Remote Senior Oncology Clinical Scientist

Jobgether; United States; Remote; USD 150,000 - 190,000; Full time

Job summary

Jobgether, a partner-driven opportunity, seeks a Senior Clinical Scientist – Oncology for a home-based role in the United States. You will lead oncology studies, contribute to protocol design, and oversee medical monitoring and safety assessments across trial lifecycles.

Collaborate with cross-functional teams and external stakeholders, contribute to regulatory documentation and publications, and mentor junior scientists to ensure high-quality trial delivery and scientific rigor.

Qualifications

• Bachelor's in Life Sciences with ≥7 years' clinical research.
• Master's or PhD with ≥5 years in life sciences.
• Candidates without a Life Sciences degree must have significant clinical development experience, typically exceeding 11 years.
• At least two years of pharmaceutical or clinical drug development experience as a lead Clinical Scientist.
• Strong oncology clinical research experience and solid understanding of oncology trials.

Responsibilities

• Lead or support oncology studies ensuring protocol integrity.
• Serve as primary scientific contact for stakeholders.
• Contribute to trial design and endpoint development.
• Lead medical monitoring and safety assessments.
• Collaborate with medical writers on protocols and docs.
• Prepare CSRs, regulatory submissions, and publications.
• Mentor junior Clinical Scientists.

Skills

Oncology experience

Medical monitoring

Clinical study design

Data analysis

Regulatory documentation

Communication skills

Travel up to 15%

Education

Life Sciences degree (BSc)

Advanced degree (MSc/PhD)

Tools

Microsoft Excel

Microsoft PowerPoint

Job description

Jobgether, a partner-driven opportunity, seeks a Senior Clinical Scientist – Oncology for a home-based role in the United States. You will lead oncology studies, contribute to protocol design, and oversee medical monitoring and safety assessments across trial lifecycles.

Collaborate with cross-functional teams and external stakeholders, contribute to regulatory documentation and publications, and mentor junior scientists to ensure high-quality trial delivery and scientific rigor.