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$160k–$210k/yr
Full-time
postgraduate degree
Posted just now
~40 hrs/week
Remote in Los Angeles, California, United States
Responsibilities
The Medical Science Liaison will serve as a company spokesperson, identifying and managing relationships with key opinion leaders while providing scientific expertise on clinical programs and products. They will also support medical marketing, clinical trial strategy, and regulatory activities to ensure alignment with company business goals.
Requirements
Candidates must hold an advanced degree (PharmD, MD, PhD) or a clinical license with a Master's degree, along with at least 3 years of experience in oncology. Strong communication skills and the ability to travel up to 75% of the time are essential for this role.
Full job description
Description
**Territory will encompass: Los Angeles to Washington State
AIM OF THE POSITION
The Medical Science Liaison l/ll (MSL)-US, works as member of a medical/scientific team. This individual will function, in part, as a company spokesperson on clinical programs, clinical trials, and marketing functions that require clinical/medical translation. This scope of work will include interfaces with the commercial team and various appropriate clients of Agendia. The MSLl/ll US identifies and develops relationships with key opinion leaders (KOLs) and highly accomplished physicians whose views on breast cancer treatment tend to influence other doctors. Provides detailed knowledge of the organization's new/current products and services. Distributes scientific information and resources to the KOLs. Assist in the development and integration of research initiatives and product and customer strategies. The MSL l/ll-US help facilitate the ongoing activities of medical communications, clinical trial functions and facilitate the medical marketing programs. The MSL l/ll -US will participate in the planning and implementation of medical marketing, clinical registry programs and customer service functions aligned to the strategic business needs of the company. In addition, the MSL l/ll-US will help represent the company at sales meetings, conferences, client clinical presentations and patient advocacy functions. The MSL l/ll-US will assist in the analysis and preparation of clinical trials data and registry data for abstract development and formal presentation either poster or oral as well as assist in the preparation of peer-reviewed manuscripts of scientific and medical data for publication. MSL l/ll will work closely with VP Clinical affairs on the medical aspects of reimbursement and tech assessments of Agendia’s products
POSITION WITHIN THE ORGANIZATION
1. Sr. Director, Medical Science Liaisons
2. Cooperates with, Medical Affairs, Sales, Lab Ops, Customer Care, Marketing, Clinical Affairs, R & D, QA/RA, etc.
3. Participates in:
Department meetings
Project meetings (with both internal and external stakeholders)
Working groups
Portfolio meetings
Requirements
ESSENTIAL DUTIES AND RESPONSIBILITIES
Identify, target, educate and manage accounts in the assigned territory including hospitals, pathology groups, oncologists, and surgeons on Agendia’s products.
Interfaces with current and new collaborations within the oncology field as required
Works with managed care in a support role to develop and refine required clinical / medical documentation to support medical policy for reimbursement.
Provides support to members of the management team involved in regulatory affairs as required in the preparation of documents and material for presentation.
Support Agendia’s Sales and Marketing efforts (25%), Clinical Trial strategy and clinical utility data development (25%), regulatory and reimbursement activities (25%) and client services and support activities (25%).
Contribute medical and clinical input to the new product development process.
Provide support to the VP Medical Affairs for medical marketing plans for product development in cooperation with the Sales and Marketing department
Provide support to the VP Medical Affairs for the development, and presentation of medical, clinical, and scientific materials to all stakeholders with a significant cooperation with the sales and marketing organizations.
Present programs to educate appropriate customers about Agendia’s diagnostic product offerings such as scientific publications, account in-services, WebEx sessions, scientific presentations, etc.
Provide statistical and analytic support for medical input for the development of clinical trials/research, data collection, safety, and medical information programs
Assist in the design and implementation of clinical trials and interpretation of results
Participate in the assessment of clinical data and, in collaboration with Marketing and Regulatory:
Assist in developing product specific information and communication strategies.
Cultivate and maintain open and positive relationships with key thought leaders and customers:
Assist where appropriate with physicians and patients regarding data interpretation
Present data as appropriate to a wide range of audiences including but not limited to physicians, hospital administrators, and payers within the US.
Demonstrates deep knowledge competency; stays abreast of trends and new information in the science area, as well as the profession at large.
Serve as technical/scientific subject matter resource to Agendia commercial personnel, if requested
The above listing represents the general duties considered essential functions of the job and is not to be considered a detailed description of all the work requirements that may be inherent in the position.
