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 .

　　The Senior Clinical Scientist reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.

　　Position Responsibilities:

　　Maintain a thorough understanding of assigned protocols and protocol requirements; educate supporting team members

　　Plan and lead the implementation all study startup/conduct/close-out activities as applicable

　　Evaluate innovative trial designs (collaboration with Medical Monitor/Clinical Development Lead)

　　Protocol and ICF development process with minimal guidance; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing)

　　Site-facing activities such as training and serving as primary contact for clinical questions

　　Activities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review by supporting CS team

　　Clinical data trend identification; provide trends and escalate questions to Medical Monitor

　　Develop clinical narrative plan; review clinical narratives

　　Provision of information required by Protocol Manager for development of trial budget, CRO scope of work, etc.

　　Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities

　　Drafting/review and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)

　　Collaborate and serve as primary liaison between external partners for scientific advice

　　Degree Requirements:

　　Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)Experience Requirements:

　　Strong experience in clinical science, clinical research, or equivalent

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

　　Proficient knowledge and skills to support program specific data review, trend identification, data interpretation

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

　　Key Competency Requirements:

　　Excellent verbal, written, communication and interpersonal skills

　　Must be able to effectively communicate and collaborate across functions and job levels

　　Ability to assimilate technical information quickly

　　Routinely takes initiative

　　Detail-oriented

　　Strong sense of teamwork; ability to lead team activities

　　Proficient in Medical Terminology and medical writing skills

　　Proficient knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile)

　　Proficient critical thinking, problem solving, decision making skills

　　Understanding of functional and cross-functional relationships

　　Commitment to Quality

　　Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism

　　Proficient planning/project management skills (ability to develop short to mid-range plans that are realistic and effective in meeting goals)

　　Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting tools

　　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: R1577835

　　Updated: 2024-01-22 14:03:48.574 UTC

　　Location: Summit,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.