Clinical Scientist – Hematology
Associate Director / Director Level
Remote (U.S. based, Eastern or Central Time preferred)
Overview
We are partnering with a growing, oncology‑focused biopharmaceutical organization to support the hiring of an experienced Clinical Scientist with a strong background in hematologic malignancies. This role plays a critical part in the design, execution, and scientific oversight of clinical trials across early‑ and late‑stage development, including both investigational and marketed assets.
This is a highly visible, hands‑on role for a Clinical Scientist who thrives in fast‑paced, collaborative environments and is comfortable operating within a matrixed development organization.
Key Responsibilities
- Serve as Clinical Scientist for assigned study protocols and/or programs, supporting study design, execution, and scientific integrity
- Collaborate closely with Medical Directors and cross‑functional teams including Clinical Operations, Data Management, Biostatistics, Regulatory, and Safety
- Contribute to or lead protocol development, amendments, and supporting scientific documentation
- Perform ongoing clinical data review and support patient safety monitoring activities
- Author or review medical monitoring plans, data review plans, and clinical narratives
- Support preparation and review of clinical study reports (CSRs) and clinical sections of regulatory documents (e.g. INDs, IBs, DSURs, PSURs)
- Present clinical data internally and externally, including investigator meetings, advisory boards, and governance forums
- Support site and CRA training materials and participate in Study Initiation Visits (SIVs) as needed
- Partner with external experts and key opinion leaders as appropriate
- Conduct literature reviews to inform development strategy and clinical decision‑making
- Ensure high‑quality clinical documentation and timely responses to protocol or site inquiries
Required Qualifications
- Advanced scientific degree (PhD, PharmD, MD, or MS with significant relevant experience)
- Minimum of 5+ years of experience as a Clinical Scientist or equivalent role within clinical development
- Direct experience in hematologic malignancies is required
- Solid understanding of the drug development process across early and/or late‑stage clinical trials
- Experience working in cross‑functional, matrixed teams
- Strong analytical, problem‑solving, and critical‑thinking skills
- Ability to manage multiple priorities in a dynamic, fast‑moving environment
- Excellent written and verbal communication skills
Preferred Experience
- Experience supporting both investigational and marketed products
- Comfort contributing to regulatory interactions and submissions
- Prior experience in small to mid‑sized biotech or similarly agile environments
- Exposure to global clinical development programs
Work Environment and Logistics
- Remote, U.S.‑based position
- Eastern or Central Time zone strongly preferred due to collaboration with global teams
- Occasional domestic or international travel (approximately 10–20%)
Why This Role
- Opportunity to make a significant scientific impact in hematologic malignancies
- Broad exposure across clinical development lifecycle
- High level of collaboration with experienced clinical and medical leadership
- Competitive compensation aligned to experience and market
