Senior Clinical Scientist (Assoc. Dir.)
Company: Bristol-Myers Squibb
Location: Princeton
Posted on: May 8, 2024
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Job Description:
Working with UsChallenging.
Interested in this role You can find all the relevant information
in the description below.
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.Functional Area
DescriptionThe Senior Clinical Scientist reports through the
Clinical Science function which provides scientific expertise
necessary to design and deliver clinical studies and
programs.Position Summary / ObjectiveResponsible for
implementation, planning, and execution of assigned clinical trial
activities.
Serves as Clinical Trial Lead for one or more trialsSuccessfully
leads, plans, and executes trial level activities for multiple
trials with minimal to moderate level of supervisionProvides
scientific and clinical leadership to team of supporting Clinical
Scientists (matrix leadership)Co-Leads study team meetings in
partnership with GDO protocol manager; and collaborate 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)Position ResponsibilitiesMaintain a thorough
understanding of assigned protocols and protocol requirements;
educate supporting team membersPlan and lead the implementation all
study startup/conduct/close-out activities as applicableEvaluate
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 teamClinical data trend identification; provide
trends and escalate questions to Medical MonitorDevelop clinical
narrative plan; review clinical narrativesProvision of information
required by Protocol Manager for development of trial budget, CRO
scope of work, etc.Review development of site and CRA training
materials and presentation at SIV and Investigator meetings and
support on Study committee (e.g., DMC) activitiesDrafting/review
and validation of clinical study reports (CSRs) and clinical
portions of Regulatory Documents (e.g., IB, DSUR, regulatory
responses)Collaborate and serve as primary liaison between external
partners for scientific adviceDegree RequirementsDegree in Life
Sciences (MD, PhD, Pharm D, MS, RN or other scientific field
preferred)Experience Requirements5+ 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
interpretationKnowledge of the establishment and operation of data
monitoring committees, dose review teams, and independent response
adjudication committeesKey Competency RequirementsExcellent verbal,
written, communication and interpersonal skillsMust be able to
effectively communicate and collaborate across functions and job
levelsAbility to assimilate technical information quicklyRoutinely
takes initiativeDetail-orientedStrong sense of teamwork; ability to
lead team activitiesProficient in Medical Terminology and medical
writing skillsProficient knowledge of the disease area(s), KOLs,
indication(s), compound(s) under study (including MOA, PK/PD,
biomarker & safety profile)Proficient critical thinking, problem
solving, decision making skillsUnderstanding of functional and
cross-functional relationshipsCommitment to QualityAdaptable /
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 toolsTravel
RequiredDomestic and International travel may be required.The
starting compensation for this job is a range from
$141,000-$200,000, plus incentive cash and stock opportunities
(based on eligibility).The starting pay rate takes into account
characteristics of the job, such as required skills and the where
the job is performed.Final individual compensation will be decided
based on demonstrated experience. -For more on benefits, please
visit our https://careers.bms.com/working-with-us.Eligibility for
specific benefits listed on our BMS Careers site may vary based on
the job and location.If 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 adastaffingsupport@bms.com.
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.
Keywords: Bristol-Myers Squibb, Trenton , Senior Clinical Scientist (Assoc. Dir.), Healthcare , Princeton, New Jersey
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