Temp Oncology Study Coordinator (Onsite)

NC State University; Raleigh (NC); On-site; USD 37,000 - 53,000; Part time

Benefits offered by this job

Health insurance for temporary-emps

LEAD courses

Attend sporting events for free

Childcare discounts

Wellness membership

Wellness programs

Job summary

NC State University in Chapel Hill, NC is seeking a UTS - Temporary Study Coordinator to oversee oncology clinical trials from startup through closeout. The role involves coordinating activations, enrollments, monitoring, and regulatory documentation on-site with UNC Medical Center and affiliated clinics.

You will work with investigators, sponsors, and study teams to ensure adherence to protocol, GCP, and FDA regulations, while coordinating patient visits, informed consent, and data entry in

Qualifications

• Bachelor’s degree in related scientific, healthcare, or research discipline.
• At least one year of relevant research experience.
• Experience with oncology clinical trials preferred.

Responsibilities

• Coordinate oncology clinical trials from startup through closeout.
• Maintain study documentation and regulatory records.
• Ensure GCP, FDA regulations compliance.
• Interact with investigators, sponsors, and clinical teams.
• Coordinate patient visits and informed consent.

Skills

Oncology research

Study coordination

GCP knowledge

Education

Bachelor's degree

Tools

Epic/EMR

Job description

NC State University in Chapel Hill, NC is seeking a UTS - Temporary Study Coordinator to oversee oncology clinical trials from startup through closeout. The role involves coordinating activations, enrollments, monitoring, and regulatory documentation on-site with UNC Medical Center and affiliated clinics.

You will work with investigators, sponsors, and study teams to ensure adherence to protocol, GCP, and FDA regulations, while coordinating patient visits, informed consent, and data entry in