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Associate Clinical Trial Manager Jobs in Ridgeland, MS

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

Assists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding source * Maintains inventory of study ...

Research Assistant - Wichita, KS

Flowood, MS · On-site

$16.25 - $22.25/hr

... Clinical Trial Management System (CTMS) to ensure proper billing of study procedures to the appropriate funding source. * Collect and report ongoing patient recruitment and enrollment progress and ...

Research Assistant - Flowood, MS

Flowood, MS · On-site

$16.25 - $22.25/hr

Assists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding source * Maintains inventory of study ...

Research Assistant - Wichita, KS

Flowood, MS · On-site

$16.25 - $22.25/hr

... Clinical Trial Management System (CTMS) to ensure proper billing of study procedures to the appropriate funding source. * Collect and report ongoing patient recruitment and enrollment progress and ...

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Associate Clinical Trial Manager information

See Ridgeland, MS salary details

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$33

$58

How much do associate clinical trial manager jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for associate clinical trial manager in Ridgeland, MS is $33.31, according to ZipRecruiter salary data. Most workers in this role earn between $26.83 and $36.63 per hour, depending on experience, location, and employer.

What does an associate clinical trial manager do?

An Associate Clinical Trial Manager assists in the planning, execution, and management of clinical trials to ensure they are conducted in accordance with regulatory guidelines and company protocols. They support the Clinical Trial Manager by coordinating study timelines, managing vendors and sites, and overseeing documentation and reporting. This role involves collaborating with cross-functional teams, identifying and resolving issues, and ensuring that trials meet quality and compliance standards. Associate Clinical Trial Managers play a key part in bringing new treatments to market efficiently and safely.

What are the key skills and qualifications needed to thrive as an associate clinical trial manager?

To thrive as an Associate Clinical Trial Manager, you need a solid understanding of clinical trial processes, regulatory guidelines, and a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for managing timelines and collaborating with multiple stakeholders. These skills and qualifications ensure clinical trials run smoothly, comply with regulations, and deliver reliable results.

What are some common challenges faced by associate clinical trial managers when coordinating cross-functional teams?

Associate Clinical Trial Managers often encounter challenges related to aligning objectives and communication among cross-functional teams, such as regulatory, clinical operations, data management, and vendors. Managing timelines, ensuring all parties are updated on protocol changes, and resolving conflicts between departments can be complex, especially in a fast-paced environment. Proactive communication, attention to detail, and strong organizational skills are essential for overcoming these challenges and maintaining trial quality and compliance.

What is the difference between Associate Clinical Trial Manager vs Clinical Trial Coordinator?

AspectAssociate Clinical Trial ManagerClinical Trial Coordinator
ResponsibilitiesOversees trial operations, manages teams, ensures compliance, and supports trial planningCoordinates trial activities, manages documentation, schedules visits, and assists with data collection
Required CredentialsBachelor's degree, experience in clinical trials, knowledge of GCPBachelor's degree, experience in clinical settings, familiarity with trial procedures
Work EnvironmentTypically in clinical research settings, working closely with managers and teamsOften in clinical sites or research offices, supporting trial staff

The Associate Clinical Trial Manager and Clinical Trial Coordinator roles share similar educational backgrounds and work environments. However, the Associate Clinical Trial Manager has broader responsibilities, including overseeing trial operations and managing teams, while the Clinical Trial Coordinator focuses on day-to-day coordination and documentation tasks. Both roles are essential in clinical research, with the manager position having a higher level of oversight and strategic involvement.

How much does an Associate Clinical Trial Manager earn?

An Associate Clinical Trial Manager typically earns between $70,000 and $100,000 annually, depending on experience, location, and the size of the organization. Entry-level positions may start lower, while experienced managers with certifications can earn higher salaries. Compensation often includes benefits such as health insurance and performance bonuses.

How to become an Associate Clinical Trial Manager?

To become an Associate Clinical Trial Manager, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project coordination. Gaining knowledge of Good Clinical Practice (GCP) guidelines and clinical trial management systems is beneficial. Some roles may require certification such as the Certified Clinical Research Professional (CCRP) or similar credentials.

What job categories do people searching Associate Clinical Trial Manager jobs in Ridgeland, MS look for?

The top searched job categories for Associate Clinical Trial Manager jobs in Ridgeland, MS are:

Registered Dietitian Clinical Research - PRN

Professional Case Management

Jackson, MS • Remote

$42/hr

Part-time

Posted yesterday

New


Professional Case Management rating

5.0

Company rating: 5.0 out of 10

Based on 10 frontline employees who took The Breakroom Quiz


Job description

Make a Difference on Your Own Schedule and Terms!

Hiring Per Diem Registered Dietitians for Virtual Visits!
EmVenio Research provides quality, in-home clinical trial visits for various Sponsors and CROs. We're the only company that hires, trains, certifies, tests, and manages our own Registered Dietitians. Our mission is to bring clinical trial visits to subjects wherever they may be to increase convenience and compliance with study protocols.
Be part of a team who fully embrace our values and key behaviors!

  • We work as a team
  • We do the right thing
  • We figure it out
  • We pursue growth
  • We take ownership

Why work for EmVenio?

  • We bring research to every neighborhood - making it more accessible, more inclusive, and more human - so every community can share in the promise of better care.
  • Be a member of our general staffing pool
  • No research experience required, on the job training provided
  • Gain Certification through GCP training

Required Qualifications

  • Bachelor's degree from an accredited dietetics program (If CDR examination was before January 1, 2024)
  • Graduate degree from an accredited dietetics program (If CDR examination was on or after January 1, 2024)
  • Registered Dietitian (RD) or Registered Dietitian Nutritionist (RDN) Certification by the Commission on Dietetic Registration (CDR)
  • Current State Dietitian License/Certification in good standing (if applicable)

Job Specific Details:

  • Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values.
  • Sets appointments with subjects within the required appointment window.
  • Completes virtual visits for clinical trial subjects.
  • Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner.
  • Regularly stay informed on the latest nutrition and food health updates.
  • Performs additional duties and responsibilities as deemed necessary.
Standard Rate: $42.00 Hourly plus commute, mileage, training, and administrative pay.Please contact Brandi Johnson at (303) 764-4289 or at brandi.johnson@emvenio.com today to learn more about our opportunities where you can make a difference in your own career!

Professional Case Management is an Equal Opportunity Employer.


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About Professional Case Management

Sourced by ZipRecruiter

Since 1997, Professional Case Management (PCM) has been providing quality, nationwide in-home nursing services to sufferers of chronic diseases. We are the nation's premier healthcare provider for nuclear weapons workers, uranium miners, millers and haulers suffering from illnesses contracted in the course of their employment. Our mission is to deliver quality care to enhance patient outcomes in the privacy and comfort of their homes.

Industry

Health care and social assistance

Company size

201 - 500 Employees

Headquarters location

Denver, CO, US

Year founded

1986

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