Clinical Trial Physician, Rheumatology
Jobbeschreibung
Boudry, Neuenburg, Schweiz
Bristol-Myers Squibb
27.04.2024
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Working with UsChallenging. Meaningful. Life-changing. Those aren’t
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
transforms the lives of patients, and the careers of those who do it.
You’ll get the chance to grow and thrive through opportunities
uncommon in scale and scope, alongside high-achieving teams rich in
diversity. Take your career farther than you thought possible.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. Read
more: careers.bms.com/working-with-us.Position Summary /
ObjectiveServes as a primary source of medical accountability and
oversight for multiple clinical trials and across assetsManages Phase
1 – 3 studies, with demonstrated planning and decision making
capabilitiesProvides medical and scientific expertise to
cross-functional colleaguesMatrix management responsibilities across
internal and external networksPosition ResponsibilitiesMedical
MonitoringContributes to and is a key member of a high performing
Study Team, and may be a member of the Clinical Development Team
(CDT)Leads collaboration with CS and inputs into protocols and related
study documents, providing medical oversight in protocol
developmentHolds responsibility for site interactions in partnership
with the Clinical Scientist (CS) for medical questions and trainings
(including safety management guidelines)Holds responsibility for
assessment of key safety-related serious adverse events in partnership
with Worldwide Patient Safety and oversees safety narrativesLeads
medical review of trial data, including top line results and full set
of TLGs/TLFsFulfills GCP and compliance obligations for clinical
conduct and maintains all required trainingClinical Development
Expertise & StrategyIn collaboration with the Clinical Development
Lead, designs and develops clinical plans and protocols with a strong
strategic focus based on knowledge of asset/drug, disease area and
relevant science in order to meet regulatory and disease strategy
targetsProvides oversight and medical accountability for a group of
studies across therapeutic indicationsLeads the analysis of
benefit/risk for clinical development protocols in a matrix team
environment working with Clinical Scientists (CS)Partners with CS to
support executional delivery of studies (e.g., site activation,
enrollment status, as well as adjudication for protocol violations,
significant, non-significant deviations etc.)Identifies and builds
relationships with principal investigators. Identifies and cultivates
thought leaders in order to gain their inputs on emerging science in
drug and biomarker research, disease knowledge, and design of clinical
development studies and programsMaintains a strong medical/scientific
reputation within the disease area. Has in-depth knowledge of
etiology, natural history, diagnosis, and treatment of the disorder.
Holds strong expertise in the disease area by attending scientific
conferences and ongoing review of the literatureKeeps abreast of
development and regulatory issues related to other competitive or
relevant compounds in development and how our portfolio fits into the
competitive landscapeProvides ongoing medical education in partnership
with collaborating Clinical Scientists to allow for protocol-specific
training, supporting the study team, investigators, and othersHealth
Authority Interactions & PublicationsContributes to and serves as
medical point of expertise in key Health Authority interactions and
advisory board meetingsAuthors/drafts clinical content for CSRs,
regulatory reports, briefing books and submission documents to support
closure, clinical narratives, reporting and filling of the studyDegree
RequirementsMD required (or ex-US equivalent)Subspecialty training in
applicable therapeutic area (rheumatology, immunology, cell therapy)
highly desiredExperience Requirements5 or more years of industry or
strong relevant scientific/medical experience in global clinical
trials and drug developmentHA interactions and submission hands-on
experience is an advantage Key Competency RequirementsExpertise in
drug development processExpertise in the components needed to execute
an effective clinical plan and protocolsExpertise in scientific
methods to test hypotheses, including statistical design, analysis,
and interpretation of complex dataAbility to communicate information
clearly and lead presentations in scientific and clinical
settingsProven ability to work effectively in matrix environment and
across therapeutic indications and franchisesTravel RequiredDomestic
and International travel may be requiredIf you come across a role that
intrigues you but doesn’t perfectly line up with your resume, we
encourage you to apply anyway. You could be one step away from work
that will transform your life and career.Uniquely Interesting Work,
Life-changing CareersWith a single vision as inspiring as
“Transforming patients’ lives through science ”, every BMS employee
plays an integral role in work that goes far beyond ordinary. Each of
us is empowered to apply our individual talents and unique
perspectives in an inclusive culture, promoting diversity in clinical
trials, while our shared values of passion, innovation, urgency,
accountability, inclusion and integrity bring out the highest
potential of each of our colleagues.On-site ProtocolPhysical presence
at the BMS worksite or physical presence in the field is a necessary
job function of this role, which the Company deems critical to
collaboration, innovation, productivity, employee well-being and
engagement, and it enhances the Company culture.BMS is dedicated to
ensuring that people with disabilities can excel through a transparent
recruitment process, reasonable workplace accommodations/adjustments
and ongoing support in their roles. Applicants can request a
reasonable workplace accommodation/adjustment prior to accepting a job
offer. If you require reasonable accommodations/adjustments in
completing this application, or in any part of the recruitment
process, direct your inquiries to Visit
careers.bms.com/eeo-accessibility to access our complete Equal
Employment Opportunity statement.BMS cares about your well-being and
the well-being of our staff, customers, patients, and communities. As
a result, the Company strongly recommends that all employees be fully
vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS
will consider for employment qualified applicants with arrest and
conviction records, pursuant to applicable laws in your area.Any data
processed in connection with role applications will be treated in
accordance with applicable data privacy policies and regulations.