Clinical Research Coordinator

Amaris Consulting; McComb (MS); Hybrid; USD 55,000 - 69,000; Part time

Job summary

Amaris Consulting is seeking a Clinical Research Coordinator to manage day-to-day study operations at an investigative site in McComb, MS. The role is hybrid, part-time (2–3 days/week), with a 4-month contract and a pay rate of $40–$50 per hour.

You will ensure protocol compliance, data integrity in EDC, and close collaboration with investigators and sponsor teams. The ideal candidate holds a Bachelor's degree, has 5 years of CRC experience, and is proficient with EDC systems and Medidata Rave.

Qualifications

• 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.

Responsibilities

• 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 closely with investigators, radiology staff, and study teams to ensure protocol-required procedures are completed.

Skills

Clinical Research Coordination

GCP & FDA regulations

Communication

Travel readiness

Education

Bachelor's degree in a related field

Tools

Medidata Rave

Job description

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.