Associate Director, Clinical Pathologist
$176.1k - $287.3kRegeneron Pharmaceuticals, Inc.
Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Clinical Pathology support to selected TFAs, and mentor junior Pathologists.
A Typical day in this role may look like:
Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas.
Work both independently and as a part of integrated discovery and development teams to interpret pharmacologic and toxicity related findings and help advance promising therapeutics through Regeneron’s pipeline.
Determining and evaluating clinical pathology-related endpoints in pharmacology and toxicology studies and guiding decision making.
Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron.
Partner with our CRO partners in providing scientific peer review of nonclinical safety studies.
This job might be for you if you have:
Experience with integrating clinical and anatomic pathology data
Experience with animal models of human diseases
Clear, concise oral and written communication skills
Demonstrated ability to contribute to cross functional teams
Ability to contribute to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes.
In order to be considered for this role, you must have :
- DVM (or equivalent) with ACVP certification in Clinical Pathology required, (strong preference for PhD in Pathology, Immunology, or related )
- Minimum 3 years of industry experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/ biotech or CRO setting.
- Additional certification in Anatomic Pathology nice to have
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$176,100.00 - $287,300.00- ...Schedule: Full time Weekly Hours: 40.00 Job Summary The Associate Laboratory Director will collaborate with the Director of Operations and any... ...supervise the development and implementation of complex clinical molecular assays, introduction of new technologies, participate...SuggestedFull timePart timeWork from homeShift workDay shift
$158.6k - $285.5k
The Role This role will support Oncology Therapeutic programs, specifically supporting the Clinical Study Lead in the development, execution and evaluation of Phase 1-3 clinical studies. The principal responsibility for this role is to ensure the comprehensive data quality...SuggestedPermanent employmentFull timeWork at officeWork from home$175k - $200k
...ApplicationsEmail: ****@*****.*** include: Accountable for the oversight and execution of multiple clinical trials including: Develop, implement, and provide oversight of vendor budgets and contracts Tracking and reporting of study...SuggestedContract workRemote work- ...CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial... ..., plus equity grants which have become very lucrative for our associates.ResponsibilitiesManage and provide accountability for day-to-day...SuggestedContract workWork from home
$150k - $195k
Department:107600 Clinical PharmacologyLocation:San Diego, USA- RemoteBe a part of a global team that is inspired to make a difference... ...science and service for rare patients.Position Summary:The Associate Director, Clinical Pharmacology will be responsible for the design,...SuggestedFull timeTemporary workRemote workShift work$173.22k - $209.9k
...make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: The Associate Director of Clinical Science plays a supportive role in clinical development of RazyeBio radiopharmaceuticals for oncology indications....Hourly payFull timeContract workTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaImmediate startRemote workFlexible hours$169.5k - $203.25k
Introduction:Xencor is a public, clinical-stage biopharmaceutical company located in the Los Angeles area (Pasadena) and in San Diego... ..., please visit We have an excellent opportunity for an Associate Director, Clinical Trial Management with experience in Autoimmune diseases...Full timeWork at officeRemote work2 days per week$154.4k - $242.55k
...looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Director, Clinical Pharmacology in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven...Minimum wageFull timeContract workWork at officeLocal areaRemote work$130k - $200k
...Associate Director, Clinical Pharmacology Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our...Remote work$150k - $187k
...Job Description Associate Director, PBM Clinical Services (PharmD)- Hybrid (Denver, CO) HealthCare Support is seeking an Associate Director, PBM Client Services to be part of an Enterprise Health Technology company , giving health plans a better way to manage...Work at officeLocal areaImmediate startRemote workMonday to Friday$180k - $210k
...Jeffery W. Kelly and Dr. Richard Labaudinière, for the treatment of transthyretin amyloidosis. About the job The Associate Director (AD), Clinical Operations will be responsible for independently managing the operational execution of assigned clinical trials,...Full timeContract workRemote workRelocation packageMonday to Friday$186k - $220k
...limitations of biologic and peptide drugs. We are advancing a clinical‐stage pipeline of differentiated treatments focused on... ...strengths of each geographic location.Position Summary:The Associate Director of Clinical Operations plays a pivotal role in leading clinical...Contract workRemote work$164k - $213k
...the UK.For patients, for each other, and for the future of science, we’re in. Are you?About the Role:We’re looking for an Associate Director, Clinical Trial Operation on the Clinical Operations team to help us expand what’s possible for patients with serious diseases....Full timeContract workLocal areaRemote workFlexible hours- ...commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market... ...help shape the future of MedTech. Position Overview The Associate Director, Digital Health Studies provides senior leadership for the...Full timeWork at officeRemote work
