Research Coordinator (Clinical Research)

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

Job Description We are looking for an experienced Research Coordinator (RC) to support the day-to-day management and execution of a clinical research study at an investigative site. The coordinator 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: Part-time / hybrid on-site

Key Tasks

• Coordinate patient enrollment activities
• 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

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.

Who are we?

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We're focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:

Brief Call: Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!

Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!

Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.

As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.

We look forward to meeting you!