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Decentralized Clinical Trials Manager Jobs in Raleigh, NC

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

Clinical Trials Manager (CTM) Location: Remote Schedule: Full-Time | Eastern Time Zone Hours Pay: $62.00-$64.73 per hour Position Overview We are seeking an experienced Clinical Trials Manager (CTM ...

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Significant experience in clinical research, decentralized clinical trials, clinical operations, project management, patient/site services, or related healthcare services. * Experience supporting ...

IQVIA

Director, Remote Research Clinicians

Durham, NC · Remote

Significant experience in clinical research, decentralized clinical trials, clinical operations, project management, patient/site services, or related healthcare services. * Experience supporting ...

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All JobsDecentralized Clinical Trials JobsDecentralized Clinical Trials Manager JobsDecentralized Clinical Trials Manager Jobs in Raleigh, NC

Decentralized Clinical Trials Manager information

See Raleigh, NC salary details

$28

$60

$93

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

As of Sep 8, 2026, the average hourly pay for decentralized clinical trials manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 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 are popular job titles related to Decentralized Clinical Trials Manager jobs in Raleigh, NC?

For Decentralized Clinical Trials Manager jobs in Raleigh, NC, the most frequently searched job titles are:

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

The top searched job categories for Decentralized Clinical Trials Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Decentralized Clinical Trials Manager jobs?

Cities near Raleigh, NC 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 Raleigh, NC 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 $126,404 per year, or $60.8 per hour.

Clinical Trials Manager- Remote

Adecco

Chapel Hill, NC • Remote

$62 - $64.73/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Key responsibilities

  • Manage clinical operational and quality activities for assigned studies in compliance with ICH/GCP and applicable regulations.

  • Develop and maintain clinical tools, monitoring plans, guidelines, and study documentation.

  • Monitor clinical timelines, metrics, site performance, and study progress.

Job description

Clinical Trials Manager (CTM)

Location: Remote
Schedule: Full-Time | Eastern Time Zone Hours
Pay: $62.00–$64.73 per hour

Position Overview

We are seeking an experienced Clinical Trials Manager (CTM) to oversee the clinical operational and quality aspects of assigned clinical studies. This role is responsible for ensuring clinical deliverables are completed on time, within scope, and to quality standards, while supporting patient recruitment, study performance, and overall trial execution.

The ideal candidate will have strong clinical operations experience, excellent leadership and organizational skills, and a solid understanding of ICH/GCP, FDA regulations, clinical monitoring, and patient recruitment strategies.

Key Responsibilities

  • Manage clinical operational and quality activities for assigned studies in compliance with ICH/GCP and applicable regulations.

  • Develop and maintain clinical tools, monitoring plans, guidelines, and study documentation.

  • Support development and maintenance of the Trial Master File (TMF) and ensure document quality and completeness.

  • Collaborate with Project Managers, clinical teams, data management, and other departments to meet study deliverables.

  • Lead clinical team meetings and ensure timelines, resources, communication, and quality objectives are maintained.

  • Monitor clinical timelines, metrics, site performance, and study progress.

  • Review monitoring reports, oversee CRF collection and query resolution, and implement recovery actions when needed.

  • Support patient recruitment strategies and work with study sites to address recruitment and retention challenges.

  • Communicate with study sites regarding protocol requirements, patient participation, CRFs, and study-related issues.

  • Coordinate study start-up activities and support timely ethics committee and regulatory submissions.

  • Ensure essential documents meet regulatory and quality requirements.

  • Support clinical resource planning, delegation of responsibilities, and identification of additional staffing needs.

  • Provide regular project status updates and contribute to client meetings and presentations.

  • Support forecasting, budgeting, and management of clinical project resources.

  • Ensure timely archiving of study documents and materials.

Qualifications

  • Bachelor's degree or equivalent relevant education.

  • 5+ years of relevant clinical research/clinical operations experience or comparable experience.

  • Strong understanding of ICH/GCP, FDA guidelines, and clinical trial requirements.

  • Experience with clinical monitoring practices and study operations.

  • Demonstrated experience with patient recruitment and retention strategies.

  • Strong leadership, mentoring, and team-building skills.

  • Excellent planning, organization, and prioritization abilities.

  • Strong problem-solving, judgment, and decision-making skills.

  • Ability to work effectively in a multicultural, matrixed, and changing environment.

  • Strong written and verbal communication skills.

  • Excellent attention to detail and ability to manage multiple priorities.

  • Working knowledge of Outlook, Excel, Word, and clinical research systems.

  • Understanding of budgeting, forecasting, resource allocation, and financial management preferred.

Work Arrangement

  • 100% Remote

  • Must be available to work Eastern Time Zone hours.

  • Full-time position.

Pay Rate: $62.00–$64.73/hour


Pay Details: $62.00 to $64.73 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.