Senior Clinical Research Scientist - Multiple Myeloma
Bristol Myers Squibb
Boudry, CH
vor 2 Tg.
source : DirectEmployers Association

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. As we continue to progress our clinical research into areas of unmet medical need, we are seeking a Senior Clinical Research Scientist to focus on our trials in Multiple Myeloma.

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 will be responsible for : + Implementation, planning, and execution of assigned clinical trial activities.

  • Serves as Clinical Trial Lead for one or more trials + Successfully leading, plans, and executes 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 collaborate 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 + Clinical data trend identification; provide trends and escalate questions to Medical Monitor + Developing clinical narrative plan;
  • review clinical narratives + Provision 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 + Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees + Excellent verbal, written, communication and interpersonal skills in English + Must be able to effectively communicate and collaborate across functions and job levels + 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 + 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 : R1522881 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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