Clinical Research Associate-Program for Drug Development- Leukemia Service

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 Clinical Research Associate Program for Drug Development Leukemia Service for 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 oordinates 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.