Senior Pipeline Medical Science Liaison, CVRM Pipeline (FL/PR, GA, AL) Position Available In Jefferson, Alabama

Job Description:

The PositionThe OpportunityThe Therapeutic Area Pipeline MedicalScience Liaison (TA Pipeline MSL) is a credible field medicalpartner responsible for providing clinical, scientific and otherrelevant information related to disease states and the appropriateutilization of Genentech medicines in the TA pipeline (andTA-related approved medicines, as appropriate). This field-basedposition will engage with healthcare providers, clinical studystaff, therapeutic area experts (TAEs), population health decisionmakers, and patient thought leaders within their region(s), tofurther patient outcomes aligned with the overarching objectives ofGenentech. In collaboration with home office and regional partners,TA Pipeline MSLs are accountable for comprehensive activitiesfocused on delivering a successful clinical development programincluding, but not limited to: clinical trial recruitment focusedactivities, competitive intelligence, Congress support,professional society engagement, and TA landscaping. In addition,TA Pipeline MSLs may be responsible for covering multiple pipelinemedicines, as well as engaging in broad clinical and scientificdiscussions resulting in rich customer insights shared with keystakeholders across the organization.

Preferred States of Residence:

FL/PR, GA, ALKey Responsibilities Ensure end-to-end customer experience for TA specific customersin the region. Demonstrate deep scientific expertise in assignedmolecules/products and therapeutic areas to exchange relevantinformation with thought leaders and healthcare decisionmakers. Assist with Phase I – IV sponsored and supported clinicaltrials, health economic outcomes research, and other TA specificmedical collaborations; provide clinical expertise overview ofperformance metrics and feedback regarding operational managementof clinical trials to ensure optimal site selection andperformance. Fully understands site infrastructure and ways ofworking to best co-create and monitor clinical trial processes.

Supports start-up, recruitment, and retention in assignedgeographies. Provides critical collaboration with CRO personnel, asappropriate, and in pre-specified manner. Build and leverage relationships with key external scientificand medical customers to understand evolving healthcaretrends. Having proficiency in topics beyond scientific exchange, suchas value/cost of care discussions, integrated evidence planning,and strategic medical planning, among other related topics. Continuous learning within the therapeutic area, activeparticipation in upskilling programs, and adherence to guidelinesand 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 apharmaceutical company. Minimum of 5 years related work experience (clinical, managedcare, or industry experience). Proficiency in GCP (Good Clinical Practice) and ICH(International Conference on Harmonization of TechnicalRequirements for Registration of Pharmaceuticals for HumanUse). Relevant therapeutic area knowledge, comprehensiveunderstanding of product and safety profiles, and familiarity withmanaged care, health economics, reimbursement, and legal andregulatory landscape in the pharmaceutical/biotechnologyindustry.

Preferred Experience Prior experience as a field medical science liaison. 2 + years’ clinical research experience (either in industry orin another, related setting). 2 + years’ experience in therapy area. In-depth knowledge of clinical development programs andclinical trial management. Prior experience working in heavily matrixed organizationsinterfacing with clinical operations, clinical development andmedical affairs organizations.

Location and Travel Requirements Business travel, by air or car, is required for regularexternal business meetings with customers and intermittent internalcompany meetings (up to 70% of time). This position requires significant use of a company-providedcar to perform the essential duties and responsibilities of therole. As a result, Genentech, Inc. (Company) from time to time willcheck your motor vehicle record for purposes of determining youreligibility for driving a Company vehicle or driving any vehicle onCompany business. Applicants should reside within 30 miles of a major airport andshould reside within 50 miles of the established territory.

Preference will be given to applicants who reside within preferredstates of residence listed above.

The expected salary range for thisposition is $157,100-291,700. Actual pay will be determined basedon experience, qualifications, geographic location, and otherjob-related factors permitted by law. A discretionary annual bonusmay be available based on individual and Company performance. Thisposition also qualifies for the benefits detailed at the linkprovided below.

Relocation benefits are not available for this jobposting.

This is a field based role.

Genentech is an equalopportunity employer. It is our policy and practice to employ,promote, and otherwise treat any and all employees and applicantson the basis of merit, qualifications, and competence. Thecompany’s policy prohibits unlawful discrimination, including butnot limited to, discrimination on the basis of Protected Veteranstatus, individuals with disabilities status, and consistent withall federal, state, or local laws.

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