Bristol Myers Squibb
Medical Director, Radiopharmaceutical Imaging (RPI)
Bristol Myers Squibb, San Diego, California, United States, 92189
Medical Director, Radiopharmaceutical Imaging (RPI)
Position: Medical Director, Radiopharmaceutical Imaging (RPI)
Location: San Diego, CA (Remote options available)
Compensation: $265,740 - $322,014 (US) or $286,999 - $347,775 (San Diego)
Job Responsibilities
Interact with clinical investigators and thought leaders to design a diagnostic imaging strategic plan.
Lead internal project teams, partner with investigators and CROs to design and implement clinical studies of radiopharmaceutical imaging agents.
Contribute to writing of protocols, investigator brochures, clinical study reports, and review other clinical trial and regulatory documents.
Conduct investigator meetings and lead site qualification and initiation visits with clinical trial investigators.
Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets.
Translate findings from research and nonclinical studies into diagnostic imaging development opportunities.
Oversee Data Review and Independent Data Monitoring Committees as applicable.
Conduct clinical trials using ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with external guidelines.
Establish and maintain positive relationships with clinical trial investigators and thought leaders.
Serve as clinical lead for regulatory interactions, including preparation of briefing documents and attendance and presentation at health authority meetings.
Work closely with commercial and medical affairs organization to develop and execute on a diagnostic imaging program for RayzeBio portfolio.
Travel approximately 30% of the time; evening and weekend work may be required.
Education and Experience
MD or equivalent with at least 5 years of pharmaceutical, biotech, or academic clinical experience in oncology diagnostic development, or 3 years for candidates with a track record of developing radiopharmaceutical imaging agents through a regulatory process.
Skills and Qualifications
Patient-focused, deep commitment to understanding needs and improving the lives of patients with cancers.
Motivated to work in a fast-paced, high accountability environment.
Demonstrated record of accomplishment in a compressed time frame.
Experience in all aspects of protocol conduct, including writing, start‑up, study execution, analysis, and reporting.
Strong written and oral communication, presentation, and data analysis skills.
Ability to collaborate successfully with multiple functions in team environments.
Knowledge of GCP and ICH guidelines; experience in regulated environments.
Experience working closely with investigative sites, including principal investigators and site personnel.
Solid understanding of radiopharmaceutical imaging agent development and approval processes.
Physical Demands & Work Environment Duty requires sitting, reaching with hands, and occasional lifting up to 20 pounds. Comfortable with moderate noise levels.
Equal Employment Opportunity BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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Location: San Diego, CA (Remote options available)
Compensation: $265,740 - $322,014 (US) or $286,999 - $347,775 (San Diego)
Job Responsibilities
Interact with clinical investigators and thought leaders to design a diagnostic imaging strategic plan.
Lead internal project teams, partner with investigators and CROs to design and implement clinical studies of radiopharmaceutical imaging agents.
Contribute to writing of protocols, investigator brochures, clinical study reports, and review other clinical trial and regulatory documents.
Conduct investigator meetings and lead site qualification and initiation visits with clinical trial investigators.
Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets.
Translate findings from research and nonclinical studies into diagnostic imaging development opportunities.
Oversee Data Review and Independent Data Monitoring Committees as applicable.
Conduct clinical trials using ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with external guidelines.
Establish and maintain positive relationships with clinical trial investigators and thought leaders.
Serve as clinical lead for regulatory interactions, including preparation of briefing documents and attendance and presentation at health authority meetings.
Work closely with commercial and medical affairs organization to develop and execute on a diagnostic imaging program for RayzeBio portfolio.
Travel approximately 30% of the time; evening and weekend work may be required.
Education and Experience
MD or equivalent with at least 5 years of pharmaceutical, biotech, or academic clinical experience in oncology diagnostic development, or 3 years for candidates with a track record of developing radiopharmaceutical imaging agents through a regulatory process.
Skills and Qualifications
Patient-focused, deep commitment to understanding needs and improving the lives of patients with cancers.
Motivated to work in a fast-paced, high accountability environment.
Demonstrated record of accomplishment in a compressed time frame.
Experience in all aspects of protocol conduct, including writing, start‑up, study execution, analysis, and reporting.
Strong written and oral communication, presentation, and data analysis skills.
Ability to collaborate successfully with multiple functions in team environments.
Knowledge of GCP and ICH guidelines; experience in regulated environments.
Experience working closely with investigative sites, including principal investigators and site personnel.
Solid understanding of radiopharmaceutical imaging agent development and approval processes.
Physical Demands & Work Environment Duty requires sitting, reaching with hands, and occasional lifting up to 20 pounds. Comfortable with moderate noise levels.
Equal Employment Opportunity BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
#J-18808-Ljbffr