The Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate is able to function independently and is the lead Research Associate for the disease group which includes mentoring, training and reviewing/auditing accuracy of data of the junior Research Associates.  The Senior Research Associate ensures timely   collection of protocol data and samples including shipment to outside entities as required. This individual obtains informed consent of non-interventional studies, collects, maintains and organizes study information including compilation, registration and submission of data, as required by the Sponsor. Attends clinic as needed to perform activities including but not limited to assist the research team with recruitment activities, administer questionnaires. Contributes to the development of research protocols and understanding research design including assists with database enhancements.

Bachelor Degree required - Bachelor's degree in life science or public health, preferred

Masters Degree preferred

Medical Degree (or foreign equivalent), Preferred

ACRP (or SOCRA) certification required within 18 months of employment

3 years of work experience required

GCP training required

MS Office proficient.

Life Sciences or Public Health background preferred.

Excellent written and oral communication skills

Exceptional attention to detail and accuracy

Ability to manage multiple tasks & priorities

Demonstrated leadership potential

Knowledge of variety of concepts, practices and procedures in directly related field