Clinical Scientist

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