Research Associate III
About The Position
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 assisting the research team with recruitment activities, administering questionnaires. Contributes to the development of research protocols and understanding research design including assists with database enhancements.
Requirements
- Bachelor Degree required - Bachelor's degree in life science or public health.
- 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 a variety of concepts, practices and procedures in a directly related field.
Nice To Haves
- Masters Degree preferred.
- Medical Degree (or foreign equivalent), Preferred.
- ACRP (or SOCRA) certification required within 18 months of employment.
Responsibilities
- Supports the research team in the overall conduct of clinical trials using Good Clinical Practice.
- Functions independently and leads the Research Associate for the disease group, including mentoring, training, and reviewing/auditing data accuracy of junior Research Associates.
- Ensures timely collection of protocol data and samples, including shipment to outside entities.
- Obtains informed consent for 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 such as assisting with recruitment and administering questionnaires.
- Contributes to the development of research protocols and understanding research design.
- Assists with database enhancements.
Benefits
- An assortment of insurance products and discount programs through Voluntary Benefits.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
