ABOUT US

Molecular Pathology Laboratory Network, Inc. (MPLN) and its research division Geneuity Clinical Research Services (MPLN/Geneuity) is a privately held College of American Pathologists, New York State Department of Health and ISO15189 accredited laboratory. We offer molecular pathology diagnostic laboratory and contract clinical research services specializing in oncology, infectious disease, women's health, and clinical trials.

With over 30 years of experience in the CAP/CLIA diagnostic laboratory and 15 years supporting oncology clinical trials as a contract research organization, our company is in line for significant, continued growth.

GENERAL SUMMARY OF DUTIES:

The Genomics Scientist is responsible for corporate leadership, vision, strategy, and portfolio planning around new and emerging human genomic technologies and next-generation sequencing. The Genomics Scientist provides leadership through a strong blend of technical expertise, diagnostic and/or pharmaceutical experience, and business acumen. The Genomics Scientist fosters relationships with a variety of strategic partners related to the genomics business and effectively leads the internal validation team to the successful completion of key deliverables tied to business goals and objectives. There is significant opportunity for advancement in this role.

ESSENTIAL FUNCTIONS, DUTIES AND RESPONSIBILITIES:

• Provides corporate leadership, strategic vision, and tactical guidance to promote organic growth of the Human Genomics/NGS (Illumina sequencing)-based line of business.
• Guides decisions on appropriate test development utilizing Next Generation Sequencing and other advanced sequencing technologies.
• Responsible for the proper use, interpretation, and execution of clinical guidelines, specifically those related to CAP, CLIA, ISO, and FDA requirements.
• Fulfills duties by thoroughly understanding due diligence, asset valuation, alliance development, and portfolio development in molecular diagnostics.
• Responsible for leading technology assessment efforts, including new, emerging technologies in advanced sequencing/NGS and/or personalized molecular medicine.
• Capable of delivering complex molecular assays and validation documents under tight timelines.
• Complies with applicable regulatory and accrediting agency requirements.
• Writes validation documents that are compliant with CAP, CLIA, ISO, and FDA requirements.
• Understands and follows the Compliance plan.
• Promotes and maintains positive relationships with all contacts.
• Facilitates resolution of conflicts and problems as appropriate
• Promotes effective interpersonal and interdepartmental relationships.
• Adopts a team approach to work and acts as a role model providing leadership.
• Maintains a professional attitude when serving our customers, including patients, physicians, and staff.
• Demonstrates the ability to communicate effectively and cooperate with all contacts.
• Displays patience, tact, a cheerful disposition, and enthusiasm.
• Willing to work beyond normal working hours, shifts, or positions when necessary.
• Complies with all MPLN policies and procedures as stated in the employee handbook.
• Assists directors and managers with job orientation, growth, and development.
• Contributes to innovation and continuous improvement of new ideas and better ways of doing things.

KNOWLEDGE, SKILLS, AND EXPERIENCE REQUIRED:

• The Genomics Scientist should have at least 2 years’ experience developing NGS-based Laboratory-Developed Tests (LDTs) for the CLIA environment.
• Five or more years of experience in esoteric assay development is preferred.
• A history of contributions to NGS guidelines and scholarly publications is highly desirable.

EDUCATION, LICENSE OR CERTIFICATIONS REQUIRED:

• The Genomics Scientist must have earned a doctoral degree from an accredited institution in biological science.
• Significant job experience must be evident, including biochemistry or clinical laboratory science.
• Recent, relevant hands-on experience with NGS library preparation, workflows and bioinformatics is required.
• Applicable clinical licensure (e.g., HCLD) is preferred but not required.

WORK ENVIRONMENT:

The work area is well-lit and well-ventilated. The potential for exposure to communicable diseases, infectious materials, and potentially harmful chemicals is moderate. MPLN provides appropriate safety training to mitigate these risks.

PHYSICAL / MENTAL DEMANDS:

A moderate amount of walking, standing, and bending over at desktop and counter-height work surfaces is expected. Sitting for long periods of time may be required, including extended periods working at a computer or reading printed matter. Manual dexterity with both hands is a key demand for effective operation of laboratory instruments and equipment, and for keyboarding. Moderate exposure to musculoskeletal strain may occur from lifting and carrying packages and from reaching above one’s head to place or retrieve stored items. Hearing and vision (aided if necessary) should be within normal ranges.

Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Some studies will require that operators successfully complete a study-specific qualification protocol that comprises both technical and administrative (organizational) elements; failure to formally ‘qualify’ for a study will preclude participation in those studies.

MPLN is an Equal Opportunity Employer.

Candidates must be able to pass a pre-employment background check and drug test.