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Job Details

Senior/Medical Science Liaison Respiratory AZ NM UT CO WY NE SD ND

Company name
Genentech, Inc.

Denver, CO

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In this position, you will be primarily accountable for consistently, effectively:

Representing the assigned molecules/products, franchise(s) and overall therapeutic area(s) to the highest ethical andprofessional standards and in accordance with guidelines, direction and key marketing strategies

Responding to on- and off-label questions with the highest integrity, compliance and adherence to legal, regulatory andGenentech guidelines, policies & procedures

Building and cultivating important working relationships internally and externally

Providing clinical expertise and feedback regarding operational management that effectively and efficiently guides clinicaltrials, other studies and investigations

Providing clinical expertise in the development, management and maintenance of clinical and scientific communications,including research, publications, and educational materials, meeting/event presentations and information, etc.

Actively and effectively participating in various internal and external clinical and scientific education programs, meetings,presentations and other forums; providing in-depth clinical and operational expertise and insights regarding the assignedmolecules/products, franchise(s), and overall therapeutic area(s)

Completing special projects when self-identified or assigned

Ensuring assigned goals and objectives are met and that assigned projects and other work are completed on time, tohigh standards and within budget

Example Responsibilities

In this position, you will contribute by:


Working with manager, peers, other partners and stakeholders in the development and alignment of medical plan tactics atthe regional and local MSL levels

Participating in a variety of cross-functional tactical planning meetings, reviews and discussions

As assigned, supporting your manager, medical directors, and other peers in gathering information, analyses, researchand reporting to support national, regional, and local tactical planning

With assistance from your manager, using national and regional medical plans for the assigned molecules/products todevelop and align the tactical plan for your geography of responsibility

Providing input to manager regarding travel, budget and other resource requirements to meet or exceed assigned goalsand objectives

Building and cultivating relationships with internal cross-functional partners, such as Franchise Sales, Franchise Marketing,Managed Care & Customer Operations, Thought Leader Services, Pharmaceutical Research and Early Development,Product Development, Clinical Operations, Commercial Operations and other Medical Affairs groups

Building and cultivating relationships with the local scientific and medical communities, including study site clinical researchstaff, clinical investigators, physicians, other healthcare professionals, as well as regional thought leaders


As appropriate, support design and development of clinical trials, other studies and investigations

Support Clinical Operations with Phase III studies, by providing clinical support at investigator sites

Evaluate, review and propose, when and where appropriate, revisions to protocols in support of the development and/or medical strategies of the assigned product(s). As and when approved, undertake the necessary revisions to protocols,ensuring full compliance with all established procedures and guidelines, as well as appropriate communication to otherinvolved/impacted colleagues and/or external parties

Work with a host of cross-functional partners to develop plans and tactics for implementation and completion ofclinical trials, studies and other investigations. Includes plans for developing and recruiting for patient registries, clinicaland scientific communications, publications, clinical and scientific education, advisory boards, clinical and scientificcongresses, other conferences and meetings, etc.

Work with Medical Communications and Publication Planning to develop, disseminate and manage calendars andtimelines for clinical and scientific communications, publication plans and other relevant research, data, information andcommunications for assigned molecules/products


Maintain the highest standards and levels of scientific, clinical and technical expertise in the specific therapeutic area(s)of assignment; reviewing and keeping updated on scientific/medical journals and other relevant publications, attendingscientific, clinical, commercial and other key meetings, forums, venues, etc., as well as continuous communication andeffective partnering with various Genentech and Roche groups

As assigned, complete special projects


Company info

Genentech, Inc.
Website :

Company Profile
Considered the founder of the industry, Genentech, now a member of the Roche Group, has been delivering on the promise of biotechnology for over 35 years. At Genentech, we use human genetic information to discover, develop, manufacture and commercialize medicines to treat patients with serious or life-threatening medical conditions. Today, we are among the world's leading biotech companies, with multiple products on the market and a promising development pipeline.

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