Bristol Myers Squibb
Associate Director, Clinical Science
Bristol Myers Squibb, San Diego, California, United States, 92189
Associate Director, Clinical Science – Bristol Myers Squibb
Working with Us Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb is anything but ordinary. Here, uniquely interesting work happens every day in every department—from optimizing a production line to advancing breakthroughs in cell therapy. The work transforms patients’ lives and the careers of those who do it. You’ll have the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams, and take your career farther than you thought possible.
Summary The Associate Director of Clinical Science plays a supportive role in the clinical development of RazyeBio radiopharmaceuticals for oncology indications. Working in collaboration with clinical development, you will be responsible for various aspects of the ongoing clinical trial program in the relevant therapeutic area—including program implementation, study start‑up/execution/close‑out, data analysis/reporting, and potential support of NDA/MAA filings.
Job Responsibilities
Acquire and utilize knowledge of clinical trial design to develop or oversee specific study concept synopses and protocols.
Participate in protocol review discussions concerning scientific and procedural aspects of study design.
In collaboration with Medical Writing and Clinical Operations, prepare study protocols, amendments, specific sections of study manuals, Investigator meeting materials, and other documents under appropriate guidance and supervision.
Contribute to the design, development, and review of CRFs, Data Management Manuals, and Data Analysis Plans.
Review ongoing clinical data.
Organize and oversee Data Review Committee meetings, including preparation of slides and other review materials.
Under MD supervision, address scientific and procedural questions from investigators.
Assist in the preparation/review of INDs, regulatory documents, IND annual reports/DSURs, Investigator Brochures, and NDAs/MAAs.
Support priorities within the functional area.
Anticipate moderately complex obstacles within a clinical study and, with guidance, implement solutions.
May be asked to coordinate teams and provide direction.
May lead two or more components of departmental strategic initiatives.
Enter a new therapeutic area and summarize published scientific information for new study development.
Maintain strong verbal and written communication skills and interpersonal skills to ensure scientific integrity of clinical studies.
Serve as a subject‑matter expert to advise others within the company on moderate‑complex problems.
Travel approximately 20% of the time.
Education and Experience
PharmD or PhD preferred.
6+ years of relevant drug development experience with a MS.
8+ years of relevant drug development experience with a BS degree in Biological Sciences, health care, or a related field.
Minimum 5 years’ experience in clinical research or clinical pharmacology within a biotech/pharmaceutical company or contract research organization.
Skills and Qualifications
Fast learner with strong adaptability to change.
Proficient with Microsoft Office (Excel, PowerPoint, etc.) and industry programs such as SpotFire.
Knowledge of FDA, EMA and ICH regulations and guidelines.
Ability to collaborate cross‑functionally at all organizational levels.
Compensation Overview Princeton, NJ – $173,217 – $209,899 San Diego, CA – $190,539 – $230,888 Additional incentive cash and stock opportunities may be available. Final pay is determined by demonstrated experience.
Benefits
Health Coverage: Medical, pharmacy, dental, and vision care.
Well‑being Support: BMS Well‑Being Account, BMS Living Life Better, Employee Assistance Programs.
Financial Well‑being and Protection: 401(k) plan, disability insurance, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, survivor support.
Work‑Life Benefits Paid Time Off and flexible scheduling. US Exempt Employees may enjoy unlimited time off with manager approval, 11 paid national holidays (excluding Phoenix, AZ, Puerto Rico, or RayzeBio employees). Phoenix, AZ, Puerto Rico, and RayzeBio employees have 160 hours annual paid vacation, 11 national holidays, and 3 optional holidays. Additional time off may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs. Global Shutdown occurs annually from Christmas to New Year’s Day for all eligible global employees.
Support for People With Disabilities Applicants may request reasonable accommodations before accepting a job offer. Contact adastaffingsupport@bms.com for accommodation requests. Visit careers.bms.com/eeo-accessibility for the full Equal Employment Opportunity statement.
Candidate Rights BMS considers qualified applicants with arrest and conviction records pursuant to applicable laws.
Data Protection BMS will never request payments, financial information, or Social Security numbers during the application process. Learn more at careers.bms.com/fraud-protection.
Requisition: R1597108 – Associate Director, Clinical Science.