$146.3k - $234.1k
...At BioNTech, we are committed to revolutionizing medicine through cutting-edge science and innovation. As Associate Director, Clinical Pharmacology & Pharmacometrics, you will play a pivotal role in advancing our drug development pipeline. With limited supervision...Hourly payWorldwide$120k - $156k
...Xyzagen (ZiZaGen) is seeking a highly skilled scientist with a background in Pharmaceutical Sciences to be Associate Director of Clinical Pharmacology. This role is designed for a professional who will lead the design, execution, and interpretation of clinical pharmacology...Full timeContract workWork at officeLocal areaRemote workWorldwideVisa sponsorshipWork visa$143.3k - $193.3k
...is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Regional Clinical Study Management based in the United States. This is a strategic clinical operations leadership role overseeing...Full timeWork at officeLocal areaRemote workFlexible hours$142.5k - $256.5k
...leader, you will define and execute phase-appropriate stability strategies across a diverse mRNA portfolio spanning development, clinical, and commercial products.You will operate as a cross-functional subject matter expert, translating complex stability data into actionable...Permanent employmentFull timeWork at officeWork from homeWorldwide$136.6k - $257.4k
Job Description SummaryAs the Associate Director, Clinical Supply Management, you will lead, represent, manage, and support US Medical Affairs CSM team by developing drug supply strategy and tactical approach for Sponsored, Investigator Initiated (IITs), Managed Access...Full timeWork experience placementLocal areaRemote workRelocation$95 - $120 per hour
...Overview Associate Director, Clinical Scientist – Contract — Boston, REMOTE USA Proclinical is seeking an Associate Director, Clinical Scientist to join a fast-paced Immunology Clinical Research team on a contract basis. This remote role is based in the USA, and...Hourly payContract workRemote work$183.8k - $294.1k
...year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Job Description The Associate Director, Clinical Affairs reports to the Senior Director, Medical Affairs and leads Clinical Affairs operations globally for the Waters...Hourly payContract workWork at officeRemote workWorldwideShift work- Role: Senior scientist specializing in clinical pharmacology and pharmacometrics to advance Bausch + Lomb's ophthalmic pipeline, including dry eye, glaucoma, and retinal disease. Responsibilities lead PK, PD, ADME, modeling, and nonclinical studies develop strategies for...Remote work
- Elevance Health seeks a Clinical Operations Associate Medical Director to support medical management staff in delivering timely, consistent medical decisions for members and providers. The role requires MD/DO with board certification and active license, with Family/Internal...Remote work
- ...Character Biosciences is seeking an experienced Associate Director, Data Management to build and lead the Data Management function for the Dry AMD program. Remote work within the United States is available as the company scales data operations from the ground up. You...Remote work
- ...Job Summary: The Associate Director provides leadership role in facilitating the management of the multiple Phase I-IV clinical research trials across all geographic and functional areas; Responsible for ensuring that direct reports and assigned clinical operation's team...Contract workWork experience placementWork from home
- ...spirit that truly encourages diversity and a powerful “can-do” attitude. #WeChangeDentistry every day. Be part of it. The Associate Director, Clinical Market Development & Professional Relations reports to the Sr Director of NAM Medical Education and is responsible for...Full timeWork at officeRemote work
- ...Position Title: Associate Director, Program Management – Clinical, Medical & Regulatory Location: Remote/Philadelphia, PA Reports to: Sr. Director, Program Management Department: Program Management Office Cabaletta Bio (Nasdaq: CABA) is a late-stage clinical...Remote work
$174.7k - $210.4k
...Associate Director, Product Management, Oncology Clinical Trial Matching US Remote Position Summary: The Associate Director of Product Management, Oncology, leads the development and commercialization of Signatera clinical trial matching products and services for...Remote jobWork at officeImmediate startWorldwide- ...Natera seeks an Associate Director of Product Management to lead development and commercialization of Signatera clinical trial matching products in oncology. The role involves strategic roadmap planning, cross-functional leadership, and driving product performance to...
- ...Piper Companies is seeking an Associate Director of Clinical Operations to lead end-to-end clinical trial management for a CRO, based in Bethesda, MD with remote work options. The role requires 10+ years in pharma/CRO, strong leadership, regulatory knowledge (FDA/GCP...Remote job
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director, Clinical Pathologist. Be the first to apply!
- associate director contracts Remote
- associate manager brand marketing Remote
- remote associate product manager Remote
- associate manager Remote
- associate account manager Remote
- associate medical director Remote
- associate business manager Remote
- associate director Remote
- associate marketing manager Remote
- associate director clinical research Remote





