Director, Research & Development

Director, Research & Development

Eurofins Transplant Genomics Inc. ("ETG") is a molecular diagnostics company committed to improving organ transplant outcomes with non-invasive serial monitoring guided by biomarkers. ETG's product portfolio of both individual and combined whole blood gene expression and donor derived cell-free DNA testing is capable of reliably ruling out subclinical kidney rejection and acute rejection in kidney transplant patients. In addition to kidney transplantation testing, our newest product for liver transplant patients is a blood-based biomarker assay designed to rule out rejection as immunosuppression therapy is optimized.

Basic Function and Scope of Responsibility :

The Research and Development Director is primarily responsible for the leadership, development, optimization and validation of innovative methods in transplant diagnostics by utilizing technologies based on molecular, proteomic and / or bioinformatics approaches.

Qualifications

• Advanced degree in microbiology, immunology, biology, biochemistry or a related field is required; PhD required
• At least 3 years of experience in assay development, validation and transition to a clinical environment required
• Minimum of 3 years of management or team / program leadership experience required.
• Demonstrated proven experience in managing complex projects, ability to succeed even with challenging projects, appreciation of priorities and critical factors.
• Expertise and experience in biochemistry, molecular biology / genomics, or immunology assay development, verifiable through patents, publication or description of completed projects required
• Extensive experience and demonstrated accomplishments in diagnostic testing and related fields with an emphasis on advanced, innovative and industry-leading approaches.
• A strong understanding and background in laboratory medicine, especially diagnostics used to guide clinical actions, such as treatments, the choice of drugs or drug combinations
• Working knowledge of clinical laboratory regulatory topics (CLIA, CAP, NYDOH)
• Substantial technical writing experience : protocols, study reports, regulatory communications and manuscripts
• An innovative and prepared mind to identify and protect unique intellectual properties is a bonus
• Commitment to and track record of high quality of work
• Ability to establish and maintain effective working relationships with other groups
• Goal oriented, with excellent time management and organizational skills
• Excellent interpersonal skills, with ability to interact effectively and work efficiently with people at all levels in an organization
• Excellent verbal & written communication skills

Additional Information

Schedule : Monday - Friday, 8 am - 5 pm + travel

Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.