Clinical Trials Director

About Bristol Myers SquibbBristol Myers Squibb is a global leader in the pharmaceutical industry, dedicated to developing innovative treatments and therapies for patients around the world. Our company has a rich history of pioneering new medical breakthroughs and advancing the boundaries of human knowledge.Our TeamOur team of experts is passionate about...

Role OverviewBristol Myers Squibb is an integrated global hub focused on helping patients overcome serious diseases by developing sustainable and innovative solutions. Our technology and drug development activities aim to usher in the next wave of innovation.The Clinical Trial Specialist role has task-level responsibility for document and CTA package...

Job DescriptionWe are seeking a skilled Clinical Trials Specialist to join our team at Bristol Myers Squibb. This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials.Key Responsibilities:Managing and executing on centralized...

About the OpportunityThis is an exciting opportunity to join our Bristol Myers Squibb team as a Director of Clinical Operations. The successful candidate will lead the ECD Clinical Science team in planning and executing clinical trial activities.ResponsibilitiesResponsible for design and execution of assigned clinical trial activities.Collaborate...

About UsBristol Myers Squibb is a global pharmaceutical leader committed to improving patient outcomes through innovation and dedication. We foster a culture of collaboration, creativity, and excellence, driving us to push boundaries and achieve extraordinary results.Job SummaryThis role supports the Patient Engagement & Recruitment (PER) Team in developing...

**Job Summary:**This role is responsible for managing and executing centralized activities in support of global clinical trials with an emphasis on clinical documentation.The ideal candidate will have a strong understanding of clinical trial regulations, including ICH/GCP, and experience in preparing, reviewing, and submitting regulatory documentation to...

About the RoleThe successful candidate will oversee all operational aspects of clinical trials end-to-end, including planning, execution, and interpretation of clinical trial research data collection activities and clinical operations.This includes complete oversight of resource allocation within assigned trials, driving operational excellence through...

Job SummaryThe Imaging Clinical Trial Manager is responsible for coordinating clinical trial activities, including site evaluations, training, and audit preparation. This role requires strong organizational and communication skills, as well as experience in the medical or clinical trials industry.Key Responsibilities:Evaluate sites for capability to...

About the RoleAs a Clinical Trials Project Coordinator at Imaging Endpoints, you will play a vital role in coordinating clinical project activities for our global team. Your primary responsibility will be to work with Operations staff, Sponsor staff, and study sites to ensure seamless execution of clinical trials.Key Responsibilities- Evaluate sites for...

Job Overview">We are seeking an experienced Content Editor to join our Clinical Studies team in Chennai. As a key member of the team, you will be responsible for managing and updating clinical trials information from various sources.">About You">To excel in this role, you should have a strong educational background in Pharmacy or Biotechnology, with a keen...

Job DescriptionAs a Clinical Trial Documentation Lead, you will be responsible for managing a team that reconciles and prepares clinical trial submission documents in accordance with regulatory guidelines. You will ensure consistency across all BMS programs by supervising a team of Clinical Trial Support Specialists and providing support to in-house and...

SUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind....

SUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind....

SUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind....

SUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind....

The Senior Associate, Clinical Trial Submission Management, will help ensure the technical compliance of our Clinical Trial submissions via the smooth compliant flow of information between all functional areas, internal and external to GRAAS, local offices, external partners and regulatory authorities. This vital role is assigned to one or more Amgen...

Key Performance Indicators:The successful candidate will be responsible for achieving the following key performance indicators:Preparation and release of RFI, RFP, and RFQs on time and within budget.Negotiation of contracts that meet commercial and quality standards.Implementation of contract frameworks that meet the needs of both parties.Closure of...

Job Title: Senior Associate, Clinical Trial Submission Management Job Location: Hyderabad, Telangana, India Job Location Type: On-site Job Contract Type: Full-time Job Seniority Level: The Senior Associate, Clinical Trial Submission Management, will help ensure the technical compliance of our Clinical Trial submissions via the smooth compliant flow of...

Job DescriptionWorking with UsChallenging. Meaningful. Life-changing. Those aren&apost 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...

Required Skills and QualificationsTo be successful in this role, you will require:Exceptional working knowledge of clinical trials and the data management role.Excellent organizational and project management skills.Expert knowledge and understanding of ICH Guidelines for Good Clinical Practice and Title 21 of the Code of Federal Regulations.Technical skills...