KEY CONTACTS
Internal
o Works closely with:o Medical Affairso Sales, Clinical Affairs, R&D, QA/RA, Lab Ops, and has interactions with all departments company wide
External
o Works with physicians, doctors, KOLs, patients, managed care personnel business associates, vendors and regulatory agencies
EDUCATION AND EXPERIENCE REQUIREMENTS
EDUCATION
Advanced degree (PharmD, MD, PhD or equivalent) with a minimum of 1-3 years’ experience in Oncology. Solid tumor experience preferred.
OR
License (RN, NP, CNP, PA or equivalent) with a minimum of a Master’s Degree (or equivalent) and a minimum of 3 years’ experience in Oncology, breast cancer experience preferred.
EXPERIENCE
A minimum of 3 years of experience as a MSL or comparable industry or clinical role (customer facing)
Experience in the presentation and/or interpretation of scientific or clinical research publications.
Experience in establishing strong, collaborative working relationships with internal stakeholder functions (e.g.e.g., Sales, Marketing, Regulatory, R&D) and external customers
KNOWLEDGE, SKILLS AND ABILITIES (KSA’S)Specific Knowledge Required:
· Knowledge of geography and key opinion leaders preferred
· Excellent verbal & written communication skills as well as interpersonal skills
· Understanding of regulatory requirements for field-based personnel
· Ability to collaborate with internal colleagues in sales, marketing, and managed care accounts
Ability to summarize complex scientific information and present in a clear, concise, confident, and scientifically accurate and balanced manner to a range of audiences across various modalities (1:1, video, group presentations, etc.)
· Ability and willingness to travel at least 75% of workdays required
· Proficiency in PowerPoint and Excel skills required
· Ability to work independently while adhering to Medical Affairs strategic direction
· Ability to anticipate, organize and plan multiple changing priorities
· Knowledge of relevant healthcare systems, medical landscape, regulatory and payor environment, public health, and industry trends
· Proficiency in digital tools
BEHAVIOURAL COMPETENCIES/DESIRED SKILLS
Judgment - Displays willingness to make decisions and participate in upper management decision-making; exhibits sound and accurate judgment.
Motivation - Sets and achieves challenging goals; demonstrates persistence and overcomes obstacles.
Creative Problem Solving - Applies creative, out-of-the box thinking to overcoming obstacles and taking advantage of opportunities in the marketplace.
Time management - Works well in a fast-paced environment filled with many priorities and varying timelines for product launch.
Superior leadership skills that lead to the development of highly functioning marketing organization through motivation and development of personnel.
Self-starter with an entrepreneurial spirit and understanding of big picture with attention to detail.
MammaPrint® + BluePrint® provides you with actionable insights throughout your patient’s breast cancer journey.
Industry
Biotechnology
Company size
51-200 employees
Founded
2003
Headquarters
Irvine, CA
LinkedIn followers
22,225
Total funding
$182M
Agendia, a precision oncology company, helps physicians and patients make personalized treatment decisions in early-stage breast cancer. MammaPrint® (MP), 70-gene breast cancer recurrence assay, is the only FDA-cleared (microarray) risk of recurrence test and is CE marked (IVDR-certified). BluePrint®(BP), 80-gene molecular subtyping assay, evaluates the underlying biology of a tumor to determine growth drivers. MP+BP are commercially available genomic tests, supported by clinical, guideline, peer-reviewed, and real-world evidence. They can be ordered on core biopsies or surgical specimens.*
*FDA Intended Use: the test is performed for breast cancer patients with Stage I or Stage II disease with tumor size ≤5.0cm and lymph node negative. The MP FFPE result is indicated for use by physicians as a prognostic marker only, along with other clinicopathological factors. Coverage criteria for majority of US health plans include early-stage breast cancer, tumor size less than or equal to 5.0cm (≤5.0cm), up to 3 positive lymph nodes, independent of receptor status, as validated in the 6,693 patient MINDACT trial. IVDR-CE mark Intended Use: you are a female breast cancer patient with Stage I or Stage II disease who is lymph node negative or lymph node positive with up to 3 positive nodes and for patients with stage III disease. The MP FFPE result is indicated for use by physicians and should be interpreted with other clinico-pathological factors. BP was developed and its performance characteristics determined by Agendia. It has not been cleared or approved by the US FDA, which determined that such clearance or approval is not necessary. This test is used for clinical purposes. It should not be regarded as investigational or for research. This test was performed at Agendia, Inc (05D1089250), which is certified under CLIA as qualified to perform high-complexity clinical laboratory testing. It is CE-marked for use in Europe. Social media policy: agendia.com/legal-compliance
Offices: 22 Morgan, Irvine, CA 92618, US
Breast Cancer and Genomic AssaysHealth DiagnosticsHealth CareBiotechnologyLife ScienceGeneticsMedical
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