#J-18808-Ljbffr
Working with Us Challenging. Meaningful. Life‑changing. Working at Bristol Myers Squibb is anything but ordinary. Here, uniquely interesting work happens every day in every department—from optimizing a production line to advancing breakthroughs in cell therapy. The work transforms patients’ lives and the careers of those who do it. You’ll have the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high‑achieving teams, and take your career farther than you thought possible.
Summary The Associate Director of Clinical Science plays a supportive role in the clinical development of RazyeBio radiopharmaceuticals for oncology indications. Working in collaboration with clinical development, you will be responsible for various aspects of the ongoing clinical trial program in the relevant therapeutic area—including program implementation, study start‑up/execution/close‑out, data analysis/reporting, and potential support of NDA/MAA filings.
Job Responsibilities
Acquire and utilize knowledge of clinical trial design to develop or oversee specific study concept synopses and protocols.
Participate in protocol review discussions concerning scientific and procedural aspects of study design.
In collaboration with Medical Writing and Clinical Operations, prepare study protocols, amendments, specific sections of study manuals, Investigator meeting materials, and other documents under appropriate guidance and supervision.
Contribute to the design, development, and review of CRFs, Data Management Manuals, and Data Analysis Plans.
Review ongoing clinical data.
Organize and oversee Data Review Committee meetings, including preparation of slides and other review materials.
Under MD supervision, address scientific and procedural questions from investigators.
Assist in the preparation/review of INDs, regulatory documents, IND annual reports/DSURs, Investigator Brochures, and NDAs/MAAs.
Support priorities within the functional area.
Anticipate moderately complex obstacles within a clinical study and, with guidance, implement solutions.
May be asked to coordinate teams and provide direction.
May lead two or more components of departmental strategic initiatives.
Enter a new therapeutic area and summarize published scientific information for new study development.
Maintain strong verbal and written communication skills and interpersonal skills to ensure scientific integrity of clinical studies.
Serve as a subject‑matter expert to advise others within the company on moderate‑complex problems.
Travel approximately 20% of the time.
Education and Experience
PharmD or PhD preferred.
6+ years of relevant drug development experience with a MS.
8+ years of relevant drug development experience with a BS degree in Biological Sciences, health care, or a related field.
Minimum 5 years’ experience in clinical research or clinical pharmacology within a biotech/pharmaceutical company or contract research organization.
Skills and Qualifications
Fast learner with strong adaptability to change.
Proficient with Microsoft Office (Excel, PowerPoint, etc.) and industry programs such as SpotFire.
Knowledge of FDA, EMA and ICH regulations and guidelines.
Ability to collaborate cross‑functionally at all organizational levels.
Compensation Overview Princeton, NJ – $173,217 – $209,899 San Diego, CA – $190,539 – $230,888 Additional incentive cash and stock opportunities may be available. Final pay is determined by demonstrated experience.
Benefits
Health Coverage: Medical, pharmacy, dental, and vision care.
Well‑being Support: BMS Well‑Being Account, BMS Living Life Better, Employee Assistance Programs.
Financial Well‑being and Protection: 401(k) plan, disability insurance, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, survivor support.
Work‑Life Benefits Paid Time Off and flexible scheduling. US Exempt Employees may enjoy unlimited time off with manager approval, 11 paid national holidays (excluding Phoenix, AZ, Puerto Rico, or RayzeBio employees). Phoenix, AZ, Puerto Rico, and RayzeBio employees have 160 hours annual paid vacation, 11 national holidays, and 3 optional holidays. Additional time off may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs. Global Shutdown occurs annually from Christmas to New Year’s Day for all eligible global employees.
Support for People With Disabilities Applicants may request reasonable accommodations before accepting a job offer. Contact adastaffingsupport@bms.com for accommodation requests. Visit careers.bms.com/eeo-accessibility for the full Equal Employment Opportunity statement.
Candidate Rights BMS considers qualified applicants with arrest and conviction records pursuant to applicable laws.
Data Protection BMS will never request payments, financial information, or Social Security numbers during the application process. Learn more at careers.bms.com/fraud-protection.
Requisition: R1597108 – Associate Director, Clinical Science.
#J-18808-Ljbffr