Clinical Research Coordinator — Hybrid, Part-Time

Amaris Consulting; McComb (MS); Hybrid; USD 65,000 - 90,000; Part time

Job summary

Amaris Consulting is seeking an experienced Research Coordinator in McComb, MS, to manage day-to-day clinical study activities at the site. The RC will liaise between investigators, sponsor, and site staff, ensuring protocol adherence, GCP, and regulatory requirements are met.

The role supports enrollment, data management, and sponsor visits in a part-time, hybrid on-site setting. The ideal candidate has a Bachelor's degree in a related field plus 5 years of clinical research coordination

Qualifications

• Bachelor's degree in a related field required.
• 5 years of Clinical Research Coordination experience required.
• Experience conducting sponsored research studies required.
• Strong understanding of ICH-GCP guidelines, FDA regulations, and IRB submissions.
• Experience with Electronic Data Capture (EDC) systems and Medidata Rave.
• Ability and willingness to travel on-site to support study activities.
• Strong organizational and communication skills.
• Experience in subject enrollment management, source documentation, data entry, adverse event reporting, site regulatory documentation, and query resolution.

Responsibilities

• Coordinate patient enrollment activities.
• Collect, review, and maintain source documentation and study records.
• Enter study data into EDC systems and resolve data queries.
• Maintain regulatory binders and essential study documentation.
• Prepare for and support sponsor monitoring visits, audits, and site inspections.
• Ensure participant safety, confidentiality, and protocol compliance throughout the study.
• Collaborate with investigators, radiology staff, and study teams to ensure protocol-required procedures are completed.

Skills

Clinical Research Coordination

GCP knowledge

Regulatory knowledge

Communication

Project coordination

On-site travel

Education

Bachelor's degree in a related field

Tools

EDC systems

Medidata Rave

Job description

Amaris Consulting is seeking an experienced Research Coordinator in McComb, MS, to manage day-to-day clinical study activities at the site. The RC will liaise between investigators, sponsor, and site staff, ensuring protocol adherence, GCP, and regulatory requirements are met.

The role supports enrollment, data management, and sponsor visits in a part-time, hybrid on-site setting. The ideal candidate has a Bachelor's degree in a related field plus 5 years of clinical research coordination