Director/Senior Director, Clinical Science
Job in
Cary, Wake County, North Carolina, 27518, USA
Listed on 2026-06-07
Listing for:
GQR
Full Time
position Listed on 2026-06-07
Job specializations:
-
IT/Tech
Job Description & How to Apply Below
Key Responsibilities
- Contribute to clinical development plans and protocol design for oncology programs.
- Draft protocol synopses, protocols, amendments, and informed consent forms.
- Support site selection, study start?up, and ongoing clinical operations.
- Lead or contribute to investigator brochures, clinical study reports, and regulatory documents.
- Review and interpret clinical and safety data, including SAEs.
- Prepare scientific and clinical presentations for internal and external audiences.
- Train internal teams, CROs, and study sites on therapeutic areas and protocols.
- Support advisory boards, competitive landscape assessments, and KOL engagement.
- Participate in Health Authority interactions and responses.
- Assist medical monitoring for Phase 2/3 trials, ensuring patient safety and study integrity.
- Bachelor's degree required; advanced degree (MS, MD, NP, Pharm
D, PhD) preferred. - Minimum 4 years of oncology industry experience.
- Experience across clinical trial phases, ideally including small?molecule programs.
- Strong skills in protocol development, data interpretation, and medical monitoring.
- Knowledge of GCP and clinical safety assessment.
- Excellent communication skills and ability to thrive in a fast?paced environment.
Position Requirements
10+ Years
work experience
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