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Decentralized Clinical Trials Manager Jobs in Rincon, GA

MUSC

Certified Medical Assistant

Bluffton, SC

$15.75 - $20.50/hr

... Manager. Under the direct supervision of a Registered Nurse, the Certified Medical Assistant ... decentralized patient-centered approach to patient care and achieve desired outcomes. Assists in ...

MUSC

Certified Medical Assistant

Bluffton, SC · On-site

$15.75 - $20.50/hr

Summary The Certified Medical Assistant reports to the Outpatient Clinic Manager. Under the direct ... support a decentralized patient-centered approach to patient care and achieve desired outcomes.

MUSC

Certified Medical Assistant

Bluffton, SC · On-site

$15.75 - $20.50/hr

... Manager. Under the direct supervision of a Registered Nurse, the Certified Medical Assistant ... decentralized patient-centered approach to patient care and achieve desired outcomes. Assists in ...

MUSC

Certified Medical Assistant

Bluffton, SC · On-site

$15.75 - $20.50/hr

... Manager. Under the direct supervision of a Registered Nurse, the Certified Medical Assistant ... decentralized patient-centered approach to patient care and achieve desired outcomes. Assists in ...

MUSC

Certified Medical Assistant

Bluffton, SC

$15.75 - $20.50/hr

... Manager. Under the direct supervision of a Registered Nurse, the Certified Medical Assistant ... decentralized patient-centered approach to patient care and achieve desired outcomes. Assists in ...

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All JobsDecentralized Clinical Trials JobsDecentralized Clinical Trials Manager JobsDecentralized Clinical Trials Manager Jobs in Rincon, GA

Decentralized Clinical Trials Manager information

See Rincon, GA salary details

$26

$56

$87

How much do decentralized clinical trials manager jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for decentralized clinical trials manager in Rincon, GA is $56.84, according to ZipRecruiter salary data. Most workers in this role earn between $46.11 and $64.04 per hour, depending on experience, location, and employer.

What does a decentralized clinical trials manager do?

A Decentralized Clinical Trials Manager oversees the planning, implementation, and management of clinical trials that use digital technologies to remotely monitor and collect data from participants. This role involves coordinating virtual and hybrid trial operations, ensuring regulatory compliance, and working with various stakeholders, such as investigators, technology vendors, and sponsors. The manager is responsible for ensuring participant safety, data integrity, and efficient execution of decentralized trial processes, often utilizing telemedicine, wearables, and electronic data capture systems.

What are the key skills and qualifications needed to thrive as a decentralized clinical trials manager?

To excel as a Decentralized Clinical Trials Manager, you need expertise in clinical trial operations, regulatory compliance, and project management, often supported by a degree in life sciences or related field. Familiarity with digital health technologies, remote monitoring platforms, and electronic data capture (EDC) systems is crucial, along with certifications like GCP (Good Clinical Practice). Excellent communication, problem-solving, and adaptability help manage cross-functional teams and rapidly changing trial environments. These skills ensure effective coordination, data integrity, and patient engagement in decentralized clinical research.

What are some common challenges faced by a decentralized clinical trials manager, and how can they be addressed?

A Decentralized Clinical Trials Manager often encounters challenges related to coordinating remote sites, ensuring data quality, and maintaining effective communication among dispersed teams and participants. Addressing these issues requires robust digital platforms for data collection, clear standardized procedures, and regular virtual touchpoints with all stakeholders. Building strong relationships with site coordinators and providing thorough training on decentralized protocols also helps mitigate potential barriers and ensures trial integrity.

What is the difference between Decentralized Clinical Trials Manager vs Clinical Trial Coordinator?

AspectDecentralized Clinical Trials ManagerClinical Trial Coordinator
ResponsibilitiesOversees decentralized trial operations, manages remote sites, ensures compliance across multiple locationsAssists with trial logistics, coordinates site activities, and supports data collection
Required CredentialsBachelor's degree in life sciences, clinical research experience, knowledge of decentralized trial technologiesBachelor's degree, clinical research training, familiarity with trial procedures
Work EnvironmentRemote and on-site, collaborating with multiple decentralized sitesPrimarily on-site or office-based at trial sites or research centers
Industry UsageGrowing in decentralized and virtual trial settingsTraditional clinical trial settings

The Decentralized Clinical Trials Manager focuses on managing remote and decentralized trial operations, while the Clinical Trial Coordinator handles day-to-day site activities. Both roles require clinical research knowledge, but the manager's role is broader, overseeing multiple sites and remote technologies.

What job categories do people searching Decentralized Clinical Trials Manager jobs in Rincon, GA look for?

The top searched job categories for Decentralized Clinical Trials Manager jobs in Rincon, GA are:

What cities near Rincon, GA are hiring for Decentralized Clinical Trials Manager jobs?

Cities near Rincon, GA with the most Decentralized Clinical Trials Manager job openings:

Decentralized Clinical Trials Manager jobs near you
Infographic showing various Decentralized Clinical Trials Manager job openings in Rincon, GA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $118,221 per year, or $56.8 per hour.

Clinical Research Coordinator - Clinical Research

CenExel

Savannah, GA • On-site

$25 - $29/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 8 days ago

CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

64th of 120 rated laboratories

Job description

About Us:
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Schedule: Monday - Friday (08:00 AM - 4:30)
Hourly Rate: $25.00 - $29.00/hr (depending on education, experience, and skillset)
Job Summary:
Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Essential Responsibilities and Duties:
  • Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Monitors, and reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes.
  • Assists the CTM in planning, creating processes, trainings and development of staff.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Must have experience and demonstrate mastery of a Clinical Research Coordinator position.
  • High school graduate or equivalent; Bachelors Degree, preferred
  • CCRC certification preferred
  • 2-3 years of experience in the medical field, preferred
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

Working Conditions
  1. Indoor, Office environment.
  2. Shift work, depending on location.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Overnight travel may be required for training and/or investigative meetings.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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