Building Location:Building A - Duluth Clinic - 1st Street

Department:49973 Oncology Clinical Trials

Job Description:Provides expertise and assistance in the conduct of clinical trials. As the resource for the protocols, will serve as a liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor. Prepares reports and tables used to disseminate current information for management decisions. Facilitates on-going communication and efficient operation of research activity and ensures the expeditious retrieval of information. The Specialist is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.

Education Qualifications:

Bachelor’s degree plus 2 years’ experience in a research environment OR Extensive course work in business
OR

Health administration and 4 years’ experience in research and/or regulatory environment, including protocol management and customer relations.
 

Licensure/Certification Qualifications:

SOCRA (Society of Clinical Research Associates) or ACRP (Associate of Clinical Research Professionals) certification, or ability to obtain within three years of hire date.

FTE:1

Possible Remote/Hybrid Option:

Shift Rotation:Day Rotation (United States of America)

Shift Start Time:0800

Shift End Time:1700

Weekends:

Holidays:No

Call Obligation:No

Union:

Union Posting Deadline:09/11/2024 11pm