Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.
As we continue to progress our early-stage pipeline, we are seeking a Senior Clinical Research Scientist to join our Research & Early Development (R&ED) group.
We are seeking an individual to lead the clinical science aspects of early development within clinical trials related to hematology, oncology and/or cellular therapy. As Clinical Research Scientist, you will provide the scientific expertise and partnership to the medical lead and cross-functional teams as to work towards developing / executing early development clinical studies.
In a diverse and multi-faceted role, you will oversee the authoring of study protocol/amendments and other clinical trial documentation (e.g. IND/CTA, informed consent forms, study reports), whilst also completing clinical data review, presentation/publication of results and clinical trial site interactions.
Please note: This role is 100% based at our Early Research site in Sevilla, southern Spain - any interested applicants must be willing to live / reside in Sevilla.
Responsibilities - Your day-to-day will encompass:
Provide the scientific expertise necessary to develop and execute early development clinical studies in hematology and oncology indications
Represent Early Clinical Development in cross-functional teams/meetings both internally and externally
Contribute to the authorship/review and amendment of clinical study protocols, consent forms, case report forms, publications and other clinical study documents (IND/CTA) in collaboration with the medical lead and cross-functional study teams
Collaborate with cross-functional study team including clinical operations, data management and the medical lead in the review, querying and reconciliation of clinical data. Prepare data summaries and presentations as needed.
Primary clinical expert for clinical trial sites and study teams for assigned studies
Intermittent travel to clinical sites and professional meetings and congresses required
Skills/Knowledge Required - To be a suitable candidate for this role, you must have:
Bachelor's degree required; Master's degree, PhD or PharmD preferred
Minimum 4 years prior experience in related biomedical research in industry or academia
Ability to plan, develop, and execute early clinical development oncology and/or hematology studies including analysis, interpreting, and reporting results
Applicants should have strong leadership skills, yet be able to work effectively in a team environment
Must be available on Eastern Standard/Daylight hours
Excellent communication and presentation skills are essential
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.