Data Coordinator

Job Description

Data Coordinator:
On behalf of our Clinical Research client, Procom is searching for a Data Coordinator for a 1-year role. This position is a fully onsite position at our client’s Chapel Hill, NC office.

Job Description:
The Data Coordinator supports oncology clinical research by managing data-related activities throughout the clinical trial lifecycle. This role involves ensuring the accurate collection, abstraction, review, and submission of clinical trial data, working closely with study coordinators, investigators, and clinical teams to maintain data integrity and support protocol compliance.

Responsibilities:
• Abstract clinical information from medical records and source documents according to study-specific requirements.
• Collect, review, and enter clinical trial data into electronic data capture systems and case report forms.
• Ensure data accuracy, completeness, and timely submission.
• Resolve data queries within sponsor-required timelines.
• Maintain research patient records and study documentation.
• Track serious adverse events and associated follow-up information.
• Collaborate with regulatory staff and study teams to ensure protocol adherence.
• Participate in study startup, initiation, monitoring, and closeout meetings.

Mandatory Skills:
• Bachelor's degree or an equivalent combination of education and experience.
• Experience with data entry, documentation, and quality control.
• Ability to manage multiple research studies simultaneously while meeting strict deadlines.
• Strong computer proficiency and database management skills.
• Excellent written and verbal communication skills.
• Strong organizational skills and attention to detail.
• Ability to work effectively in a collaborative team environment.

Nice-to-Have Skills:
• At least one year of Data Coordinator experience or equivalent oncology clinical research experience.
• Experience supporting therapeutic clinical trials involving investigational drugs and/or medical devices.
• Experience with Phase I, II, or III clinical trials.
• Experience working with Clinical Trial Management Systems such as OnCore.
• Knowledge of ICH-GCP guidelines, federal regulations, and protocol-driven research.

Assignment Length:
This is a 1-year contract position.

Start Date:
ASAP.

Assignment Location:
Chapel Hill, NC, fully onsite.