Working with Us

　　Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

　　Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

　　Functional Area Description

　　The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.

　　Position Summary / Objective

　　Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct

　　May serve as Clinical Trial Lead for one or more trials

　　May lead or support trial level activities for one or more trials with the necessary supervision

　　May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members

　　Position Responsibilities

　　Collaborate and liaise with external partners (e.g., KOLs)

　　Seek out and enact best practices with instruction

　　Provide regular and timely updates to manager/management as requested

　　Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required

　　Conduct literature review

　　Submit clinical documents to TMF

　　Develop site and CRA training materials and present these at SIVs and Investigator meetings

　　Review clinical narratives

　　Monitor clinical data for specific trends

　　Develop Data Review Plan in collaboration with Data Management

　　Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming

　　Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)

　　Degree Requirements

　　Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred). Appropriate for new entrance to pharma (post fellowship/ new to industry)Experience Requirements

　　Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations

　　Ability to understand assigned protocol(s) and their requirements

　　Basic knowledge skills to support program-specific data review and trend identification

　　Intermediate medical writing skills and medical terminology

　　Basic planning/project management skills (develop short range plans that are realistic and effective)

　　Key Competency Requirements

　　Detail-oriented with commitment to quality

　　Basic knowledge of disease area, compound, current clinical landscape

　　Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees

　　Intermediate critical thinking and problem-solving skills

　　Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)

　　Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools)

　　Travel Required

　　Domestic and International travel may be required.

　　The starting compensation for this job is a range from $121,000-$172,000, plus incentive cash and stock opportunities (based on eligibility).

　　The starting pay rate takes into account characteristics of the job, such as required skills and the where the job is performed.

　　Final individual compensation will be decided based on demonstrated experience.

　　For more on benefits, please visit our https://careers.bms.com/working-with-us.

　　Eligibility for specific benefits listed on our BMS Careers site may vary based on the job and location.

　　If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

　　Uniquely Interesting Work, Life-changing Careers

　　With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

　　On-site Protocol

　　Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

　　BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected] . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.

　　BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

　　BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

　　Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

　　Company: Bristol Myers Squibb

　　Req Number: R1576168

　　Updated: 2023-11-30 21:04:52.558 UTC

　　Location: Princeton,New Jersey

　　Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.