Type: Contract (Initial 3 months with potential extension)
Job Summary:
We are seeking a Senior Clinical Scientist to support late-stage oncology programs within a clinical-stage biopharmaceutical environment. This role will lead clinical development strategy and execution providing scientific oversight across global clinical trials.
The ideal candidate will bring deep expertise in oncology clinical development with strong experience in late-phase studies and cross-functional leadership.
Key Responsibilities
Lead the development and execution of Clinical Development Plans (CDP) including strategy indication prioritization and milestone planning
Provide scientific input into protocol design study endpoints and data analysis plans for Phase III oncology studies
Serve as the scientific lead on cross-functional study teams
Author and review key documents including protocols investigator brochures clinical study reports and regulatory submissions (INDs CTAs)
Partner with Clinical Operations to support study execution data review and issue resolution
Collaborate with Biostatistics on statistical analysis plans and endpoint development
Engage with Key Opinion Leaders (KOLs) and support investigator meetings and external collaborations
Represent Clinical Science in governance and cross-functional discussions
Required Qualifications
Ph.D. or PharmD with 10 years of industry experience
Strong background in oncology clinical development
Experience leading or contributing to global Phase III clinical trials
Deep understanding of oncology biology translational science and PK/PD
Proven experience developing and executing Clinical Development Plans
Excellent scientific writing data interpretation and communication skills
Job Title: Senior Clinical Scientist Oncology Location: Remote (PST working hours preferred) Type: Contract (Initial 3 months with potential extension) Job Summary: We are seeking a Senior Clinical Scientist to support late-stage oncology programs within a clinical-stage biopharmaceutical env...
Job Title: Senior Clinical Scientist Oncology
Location: Remote (PST working hours preferred)
Type: Contract (Initial 3 months with potential extension)
Job Summary:
We are seeking a Senior Clinical Scientist to support late-stage oncology programs within a clinical-stage biopharmaceutical environment. This role will lead clinical development strategy and execution providing scientific oversight across global clinical trials.
The ideal candidate will bring deep expertise in oncology clinical development with strong experience in late-phase studies and cross-functional leadership.
Key Responsibilities
Lead the development and execution of Clinical Development Plans (CDP) including strategy indication prioritization and milestone planning
Provide scientific input into protocol design study endpoints and data analysis plans for Phase III oncology studies
Serve as the scientific lead on cross-functional study teams
Author and review key documents including protocols investigator brochures clinical study reports and regulatory submissions (INDs CTAs)
Partner with Clinical Operations to support study execution data review and issue resolution
Collaborate with Biostatistics on statistical analysis plans and endpoint development
Engage with Key Opinion Leaders (KOLs) and support investigator meetings and external collaborations
Represent Clinical Science in governance and cross-functional discussions
Required Qualifications
Ph.D. or PharmD with 10 years of industry experience
Strong background in oncology clinical development
Experience leading or contributing to global Phase III clinical trials
Deep understanding of oncology biology translational science and PK/PD
Proven experience developing and executing Clinical Development Plans
Excellent scientific writing data interpretation and communication skills