In this position you are responsible for regulatory activities within the research department that require an in-depth understanding of Federal, Sponsor, and Institutional Review Board (IRB) regulatory guidelines. Ensures all cancer research protocols are administered meeting regulatory and legal requirements. Functions as first contact person for questions and audits related to regulatory aspects of the cancer research program including audits by the Federal Government, Sponsor(s) and internal. Supports and implements patient safety and other safety practices as appropriate. Supports and demonstrates Family Centered Care principles when interacting with patients and their families and with co-workers.

Schedule

Full-Time | Options for 64 or 72 hours per two weeks | Onsite Days | Monday-Friday | 8am-4:30pm No weekends or holidays!

Pay and Benefits

$20.45 or more per hour, pay determined by experience. Full-time benefits: medical, dental, PTO, retirement, employee discounts and more! Tuition reimbursement and college grant programs available. 

Qualifications

Associate degree or higher degree required or two years' experience in a science, research, health related or complex administrative setting required. Clinical Research Associate National Certification preferred. Training and knowledge of clinical research activities and regulatory requirements. 2 years Minimum of experience in clinical trial conduct preferred. Working understanding of medical terminology and the ability to communicate with staff and leadership. Strong organizational skills in addition to the ability to multitask and prioritize required.

CentraCare has made a commitment to diversity in its workforce. All individuals including, but not limited to, individuals with disabilities, are encouraged to apply. CentraCare is an EEO/AA employer.