district, this bilingual school offers a unique... 
    Suggested
    Full time
    Summer work

    China Global Connections

    China
    more than 2 months ago

  • Study Director

     ...CDMO, advanced material sciences and in the support of clinical studies.Job DescriptionSupervise and assist in the conduct of regulatory...  ...development, design and implementation.Responsibilities as stated in GLP regulations.Data interpretation and report writing.Client... 
    Suggested
    Full time
    Monday to Friday

    Eurofins

    New Jersey
    3 days ago

  • Study Director - Americas CRO

     ...apply.  Argenta is currently looking to fill the role of Study Director   at our Oakland, NE  location.  Key Responsibilities...  ...but retails full responsibility Ensures the study follows GLP and study protocol, overseeing animal care, sample collection... 
    Suggested
    Contract work

    Argenta

    Oakland, NE
    8 days ago

  • Study Director II

     ...Job Description Job Description Study Director – Non-Human Primate Research Program Location: Corpus Christi, Texas Job Type:...  ...with an emphasis on sponsor-facing roles. ~ Familiarity with GLP/GCP environments is an asset, however, at this time the facility... 
    Suggested
    Full time
    Weekend work

    RPM ReSearch

    Corpus Christi, TX
    17 days ago

  • Study Director

     ...Job Description Job Description Join Our Team as a Study Director and Research Scientist! Your New Opportunity: We're all about teamwork...  ..., documentation, and reporting of study results for both GLP and non-GLP studies. What You’ll Do: Oversee the technical... 
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    For subcontractor

    RPM ReSearch

    West Sacramento, CA
    28 days ago

  • Associate Director Toxicology

    $155k - $193.2k

     ...average. Position Summary The Associate Director will be responsible for the oversight of...  ...overseeing preclinical safety and toxicology studies in support of diverse projects and long‑...  ...experience on Good Laboratory Practices (GLP) safety assessment/toxicology studies at... 
    Suggested
    Work at office
    Local area
    Remote work
    Night shift
    3 days per week

    ACADIA Pharmaceuticals

    San Diego, CA
    1 day ago

  • Associate Director, Toxicology

     ...highly motivated and experienced Associate Director of Toxicology (Nonclinical Safety) to...  ...candidate selection and overall program strategy Study Design & Execution Design, oversee, and...  ...studies, including: Exploratory/non-GLP toxicology studies IND-enabling toxicology... 
    Suggested

    Latigo Biotherapeutics, Inc.

    San Francisco, CA
    3 days ago

  • Associate Director, Toxicology

    $185k - $205k

     ...Associate Director, Toxicology, Nonclinical Development (Program Toxicologist) Position Description: Protagonist Therapeutics...  ...developing nonclinical toxicology strategies, overseeing GLP and non-GLP studies, preparing toxicology components of regulatory submissions,... 
    Suggested
    Worldwide
    Flexible hours

    Protagonist Therapeutics

    Newark, CA
    1 day ago

  • Associate Director, Toxicology

    $170k - $210k

     ...Associate Director, Toxicology Parabilis Medicines is seeking a highly motivated and driven...  ..., design early safety profiling studies, and guide candidate selection through science...  ...and specialty contract laboratories for GLP and non-GLP preclinical studies. Review... 
    Suggested
    Contract work
    Interim role
    Local area
    Shift work

    Parabilis Medicines

    Cambridge, MA
    20 hours ago

  • Associate Director OF Project Management

    $155.7k - $233.5k

     ...Description****General Summary:**The Associate Director, Preclinical Sciences, Program Management...  ...high-level professionals* May serve as study representative on preclinical studies.*...  ...*** Broad and comprehensive knowledge of GLP regulations* Comprehensive knowledge of... 
    Contract work
    Work experience placement
    Summer work
    Remote work
    Worldwide
    Flexible hours
    2 days per week

    Vertex Pharmaceuticals

    Boston, MA
    4 days ago

  • Associate Director, Assay and Process Development

    $120k - $150k

     ...the Chief Science Officer, the Associate Director, Assay and Process Development works within...  ...from conception to production for GLP level pre-clinical test products. Responsibilities...  ...Design, Design of Experiment statistical studies to identify controlling and interacting... 
    Contract work

    Celcuity

    Minneapolis, MN
    23 days ago

  • Associate Director Quality Assurance

     ...sciences and in the support of clinical studies, as well as having an emerging global presence...  ...US Food laboratory. The Associate Director of Quality Assurance will be responsible...  ...participation and contributions Applies GMP/GLP in all areas of responsibility, as... 
    Full time
    Contract work
    Local area
    Weekend work

    RXinsider

    Madison, WI
    20 hours ago

  • Scientist/ Study Director Toxicology - Preclinical CRO

     ...Job Description Job Description Senior Study Director/ Toxicologist We are a growing mid-size organization with multiple sites looking...  ..., good organizational skills, knowledge of an experience with GLP (Good Laboratory Practices), AAALAC and USDA guidelines,... 

