Clinical Research Coordinator: Learn & Lead Trials

Good Samaritan Society; Fargo (ND); On-site; USD 33,000 - 53,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

401(k) retirement plan

Work/life balance benefits

Generous time off

Job summary

Sanford Health in Fargo, ND is hiring a Clinical Research Coordinator to learn daily and contribute to future treatments through coordinating tests, procedures, and investigational treatments in various clinical trials.

The role involves educating staff about the research process, scheduling site visits, tracking enrollment goals, and ensuring proper documentation and regulatory compliance. Local travel may be required.

Qualifications

• Bachelor's degree in biology, microbiology or related field.
• Minimum three years of clinical or clinical research experience or six to eight years of relevant work experience.
• If an LPN, currently holds an unencumbered LPN license with state nursing board and/or possess multi-state licensure privileges.

Responsibilities

• Coordinate tests, procedures, and investigational treatments for various conditions and symptoms.
• Schedule and coordinate pre-study site visits and monitor enrollment goals.
• Maintain patient screening/enrollment logs and update sponsors/CROs/SMOs.
• Ensure completion of screening, eligibility and enrollment procedures.
• Conduct interviews to assess subject ability and willingness to follow procedures.
• Prepare case report forms and ensure data accuracy and source documentation.
• Schedule sponsor monitoring visits and audits for regulatory compliance.
• Occasional local travel between sites and supervise students.

Skills

Clinical research experience

Education

Bachelors degree in biology, microbiology or related field

Licensed Practical Nurse (LPN) license (if applicable)

Job description

Sanford Health in Fargo, ND is hiring a Clinical Research Coordinator to learn daily and contribute to future treatments through coordinating tests, procedures, and investigational treatments in various clinical trials.

The role involves educating staff about the research process, scheduling site visits, tracking enrollment goals, and ensuring proper documentation and regulatory compliance. Local travel may be required.