- Identify, develop and/or maintain strong, collaborative working relationships with premier cancer center KOL champions, to promote understanding and adoption of our novel diagnostic technologies.
- Collaborate with commercial, market access, and medical affairs to set the agenda for and design clinical oncology research initiatives including collaborating with external KOLs to define publication strategies.
- Identify and help draft study protocols and publication plans, including drafting/first authoring of multiple abstracts and publications with external KOL coauthors.
- Manage Medical Science Liaison and Clinical Oncology Specialist teams to develop KOL champions at NCI centers and large oncology group strategic partners.
- Lead in major investigator-initiated, multicenter studies that expand our indications through validation and outcomes assessment.
- Stay updated on developments in clinical oncology including new applications, clinical trial data, presentations and publications on the clinical utility of molecular testing, emerging biomarkers that affect the use of current testing and the development of new test modalities.
- Provide leadership of educational and client support for the sales team and the managed care team in the area of oncology.
- Represent Quest at national and international oncology conferences and at focused meetings in medical, radiological and surgical oncology by collaboratively preparing abstracts and presenting data.
- Support other Quest medical affairs directors who are responsible for building and managing scientific and clinical community relationships and, upon request, helping mediate resolution of client queries.
- Work with the BioPharma team in collaborative research efforts with pharmaceutical companies around somatic oncology.
- Work with the Business Development team in collaborative research efforts with large health care systems in implementing cancer management.
- M.D. or D.O. with board certification in Hematology/Oncology
- A minimum 6 years' experience providing clinical oncology patient care in a setting that utilizes molecular oncology testing to inform management and guide therapy.
- Comprehensive knowledge of clinical trials that address the use of molecular genetic testing in oncology care.
- Experience participating and leading molecular tumor boards where molecular oncology testing is presented and discussed.
- Excellent verbal and written communication skills.
- Capable of networking both nationally and internationally with oncology colleagues.
- Previous experience, typically obtained through PhD or postdoctoral work, in laboratory-based molecular oncology research such that the participant will be familiar with the molecular genetic DNA tools used in oncology such as next-generation sequencing, tumor sequencing for therapy selection, and circulating tumor DNA analysis.
- Service on one or more committees of a professional oncology society or engagement in the development of clinical guidelines and standards of care.
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Medical Director - Baltimore, United States - Quest Diagnostics
Description
Overview:
Medical Director, Molecular Oncology
The Medical Director for Molecular Oncology is a senior position for a physician with both laboratory and clinical experience who will serve as an expert on the clinical use of somatic molecular testing in cancer. The ideal candidate should have experience with clinical management of patients with cancer and understand the oncologists needs, experience and expectations concerning the use of somatic genetic testing in the clinic.
The Medical Director for Molecular Oncology will have responsibility for leading clinical research efforts directed towards developing projects that assess the clinical utility of our somatic and circulating tumor DNA testing platforms and establishing the scientific credibility of our test offerings to outside stakeholders in support of our commercial efforts. To achieve this mission, the Oncology Molecular Medical Director role requires an appreciation of current and future clinical trends, standards of care, critical trials being carried out by others and third-party reimbursement issues. The Director will pursue impactful collaborations and publications in close coordination with Medical Scientific Affairs, the Oncology Product team and Market Access departments. The director will share his/her clinical knowledge and experience with the Development team in order to advise the team on current product revisions and future product development.
The role will be supported by the Chief Medical Officer.
The Director will serve as the primary consultant in oncology internally to the commercial and marketing teams and externally to physicians, professional societies, health insurers, and patients. Activities will include scientific educational presentations at conferences and other venues and communication with clients on Quest Diagnostics Molecular Oncology test offerings in the somatic oncology space. The individual must be able to have productive peer-to-peer relationships as an honest, credible partner in healthcare, nurturing positive relationships with oncology KOLs and practicing clinicians.
Responsibilities:Preferred Work Experience:
Interested Parties Contact:
Talent Acquisition Partner, Executive and Medical Recruitment
EEO:Quest Diagnostics is an equal employment opportunity employer. Our policy is to recruit, hire and promote qualified individuals without regard to race, color, religion, sex, age, national origin, disability, veteran status, sexual orientation, gender identity, or any other status protected by state or local law. Quest Diagnostics observes minimum age requirements established by federal, state and/or local laws, and will ask an applicant for verification when deemed necessary.