Note: The job is a remote job and is open to candidates in USA. Moffitt Cancer Center is a National Cancer Institute-designated Comprehensive Cancer Center focused on the prevention and cure of cancer. The Associate Clinical Research Coordinator supports clinical trial data collection and coordination, including participant consent, specimen collection, data entry, patient follow-up, regulatory documentation, and communication with study sponsors.
Responsibilities
- The Clinical Research Coordinator Associate is a support position that administers duties related to the collection of data and/or the coordination of clinical trials, at Moffitt Cancer Center. Activities support assigned research protocols and include the coordination activities of assigned research protocols (generally non-therapeutic in nature) including obtaining informed consent from study participants, specimen collection and data entry
- The job is a pre-entry position for the Clinical Trials Coordinator career path or other medical or research career paths
- Other job duties may include support of therapeutic studies including completion of data entry into various database systems, follow-up of patients according to protocol (via review of records, clinic visit or telephone call), ordering supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, communicating with study sponsors, and facilitating the collection of study-required specimens
- The position applies job skills and company policies and procedures to complete assigned tasks. Within its administrative support duties, it receives moderate supervision. The assignments are semi-routine in nature, but the CRC Associate recognizes the need for occasional deviation from accepted practice. Requires instructions only on new assignments
Skills
- Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills
- Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences
- Familiarity with regulatory requirements in clinical research or ability to successfully learn this
- Experience interacting with patients and coordinating care with medical staff
- Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol
- Associate's degree
- In lieu of an associate's degree, 2 years of relevant experience required with a high school diploma or GED
- Prior experience in clinical trials is preferred
- Bachelor's degree preferred in scientific, health related or business administration program
Benefits
- Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.
- Paid training and orientation through its CTO (Clinical Trails Office) Academy.
- Relocation assistance may be provided.
Company Overview
Company H1B Sponsorship