Molecular Diagnostics Medical Science Liaison – Liquid Biopsy & Minimal Residual Disease - Haystack Oncology

• MSL must demonstrate in-depth knowledge of the Women’s Health and Oncology therapeutic area. MSLs posses the ability to translate this information and data into high quality medical dialogue.
• MSL must possess a sophisticated understanding of the pharmaceutical, diagnostic and healthcare industry including commercial, and government payer strategies, and the evolving healthcare delivery models.
• MSL delivers presentations to health care decision makers responding to unsolicited questions using relevant and approved materials as per legal guidelines
• MSL may support company initiated trials by interacting with primary investigators, assisting in site identification and screenings, and delivering disease education using approved resources.
• MSLs may also support data generation activities including participating in reviews of Investigator initiated proposals.
• Other activities may include identification and training of contracted speakers or internal team members if alignment with medical plan and test life cycle needs.
• MSL will identify, collect and communicate insights to address competitive medical information in addition to insights on trends and changes affecting the regulatory and payer environment used to
• develop medical strategies.
• Contributes to the development of Medical Brand Plans and Strategies by communicating his or her medical insight and knowledge derived from Expert Physicians, other Healthcare providers or scientific publications about the product or disease area, in particular with reference to patients’ needs and treatment trends.
• Fully understands and complies with Quest Diagnostics medical and corporate SOP’s.
• Identifies potential investigators for Quest Diagnostics initiated clinical trials utilizing approved resources. Provides support to the
• Clinical Site Manager, as requested and approved by the appropriate clinical oversight committees, for site support activities relating to the conduct of a Quest Diagnostics initiated clinical trial (e.g., recruitment support). 
• Facilitates the submission process of investigators’ proposals for clinical trials if support is requested, in accordance with Company Policies, and applicable laws, regulations and ethical standards.
• Adheres to the US Compliance Code of Conduct. Certifies against all required compliance training.
• Conveys a clear message on laws, regulations, and ethical standards to both internal and external customers.
• Develops an understanding of and complies with all GMA SOPs, the OIG Guidance, the CLIA requirements, ICH, GCP, and relevant FDA laws and regulations (certify completion where required).  Alerts management to possible compliance issues.
• MSLs fully comply with all company policies and applicable laws, regulations and ethical standards

Required Work Experience

• Clinical experience in Women’s Health and Oncology or with a broad medical background.
• Minimum of 4 years working in a clinical, diagnostics or pharmaceutical environment (excludes post doc education).

Preferred Work Experience

N/A

Physical and Mental Requirements

• Ability to sit or stand for long periods of time
• Position is field based; MSL is required to live in the territory which they manage or within 50 miles of the territory borders.

Knowledge

• In depth knowledge of Women’s Health and Oncology disease area, including key scientific publications
• Understanding of clinical research principles
• Understanding of the US Healthcare system, the diagnostics/pharmaceutical industry and clinical and health economic practices in the US.

Skills