Senior Clinical Scientist Haematology

Profile

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

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

In this role, you are responsible for:


The implementation, planning, and execution of assigned clinical trial activities
Serving as Clinical Trial Lead for one or more trials
Successfully leading, plans, and executing trial level activities for multiple trials with minimal to moderate level of supervision
Providing scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership)
Co-Leading study team meetings in partnership with GDO protocol manager; and collaborating with cross functional study team members
May support clinical development planning (collaboration with Clinical Development Lead/Clinical Trial Physician for provision and analysis of data to support future planning)
Maintaining a thorough understanding of assigned protocols and protocol requirements; educate supporting team members
Planning and leading the implementation all study startup/conduct/close-out activities as applicable
Evaluating 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
Developing clinical narrative plan; reviewing clinical narratives
Provisioning of information required by Protocol Manager for development of trial budget, CRO scope of work, etc.
Reviewing development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities
Drafting/reviewing and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)
Collaborating and serving as primary liaison between external partners for scientific advice


Your Profile:


Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)
5 years of 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
Successful experience in writing Protocols
Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees
Excellent verbal, written, communication in English
Must be able to effectively communicate and collaborate across functions and job levels
Strong sense of teamwork; ability to lead team activities
Proficient knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile)
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


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Company: Bristol-Myers Squibb

Req Number: R1525269_EN

Updated: 2020-06-17 00:00:00.000 UTC

Location: Boudry,Switzerland

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.

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