Senior Pipeline Medical Science Liaison, CVRM Pipeline (FL/PR, GA, AL)
Company: Genentech
Location: Birmingham
Posted on: May 3, 2025
Job Description:
The PositionThe OpportunityThe Therapeutic Area Pipeline Medical
Science Liaison (TA Pipeline MSL) is a credible field medical
partner responsible for providing clinical, scientific and other
relevant information related to disease states and the appropriate
utilization of Genentech medicines in the TA pipeline (and
TA-related approved medicines, as appropriate). This field-based
position will engage with healthcare providers, clinical study
staff, therapeutic area experts (TAEs), population health decision
makers, and patient thought leaders within their region(s), to
further patient outcomes aligned with the overarching objectives of
Genentech. In collaboration with home office and regional partners,
TA Pipeline MSLs are accountable for comprehensive activities
focused on delivering a successful clinical development program
including, but not limited to: clinical trial recruitment focused
activities, competitive intelligence, Congress support,
professional society engagement, and TA landscaping. In addition,
TA Pipeline MSLs may be responsible for covering multiple pipeline
medicines, as well as engaging in broad clinical and scientific
discussions resulting in rich customer insights shared with key
stakeholders across the organization.Preferred States of Residence:
FL/PR, GA, ALKey Responsibilities
- Ensure end-to-end customer experience for TA specific customers
in the region.
- Demonstrate deep scientific expertise in assigned
molecules/products and therapeutic areas to exchange relevant
information with thought leaders and healthcare decision
makers.
- Assist with Phase I - IV sponsored and supported clinical
trials, health economic outcomes research, and other TA specific
medical collaborations; provide clinical expertise overview of
performance metrics and feedback regarding operational management
of clinical trials to ensure optimal site selection and
performance. Fully understands site infrastructure and ways of
working to best co-create and monitor clinical trial processes.
Supports start-up, recruitment, and retention in assigned
geographies. Provides critical collaboration with CRO personnel, as
appropriate, and in pre-specified manner.
- Build and leverage relationships with key external scientific
and medical customers to understand evolving healthcare
trends.
- Having proficiency in topics beyond scientific exchange, such
as value/cost of care discussions, integrated evidence planning,
and strategic medical planning, among other related topics.
- Continuous learning within the therapeutic area, active
participation in upskilling programs, and adherence to guidelines
and procedures.Who you areRequired Qualifications & Experience
- Advanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN,
NP, PA etc.). BSN with extensive field medical experience with a
pharmaceutical company.
- Minimum of 5 years related work experience (clinical, managed
care, or industry experience).
- Proficiency in GCP (Good Clinical Practice) and ICH
(International Conference on Harmonization of Technical
Requirements for Registration of Pharmaceuticals for Human
Use).
- Relevant therapeutic area knowledge, comprehensive
understanding of product and safety profiles, and familiarity with
managed care, health economics, reimbursement, and legal and
regulatory landscape in the pharmaceutical/biotechnology
industry.Preferred Experience
- Prior experience as a field medical science liaison.
- 2 + years' clinical research experience (either in industry or
in another, related setting).
- 2 + years' experience in therapy area.
- In-depth knowledge of clinical development programs and
clinical trial management.
- Prior experience working in heavily matrixed organizations
interfacing with clinical operations, clinical development and
medical affairs organizations.Location and Travel Requirements
- Business travel, by air or car, is required for regular
external business meetings with customers and intermittent internal
company meetings (up to 70% of time).
- This position requires significant use of a company-provided
car to perform the essential duties and responsibilities of the
role. As a result, Genentech, Inc. (Company) from time to time will
check your motor vehicle record for purposes of determining your
eligibility for driving a Company vehicle or driving any vehicle on
Company business.
- Applicants should reside within 30 miles of a major airport and
should reside within 50 miles of the established territory.
Preference will be given to applicants who reside within preferred
states of residence listed above.The expected salary range for this
position is $157,100-291,700. Actual pay will be determined based
on experience, qualifications, geographic location, and other
job-related factors permitted by law. A discretionary annual bonus
may be available based on individual and Company performance. This
position also qualifies for the benefits detailed at the link
provided below.Relocation benefits are not available for this job
posting.This is a field based role.Genentech is an equal
opportunity employer. It is our policy and practice to employ,
promote, and otherwise treat any and all employees and applicants
on the basis of merit, qualifications, and competence. The
company's policy prohibits unlawful discrimination, including but
not limited to, discrimination on the basis of Protected Veteran
status, individuals with disabilities status, and consistent with
all federal, state, or local laws.If you have a disability and need
an accommodation in relation to the online application process,
please contact us by completing this form .
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Keywords: Genentech, Birmingham , Senior Pipeline Medical Science Liaison, CVRM Pipeline (FL/PR, GA, AL), Healthcare , Birmingham, Alabama
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