Clinical Research Associate-Early Drug Development

Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education.

https://youtu.be/9R7QoNfmm0w

We have an exciting opportunity in our Early Drug Development 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 portfolio for a Service and/or Department.

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 stakeholders, and identify study trends and create/implement solutions.
• Perform diverse research-related functions using sound judgment and exceptional organizational skills.

You are:

• Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders.
• 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 stakeholder needs.

You have:

• HS Diploma/GED with 2-4 years relevant 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.