Clinical Research Coordinator

We are looking for an Clinical Research Coordinator to support the day-to-day management and execution of a clinical research study at an investigative site. You will serve as the primary liaison between investigators, sponsor, and site staff, ensuring the study is conducted in compliance with the protocol, Good Clinical Practice (GCP), regulatory requirements, and institutional policies. Key Information: Location: McComb , Mississippi, USA Work Mode: hybrid This is a part-time role requiring 2–3 days of work per week . Length of contract: 4 months Type of contract: C2C Salary rate: 40-50 USD per hour Key Tasks: Collect, review, and maintain source documentation and study records Enter study data into Electronic Data Capture (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 closely with investigators, radiology staff, and study teams to ensure protocol-required procedures are completed Profile Must-Haves: Bachelor's degree in a related field 5 years of Clinical Research Coordination experience Experience conducting sponsored research studies Strong understanding of ICH-GCP guidelines, FDA regulations, and IRB submissions Experience with Electronic Data Capture (EDC) systems Experience with 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 Nice-to-Haves: Experience in an imaging environment (particularly CT) to support imaging-related study activities Why choose us An international community bringing together more than 110 different nationalities An environment where trust is central: 70% of our leaders started their careers at the entry level A strong training system with our internal Academy and more than 250 modules available A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.) Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics. #J-18808-Ljbffr