Oncology Clinical Scientist - Trials & Regulatory Lead

Perspective Therapeutics; United States; On-site; USD 85,000 - 115,000; Full time

Job summary

A biotechnology firm in Waltham, MA, is seeking a Clinical Scientist - Oncology, responsible for developing and overseeing clinical studies in oncology. This role involves collaborating with KOLs, drafting clinical protocols, and ensuring compliance with regulatory standards. Ideal candidates will possess an advanced degree and significant clinical research experience, particularly in oncology and related fields. Generous benefits and a commitment to professional development are offered.

Qualifications

• 3+ years of clinical research experience in biotech or pharmaceutical.
• Hands-on experience with clinical trial design and regulatory submissions.
• Experience developing training materials for clinical sites.

Responsibilities

• Serve as a key scientific liaison with KOLs and investigators.
• Lead the design and review of clinical protocols and ICFs.
• Provide updates on study progress and emerging data trends.

Skills

Strong understanding of GCP, ICH guidelines

Exceptional verbal and written communication skills

Strong leadership skills

Advanced proficiency in medical writing

Education

Advanced or clinical degree (RN, BSN, MSN, MS, PhD, PharmD, MD)

Job description

A biotechnology firm in Waltham, MA, is seeking a Clinical Scientist - Oncology, responsible for developing and overseeing clinical studies in oncology. This role involves collaborating with KOLs, drafting clinical protocols, and ensuring compliance with regulatory standards. Ideal candidates will possess an advanced degree and significant clinical research experience, particularly in oncology and related fields. Generous benefits and a commitment to professional development are offered.