Director / Sr Director, Clinical Science (Oncology, Contract)
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This range is provided by Investigo. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$180.00/hr - $200.00/hr
Direct message the job poster from Investigo
Talent Consultant | Focused on Quality & Compliance
We are supporting a confidential, public, clinical-stage biotechnology company focused on precision oncology . The organization is advancing multiple targeted oncology programs and is seeking an experienced Clinical Science leader to support ongoing and upcoming clinical studies.
This role partners closely with senior oncology development leadership and serves as the medical-scientific voice on one or more clinical programs. The position is hands‑on , execution‑focused, and ideal for someone who enjoys being deeply embedded in study design, data interpretation, and cross‑functional collaboration.
Key Responsibilities
- Partner with clinical leadership to develop clinical development concepts and plans , with emphasis on early oncology programs
- Lead or contribute to protocol synopses, protocols, and amendments
- Author and review informed consent forms (ICFs) and adjudicate site‑specific ICF requests
- Collaborate with Clinical Operations on site selection, start‑up, and ongoing site communication
- Write and maintain Investigator Brochures , including annual updates
- Contribute to or author clinical and safety sections of regulatory submissions (e.g., NDA/MAA)
- Represent Clinical Science on cross‑functional study teams
- Review and interpret clinical data listings , including safety and SAE data
- Author or support Clinical Study Reports (CSRs) and related publications
- Develop study‑ and program‑level presentations and slide decks
- Train internal teams, CROs, and site staff on protocols and therapeutic area
- Support Health Authority interactions , including responses to inspections and audits
- Assist with or serve as Medical Monitor for Phase 2 or Phase 3 clinical trials
Qualifications
- Bachelor’s degree required with strong clinical oncology knowledge
- Advanced degree preferred (MD, PharmD, PhD, NP, or Master’s in a relevant field)
- 4+ years of industry oncology clinical development experience
- Demonstrated involvement across the full clinical trial lifecycle (start‑up through CSR)
- Experience with small‑molecule oncology trials strongly preferred
- Strong skills in protocol design, data interpretation, and safety oversight
- Working knowledge of Good Clinical Practice (GCP)
- Excellent written and verbal communication skills
- Ability to thrive in a fast‑paced, evolving biotech environment
Candidates from closely related disciplines (e.g., Clinical Operations, Regulatory Affairs, Biometrics) who have represented their function on study teams may also be considered.
Additional Information
- On‑site presence is required (San Diego or South San Francisco)
- This is a 18‑month contract position with high visibility and impact