Agile 1 - Regeneron
Temporary - Associate Director, Clinical Scientist, Hematology
Skills
2 months ago
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Important information
Contract type:
Permanent, Freelance / Contract
Salary:
$218,400 – $270,400 / year
Location:
United States
Work mode:
Remote
Published on:
13 August 2026
What they need
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, atopic dermatitis, asthma, COPD, chronic rhinosinusitis with nasal polyps (CRSwNP), eosinophilic esophagitis (EoE), oncology, hypercholesterolemia, and rare inflammatory conditions. Regeneron also has product candidates in development in other areas of high unmet medical need.
Temporary Associate Director Clinical Scientist Hematology - R48455
Position Description
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Temporary Associate Director, Clinical Sciences to join our Hematology Clinical Sciences team, supporting our clinical development organization in a Remote role. In this role, you will help design, execute, and ensure the scientific integrity of hematology clinical studies while collaborating with Medical Directors and cross-functional program teams to advance early- and late-stage clinical development programs. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
Roles Responsibilities
- Serve as Clinical Scientist for the program, or as delegate to the Therapeutic Area Clinical Scientist
- Contribute to program team meetings, scientific advisory boards, steering committees, and data/safety monitoring meetings
- Maintain deep understanding of disease biology, clinical manifestations, and the compound's mechanism of action
- Design and execute clinical research studies for early- and late-stage assets, grounded in supporting literature
- Author the Expanded Synopsis and clinically relevant protocol sections, medical monitoring plans, and SAPs
- Prepare and present information for external stakeholder meetings, investigator meetings, and internal collaborators
- Apply analytical expertise to assess how program design impacts data analysis, and identify risk mitigation strategies
- Promote consistent clinical data review conventions and author medical monitoring plans across studies
Skills
- Bachelor's degree required; advanced degree (PhD/PharmD/MSc) in life science or healthcare preferred
- 10+ years of pharmaceutical clinical drug development experience, with working knowledge of oncology or hematology therapeutic areas
- Relate confidently and diplomatically with people at every level, internally and externally
- Influence effectively within your team and across functional
- Manage cross-functional relationships with strong interpersonal skills
- Pay close attention to detail across complex, matrixed programs
- Thrive as a collaborative, team-oriented contributor
- Communicate clinical strategy clearly to both scientific and non-scientific audiences
- Strong understanding of drug development processes, Good Clinical Practice, and clinical research methodology
- Solid medical writing skills and experience across global clinical trial execution
This is a contract position at Regeneron in partnership with Agileone and Allsource as the Employer of Record.
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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
Pay: $105.00 - $130.00 per hour
Work Location: Remote
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