Medical Science Liaison, Hemophilia & Non-Malignant Hematology- West 1: CA-HI, Seattle & AK, Western OR, Eastern WA/OR- GENENTECH Honolulu

Title Medical Science Liaison, Hemophilia & Non-malignant Hematology- West 1: Ca-hi, Seattle & Ak, Western Or, Eastern Wa/or-
Date 2020
City Honolulu

Short Description :

Vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business Prior experience as a field medical science liaison is preferred Build and cultivate important working relationships across field partners to ,…

Full Description :

The Position
Position Overview:
The Therapeutic Area Medical Science Liaison (TA MSL) is a credible scientific partner responsible for providing clinical and health economic information related to disease states and the appropriate utilization of medicines (approved and pipeline). This field-based position will engage with healthcare providers, population health decision makers, and patients within their region(s), to further patient outcomes aligned with the overarching objectives of . In collaboration with their regional partners, TA MSLs are accountable for co-creating the local medical strategy and delivering for their customers. In addition, TA MSLs may be responsible for covering multiple medicines, as well as engaging in broad scientific discussions around patient outcomes and total cost of care, resulting in rich customer insights shared with key stakeholders across the organization.
Key Responsibilities/Accountabilities:
Ensure an end to end customer experience for TA specific customers within the region
Demonstrate deep scientific expertise about assigned molecules/products, franchise(s) and overall therapeutic area(s) to exchange relevant information and insights with top tier thought leaders and healthcare decision makers within a region
Build, cultivate, and leverage relationships with key external scientific and medical customers and organizations in their region(s) to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape
Demonstrate proficiency in topics beyond scientific exchange such as value / cost of care discussions, hospitalizations, risk of progression, drug pricing pressures, reimbursement education, and AE management
Engage in continuous independent learning within the therapeutic area they represent and actively attend and participate in upskilling programs related to assigned molecules, products, disease states and relevant business topics
Respond to on and off-label questions with integrity, compliance, and adherence to legal, regulatory, and guidelines, policies & procedures
Build and cultivate important working relationships across field partners to ensure an enterprise approach when working with customers. Be accountable to the regional team to shape and execute on local medical strategies within planned timelines
Depending on regional needs and priorities, may be asked to serve in a Medical Affairs Executive Director (MED) role with specific customers
Identify and bring insights back in house to stakeholders through efficient and effective use of CRM system
Assist with Phase IIV sponsored and supported clinical trials, health economic outcomes research, other TA specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance
Share clinical and value-based expertise in the development and management of clinical and scientific communications for customers to include publications, conference data, and educational materials, as well as for internal communications and materials to be used in training and development activities
Ensure assigned goals and objectives are met and that assigned projects and other work are completed on time, with high quality, and within budget
Advanced Clinical/Science Degree required (e.g., MD, PharmD, PhD, MSN, NP, PA etc.). BSN with extensive clinical experience may be considered.
GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use) proficient
In-depth knowledge of Phase IV/post-marketing drug development is preferred
Relevant therapeutic area knowledge, dependent on customer base
Comprehensive understanding of product and safety profiles
Understanding of managed care, health economics, healthcare reimbursement, managed care customers and the distribution channels relevant to pharmaceutical/biotechnology organizations
Familiarity with the current legal and regulatory landscape pertinent to the pharmaceutical/biotechnology industry
Required Experience:
Minimum of 5 years related work experience (clinical, managed care, or industry experience)
Prior experience as a field medical science liaison is preferred
2 or more years’ clinical or health economic research experience (either in industry or in another, related setting) is preferred
2 years' experience in therapy area is preferred
Ability to learn other disease or product areas as business needs and product life cycles change
Outstanding organizational and time management skills; proven abilities to manage multiple, often complex and sometimes competing, objectives, goals and other priorities to effective and efficient conclusion
Proven track record of meeting or exceeding objectives and goals
Strong attention-to-detail
Learning mindset, open to training and becoming an expert across customer types or multiple therapeutic areas
Outstanding business acumen; knows the industry, 's business model and value proposition, key competitors and other marketplace factors/dynamics
Excellent communication and collaboration skills; exhibits professional maturity, confidence, and competence. Strong conflict resolution skills; proven ability to effectively and quickly achieve conflict resolution with affected parties and work in a cross functional environment
Knows how to summarize and communicate complex information and business objectives in a concise and effective way for important presentations and decisions
Embraces change, embodies a continuous improvement mindset, and exemplifies agile principles in day-to-day activities
In addition to passing 's background screening, the employee must submit to and pass additional background screening as required by some institutions and health facility sales accounts (additional screening requests may include but are not limited to background checks, immunization, TB, HIV, hepatitis, and drug screening)
Business travel, by air or car, is required for regular internal and external business meetings (up to 70% of time)
This position requires significant use of either a company provided or personal vehicle to perform the essential duties and responsibilities of the role. As a result, , 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
Who We Are
A member of the Roche Group, has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.
The next step is yours. To apply today, click on the "Apply online" button.
is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Careers page . Job Facts JOB FUNCTION
Medical Science Liaison COMPANY/DIVISION
Pharmaceuticals SCHEDULE
Full time JOB TYPE

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