Clinical Research Lab Manager – IRB & NIH Trials

Clemson University; Seneca (SC); On-site; USD 58,000 - 65,000; Full time

Job summary

Clemson University is seeking a temporary grant staff member to support NIH-funded research projects at the Clemson site. The role includes supervising staff, ensuring protocol adherence, and overseeing regulatory compliance across sites in Greenville and Seneca, SC.

Responsibilities include data collection, charting study timelines, and preparing deliverables while coordinating with the PI. A Bachelor of Science in a related field and clinical lab experience are required.

Qualifications

• Bachelor degree in a relevant science field and clinical/research lab experience.
• Experience with phlebotomy is preferred.

Responsibilities

• Recruit, train, coordinate and supervise staff to implement study policies and ensure data quality.
• Oversee protocol implementation, IRB approvals, regulatory documents and meetings.
• Monitor compliance with regulations and ensure proper document/version control.
• Manage study communications, meetings and preparation of study documents.
• Prepare presentations and assist with publications and funder reports.

Skills

NIH-funded studies / clinical trials

Older adults / diverse populations

REDCap

Qualtrics

Education

Bachelor of Science in medical technology, microbiology, biochemistry or closely related field

Tools

REDCap

Qualtrics

Job description

Clemson University is seeking a temporary grant staff member to support NIH-funded research projects at the Clemson site. The role includes supervising staff, ensuring protocol adherence, and overseeing regulatory compliance across sites in Greenville and Seneca, SC.

Responsibilities include data collection, charting study timelines, and preparing deliverables while coordinating with the PI. A Bachelor of Science in a related field and clinical lab experience are required.