Consider an outstanding opportunity to be at the forefront of supporting Memorial Sloan Kettering Cancer Center's renowned leadership. We have an exciting opportunity in our Compliance Service as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA) coordinates and maintains the assigned research portfolios for a Service and/or Department.

Memorial Sloan Kettering physicians conduct one of the worlds largest clinical cancer research programs. Investigators from various fields and departments join efforts to improve the prevention, The faculty and staff of Memorial Sloan Ketterings clinical departments and divisions possess an unparalleled depth and breadth of clinical expertise. Our outstanding scientists and clinicians work together to drive innovation and seek some of the greatest challenges of biomedical science.

You Will:

• Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols.
• Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight.
• Effectively communicate the overall study progress to various internal and/or external partners, and identify study trends and build/implement solutions.
• Perform diverse research-related functions using sound judgment and exceptional interpersonal skills.

You are:

• Adept at anticipating and prioritizing work to meet commitments of multiple partners.
• Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals.
• Known as someone who improves processes and proactively, independently identifies solutions that anticipate partner needs.

You have:

• HS Diploma/GED with 2-4 years meaningful work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelors Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory.
• Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required.
• Proficiency with the Electronic Medical Record (EMR) system.
• Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics.
• Knowledge of clinical research data collection processes in accordance with GCP.