Protocol Specialist
Bristol-Myers Squibb
Boudry, Switzerland
vor 3 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.Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease.

Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support.

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 the resources to pursue their goals, both at work and in their personal lives.

Responsibilities : This role will be responsible to support the GCO, NRDG book of work with respect to the all operational transactional activities.

Work in global contracting, funds and paymentsTrial Document ManagementWork in Investigator Sponsored (ISR) concept submissions and Request for ProposalGenerate / develop necessary metrics reportsManages and prioritizes other activities as requested by the team (e.

g., create documents / tools for team collaboration, planning meetings, mass mailings, postings on SharePoint etc.) related to Global Clinical Operations (GCO) managed research.

Is able to evaluate which tasks to delegate to Global Clinical Operations (GCO) Administrative staff.Qualifications :

  • Bachelor’s degree required. Degree in nursing, life science or healthcare related field is preferred.
  • 1-3 years’ experience in Clinical Research or related work experience
  • Knowledge of ICH / GCP Guidelines and local regulatory guidelines or regulations is preferred
  • Experience in the use of industry Clinical Trial Management Systems, Clinical Trial Master File Systems and Data Management Systems is preferredAround 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.

    Job InfoType : Full timeLocation : Celgene - Boudry

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