Senior Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)
Regeneron
June 27, 2026
On-site
Tarrytown, NY
Clinical Research and Development
Role Summary
The Senior Manager, Internal Medicine, Clinical Scientist leads the development, evaluation, planning, and execution of clinical studies and ensures integrity and interpretation of study data within a clinical development program. Leads in a matrix, cross-functional environment and collaborates with Medical Director(s) (MDs) to design and deliver clinical studies and programs.
Responsibilities (typical day)
- Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings; participate in cross-department collaboration as a member of the Clinical Study Team and Global Clinical SubTeam.
- Develop/maintain knowledge of therapeutic disease area(s), drug candidate (disease biology, clinical manifestations, standard practice), and drug landscape/mechanism of action.
- Support initiation and execution of early and/or late-stage clinical research and development studies; assist with Expanded Synopsis; author and/or review protocol and amendments.
- Assist with and may author/review medical monitoring plans, Statistical Analysis Plans (SAPs), informed consents, and Clinical Study Report clinical components; support regulatory document development; perform quality review.
- Maintain compliance with FDA/EMEA/ICH/GCP and applicable SOPs for clinical safety.
- Perform clinical/medical data review, including safety monitoring to ensure patient safety.
- Collaborate with internal functions and external vendors to promote study integrity.
- Apply analytical skills to connect study objectives/design to data analysis; identify critical risks and mitigations; promote consistent medical/clinical data review techniques.
Qualifications
- BS/MS/PhD/PharmD in a related field.
- ≥ 8 years of pharmaceutical clinical drug development experience.
- Experience in Immune/Inflammatory related clinical trials (one or more therapeutic areas).
Skills/Requirements
- Ability to influence within and across functions; strong analytical, influencing, communication, and presentation skills.
- Strong management, interpersonal, and problem-solving skills.
- Proven knowledge of drug development process, GCP, study design, clinical research methodology, and medical writing; knowledge of regulatory requirements and ICH/GCP; track record of clinical trial process improvements.
Application
- Apply now.
The Senior Manager, Internal Medicine, Clinical Scientist leads the development, evaluation, planning, and execution of clinical studies and ensures integrity and interpretation of study data within a clinical development program. Leads in a matrix, cross-functional environment and collaborates with Medical Director(s) (MDs) to design and deliver clinical studies and programs.
Responsibilities (typical day)
- Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings; participate in cross-department collaboration as a member of the Clinical Study Team and Global Clinical SubTeam.
- Develop/maintain knowledge of therapeutic disease area(s), drug candidate (disease biology, clinical manifestations, standard practice), and drug landscape/mechanism of action.
- Support initiation and execution of early and/or late-stage clinical research and development studies; assist with Expanded Synopsis; author and/or review protocol and amendments.
- Assist with and may author/review medical monitoring plans, Statistical Analysis Plans (SAPs), informed consents, and Clinical Study Report clinical components; support regulatory document development; perform quality review.
- Maintain compliance with FDA/EMEA/ICH/GCP and applicable SOPs for clinical safety.
- Perform clinical/medical data review, including safety monitoring to ensure patient safety.
- Collaborate with internal functions and external vendors to promote study integrity.
- Apply analytical skills to connect study objectives/design to data analysis; identify critical risks and mitigations; promote consistent medical/clinical data review techniques.
Qualifications
- BS/MS/PhD/PharmD in a related field.
- ≥ 8 years of pharmaceutical clinical drug development experience.
- Experience in Immune/Inflammatory related clinical trials (one or more therapeutic areas).
Skills/Requirements
- Ability to influence within and across functions; strong analytical, influencing, communication, and presentation skills.
- Strong management, interpersonal, and problem-solving skills.
- Proven knowledge of drug development process, GCP, study design, clinical research methodology, and medical writing; knowledge of regulatory requirements and ICH/GCP; track record of clinical trial process improvements.
Application
- Apply now.