Associate Medical Director

Oncology/Molecular Pathology Position

The incumbent, with expertise in Oncology and/or Molecular Pathology, will analyze and understand the laboratory and clinical aspect of high complexity tests, as offered by Agendia, Inc., in order to select areas of tumor for molecular analyses, interpret immunohistochemical tests, and explain the clinical and pathological significance of his/her interpretations. This is a hybrid position.

Reports to Senior Medical Director, Laboratory Services. Cooperates with relevant departments (such as Laboratory Operations, QA, and commercial teams) within Agendia. Participates in department meetings, project meetings, working groups, and project groups.

Essential duties and responsibilities include conducting histopathologic examination of submitted specimens to assess their adequacy for testing and make recommendations when limited specimen is available. Provide interpretation of immunohistochemical (IHC) stains as needed. Review batch and instrument quality control IHC stains as needed. Participate in day-to-day operations, including sign-out of Agendia's genomic assays with full-time availability to interact with clients for pre-analytical, analytical, and post-analytical questions. Provide expertise and assistance to technologists and technicians to resolve case issues. Serve as delegated Clinical Consultant when assigned by Senior Medical Director. Works closely with clinical and administrative staff to ensure the highest standards of turnaround time, quality, and customer service are maintained. Assist with management of the Pathology Report Data Entry process. Follow established policies, procedures, continuous quality improvement objectives, safety, environmental, and/or control standards. Assist with clinical studies sponsored by Agendia. Assist as needed to perform other related duties and special projects as required.

Key contacts include working closely with Laboratory Operations, Customer Service, Product Support, Marketing, and all possible interfacing groups or teams internally. Externally, works with ordering physicians, pathology institutions, and regulatory agencies.

Education and experience requirements include being a M.D. or D.O. with certification in Anatomic Pathology (AP) or Anatomic/Clinical Pathology (AP/CP). Active unrestricted Medical License to practice in the state of California is required. Medical License to practice in the state of New York is desired. Additional subspecialty education in Surgical Pathology or fellowship training (with Board eligibility or certification) in Molecular Genetic Pathology is preferred but not required. Trained in pathology residency programs in US (fellowship preferred), with at least 1 year of experience in clinical practice or industry. 5+ years clinical and laboratory experience. Must have 5+ years of Anatomical Pathology Experience. Experience with Molecular Diagnostics highly preferred. Experience in Breast Cancer Diagnostics highly preferred.

Desired experience/skills include Certificate of Qualification in Histopathology and/or Molecular and Cellular Tumor Markers from New York State Department of Health.

Knowledge, skills, and abilities (KSA's) include knowledge and experience using diagnostic equipment, such as conventional or digital microscope. High degree of care and attention with strict adherence to defined clinical testing protocols. Demonstrated skills and high level of attention to detail in technical data interpretation and ability to troubleshoot. Skill and ability to provide genomic testing support for cancer patients. Skill in utilizing customary computer programs and ability to learn internal software programs for diagnostic purposes. Skill and ability to communicate verbally and in writing with all levels of staff. Skill and ability to learn and collaborate with others in a complex, multi-functional environment. Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area. Skill and ability to evaluate, interpret and present highly complex data for a series of studies (prospective and retrospective). Strong communication & presentation skills. Ability to summarize and communicate the key points for others to effectively and expeditiously make important business decisions. Demonstrated organizational skills to manage multiple projects simultaneously. Ability to work independently. Working knowledge of FDA regulations and the clinical laboratory regulatory environment are a plus. Must be able to work a hybrid schedule.

Behavioural competencies/desired skills include exhibiting professional maturity, confidence, and competence. Sound and accurate judgment. Sets and achieves challenging goals. Demonstrates persistence to overcome obstacles. Applies creative, out-of-the box thinking to overcoming obstacles and taking advantage of opportunities in the marketplace. Works well in a fast-paced environment filled with many priorities and time.

Working environment includes established ADA (Americans with Disabilities Act) requirements. Working conditions (inside or outside the office). Exposure to chemicals. A majority of the position may be non-sedentary. Adheres to Department Specific Safety Guidelines.

Ability to travel domestically, up to 10%. Other duties as required.