    RPM ReSearch

    Columbia, MO
    5 days ago

  • Associate Director, Bioanalytics

     ...Job Description Job Title: Associate Director, Bioanalytics Location: Thousand Oaks...  ...and sample analysis activities. Review study plans, protocols, validation reports, and...  ...activities are conducted in accordance with GLP, GCP, and applicable regulatory guidance.... 

    Latigo Bio

    San Francisco, CA
    7 days ago

  • Associate Director, Process Chemistry

    $200k - $220k

     ...are seeking an experienced and highly motivated Associate Director of Process Chemistry to manage and drive drug substance process...  ...solving to ensure on-time supply of drug to support non-GLP toxicology studies, IND-enabling activities, and clinical trials across multiple... 
    Full time
    Contract work

    Septerna

    South San Francisco, CA
    9 days ago

  • Associate Scientific Director Laboratory Sciences Bioanalysis

    $145k - $150k

     ...scientific and operational processes for discovery through regulated (GLP) and clinical bioanalytical services. Manage assigned scientific...  ...with providing costing estimates for components of applicable studies.  • Lead implementation of new procedures and refinement of... 
    Contract work
    Work at office
    Local area
    Worldwide
    Flexible hours

    Charles River Laboratories, Inc.

    Reno, NV
    more than 2 months ago

  • Associate Director, Analytical Development and Clinical QC

     ..., Q6B, Q8-Q12), USP/EP, FDA/EMA expectations for biologics, GMP/GLP compliance, and authoring/reviewing CTD Module 3, IND/IMPD, BLA/...  ...characterization and comparability including forced degradation studies for process comparability. Familiarity with LIMS, ELN, Chromatography... 
    Work at office
    Flexible hours
    Shift work
    New Haven, CT
    more than 2 months ago

  • Associate Director, Drug Product Development

    $165k - $205k

    The Associate Director of Drug Product Development supports the planning and execution of the...  ...assessments, and forced degradation studies. Supervise CDMO to execute formulation...  ...preferred. Extensive knowledge of cGMP, GLP, ICH guidelines, FDA regulations, and other... 
    Full time
    Remote work
    Work from home
    Flexible hours
    Night shift
    Afternoon shift
    Early shift

    Syncromune

    Fort Lauderdale, FL
    a month ago

  • Associate Director, Study Feasibility

     ...visit us at  . Follow @abbvie on  LinkedIn,   Facebook ,  Instagram ,  X and  YouTube. Job Description As a Study Feasibility Associate Director, you will be part of AbbVie’s Clinical Development Operations (CDO) function, which is responsible for running... 
    Full time
    Local area

    AbbVie

    Illinois
    12 hours agonew

  • Associate Director, Study Manager, Immunology

    $142.4k - $224.1k

     ...feasibility, execution and conduct of clinical trial(s) Serves as the Clinical Trial Team lead Leads and directs teams in key study planning, development, and execution elements (e.g. operational reviews, issue escalation/mitigations, presentations at Sr Management... 
    Full time
    For contractors
    Work at office
    Local area
    Relocation
    Visa sponsorship
    Flexible hours
    Shift work

    Merck & Co.

    San Diego, CA
    2 days ago

  • Human Resources Director

    $1,000 per month

     ...Public Utility Authority seeks an experienced Human Resources (HR) Director to lead the organization’s HR strategy and oversee a variety of...  ..., management, business administration or any related course study. Seven (7) years of professional work experience including... 
    Work experience placement
    Zero hours contract
    Work at office
    Local area
    Shift work

    Cape Fear Public Utility Authority

    Wilmington, NC
    12 days ago

  • Associate Director of Clinical Pharmacology

    $120k - $156k

     ...Pharmaceutical Sciences to be Associate Director of Clinical Pharmacology. This role is designed...  ...interpretation of clinical pharmacology studies (Phase I–III), develop and implement...  ...bioanalytical, pharmacology, and non-GLP safety assessments. We are also a drug development... 
    Full time
    Contract work
    Work at office
    Local area
    Remote work
    Worldwide
    Visa sponsorship
    Work visa

    Xyzagen

    Pittsboro, NC
    7 days ago

  • Senior Director, Oncology Pharmacology

    $232k - $348k

     ...and governance-level teams. Collaborate with CROs to outsource studies, develop protocols, manage timelines and budgets, and partner...  ...multiple complex pharmacology programs at diverse CROs, including GLP and non-GLP environments. Expertise designing and executing... 
    Remote work
    Flexible hours

    Jazz Pharmaceutical

    United States
    2 days ago

  • Associate Director, Medical Affairs

     ...meaningful difference worldwide. Could you be our next Associate Director, Medical Affairs (Immunology)? The job is in our King of...  ...patient advocacy groups. Supports coordination of investigator led studies and research collaborations Serves as scientific consultant... 
    Work at office
    Worldwide
    3 days per week

    CSL

    King of Prussia, PA
    20 hours ago