Senior Clinical Scientist Haematology
Bristol-Myers Squibb
Boudry, Switzerland
vor 6 Tg.
source : Experteer

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 activitiesServing as Clinical Trial Lead for one or more trialsSuccessfully leading, plans, and executing trial level activities for multiple trials with minimal to moderate level of supervisionProviding 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 membersMay 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 membersPlanning and leading the implementation all study startup / conduct / close-out activities as applicableEvaluating 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 questionsActivities related to data generation and validation, including CRF design, clinical data review / query resolution;
  • ensure consistent, quality data review by supporting CS teamDeveloping clinical narrative plan; reviewing clinical narrativesProvisioning 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) activitiesDrafting / 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 adviceYour 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 equivalentProficient knowledge of GCP / ICH, drug development process, study design, statistics, clinical operationsProficient knowledge and skills to support program specific data review, trend identification, data interpretationSuccessful experience in writing ProtocolsKnowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committeesExcellent verbal, written, communication in EnglishMust be able to effectively communicate and collaborate across functions and job levelsStrong sense of teamwork;
  • ability to lead team activitiesProficient 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 professionalismProficient 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 toolsAround 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.Full time

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