Senior Director, Clinical Science (Contractor) - Oncology
Location:
South San Francisco, CA or San Diego, CA
Contract:
18-month contractor assignment
Pay Rate:
High $150-170/hr (range dependent on experience)
Our client is a precision medicine oncology company building targeted therapies for molecularly defined solid tumors. This is a contractor role supporting clinical development activities with an emphasis on early oncology development, partnering closely with a clinical leader and cross-functional teams.
What you’ll do
Support clinical development concepts and plans (early oncology focus, cross-stage exposure)
Draft and review protocol synopses, protocols, and amendments
Write/review ICFs and manage site-specific ICF review requests
Partner with Clinical Operations on site selection, start-up, and site communication
Lead clinical content for Investigator’s Brochures (initial and annual updates)
Review safety data, listings, and SAEs; support patient safety oversight with the clinical lead
Contribute to CSRs, publications, slide decks, and clinical/safety sections for regulatory submissions
What we’re looking for
BS/BA plus strong clinical oncology knowledge from clinical development experience
4+ years industry oncology experience
Clinical trial lifecycle experience (start-up through CSR preferred)
Protocol design, data interpretation, and safety/AE assessment experience
Strong knowledge ofCP
High-quality scientific writing and clear cross-functional communication
Comfortable in a fast-paced environment
Note: This is a role supporting one of our clients and is not a position at GQR.
#J-18808-Ljbffr
Location:
South San Francisco, CA or San Diego, CA
Contract:
18-month contractor assignment
Pay Rate:
High $150-170/hr (range dependent on experience)
Our client is a precision medicine oncology company building targeted therapies for molecularly defined solid tumors. This is a contractor role supporting clinical development activities with an emphasis on early oncology development, partnering closely with a clinical leader and cross-functional teams.
What you’ll do
Support clinical development concepts and plans (early oncology focus, cross-stage exposure)
Draft and review protocol synopses, protocols, and amendments
Write/review ICFs and manage site-specific ICF review requests
Partner with Clinical Operations on site selection, start-up, and site communication
Lead clinical content for Investigator’s Brochures (initial and annual updates)
Review safety data, listings, and SAEs; support patient safety oversight with the clinical lead
Contribute to CSRs, publications, slide decks, and clinical/safety sections for regulatory submissions
What we’re looking for
BS/BA plus strong clinical oncology knowledge from clinical development experience
4+ years industry oncology experience
Clinical trial lifecycle experience (start-up through CSR preferred)
Protocol design, data interpretation, and safety/AE assessment experience
Strong knowledge ofCP
High-quality scientific writing and clear cross-functional communication
Comfortable in a fast-paced environment
Note: This is a role supporting one of our clients and is not a position at GQR.
#J-18808-Ljbffr