Senior Oncology Clinical Development Director

Physician Pivot; Alameda (CA); On-site; USD 318,000 - 402,000; Full time

Benefits offered by this job

401k plan

Medical, dental and vision coverage

Stock purchase program

Generous paid time off

Job summary

Exelixis, headquartered in Alameda, CA, seeks a senior clinician to lead and execute oncology trials across early and late stages. You will design protocols, monitor safety, interact with investigators, and collaborate with cross-functional teams to advance development.

The role requires MD with oncology/hematology focus and at least 8 years post-residency. You will report safety data, interpret trial results for regulatory agencies, and contribute to scientific strategies for oncology programs.

Qualifications

• MD with oncology/hematology focus required, 8+ years post-residency.
• Equivalent combination of education and experience.
• Experience in biotech or pharma drug development preferred.

Responsibilities

• Design, prepare and initiate study protocols in compliance with GCP.
• Act as medical monitor for company sponsored trials.
• Support project teams with therapeutic area specifics.
• Collaborate with safety group to analyze and report safety data.
• Interpret trial data and prepare regulatory reports.
• Interact with key opinion leaders and investigators.
• Ensure alignment of scientific development strategies for oncology.
• Maintain cutting-edge knowledge in oncology.

Skills

Clinical trial leadership

Medical monitoring

Cross-functional collaboration

Safety data analysis

Regulatory reporting

KOL engagement

Scientific writing

Time management

Education

MD (board certification or eligibility in Oncology or Hematology/Oncology desirable but not essential)

Job description

Exelixis, headquartered in Alameda, CA, seeks a senior clinician to lead and execute oncology trials across early and late stages. You will design protocols, monitor safety, interact with investigators, and collaborate with cross-functional teams to advance development.

The role requires MD with oncology/hematology focus and at least 8 years post-residency. You will report safety data, interpret trial results for regulatory agencies, and contribute to scientific strategies for oncology programs.