A precision?medicine oncology company is seeking an experienced Clinical Scientist to support clinical strategy, protocol development, and execution across early and late?stage oncology programs. This role partners closely with clinical leadership and cross?functional teams to advance targeted therapies for solid tumors.

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.

Qualifications

• Bachelor’s degree required; advanced degree (MS, MD, NP, PharmD, 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.