Translational Research Administrator

New York University • New York, NY

1d • $70,000 - $84,150

About The Position

The Translational Research Administrator (TRA) is a crucial link between basic scientific research and clinical application, involving the management and facilitation of research projects aimed at translating laboratory findings into potential therapies, diagnostics, and treatments for patients. Provide support to the Director of Clinical Research Operations in clinical trial protocol development, budgeting, Institutional Review Board (IRB) applications, subject recruitment and consenting. Manage the planning, collection and initial processing of tissue and bodily fluids for research projects as well as research subject data. Develop and manage Standard Operating Procedures and databases. Prepare and submit regular progress reports to funding agencies as required by each study. Provide support to the senior clinical research staff and administration to ensure compliance with Federal and Institutional Policy, the Institutional Review Boards (IRB) Good Clinical Practice (GCP), and all other governance requirements.

Requirements

• Bachelor's Degree
• 3+ years relevant experience in translational research or equivalent combination of education and experience.
• Must include research database development experience.
• Strong understanding of regulatory requirements and ethical considerations in translational research.
• Excellent project management and organizational skills.
• Proficiency in Microsoft Office Suite, project management software, and data analysis tools including RedCap and LabVantage.
• Strong communication and interpersonal skills, with the ability to work collaboratively in a multidisciplinary team environment.

Nice To Haves

• Master's Degree in a biomedical science-related field (e.g., molecular biology, pharmacology, clinical research, biomaterials).

Responsibilities

• Provide support to the Director of Clinical Research Operations in clinical trial protocol development, budgeting, Institutional Review Board (IRB) applications, subject recruitment and consenting.
• Manage the planning, collection and initial processing of tissue and bodily fluids for research projects as well as research subject data.
• Develop and manage Standard Operating Procedures and databases.
• Prepare and submit regular progress reports to funding agencies as required by each study.
• Provide support to the senior clinical research staff and administration to ensure compliance with Federal and Institutional Policy, the Institutional Review Boards (IRB) Good Clinical Practice (GCP), and all other governance requirements.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level