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Remote Merck Clinical Trials 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 ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

... trials to bring life-changing therapies to patients in need across the globe. We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

... trials to bring life-changing therapies to patients in need across the globe. We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

... trials to bring life-changing therapies to patients in need across the globe. We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are ...

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All JobsMerck Clinical Trials JobsRemote Merck Clinical Trials JobsRemote Merck Clinical Trials Jobs in Raleigh, NC

Remote Merck Clinical Trials information

See Raleigh, NC salary details

$19

$41

$79

How much do remote merck clinical trials jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for remote merck clinical trials in Raleigh, NC is $41.88, according to ZipRecruiter salary data. Most workers in this role earn between $35.53 and $41.83 per hour, depending on experience, location, and employer.

What is a remote Merck clinical trial?

Remote Merck Clinical Trials are research studies conducted by Merck & Co., Inc. that allow participants to take part from their homes or other locations outside of traditional clinical sites. These trials use digital technologies, such as telemedicine, mobile apps, and wearable devices, to monitor participants, collect data, and communicate with study teams. Remote trials aim to make participation more convenient, increase patient diversity, and improve data collection. They may include virtual visits, home delivery of study medications, and remote monitoring of health outcomes. This approach helps expand access to clinical research while maintaining the safety and integrity of the study.

How do remote team members in Merck clinical trials collaborate with on-site staff and ensure seamless trial operations?

Remote team members in Merck Clinical Trials utilize secure digital platforms for communication, data management, and document sharing to stay connected with on-site colleagues. Regular virtual meetings, clear scheduling, and standardized protocols help bridge the distance and maintain alignment on clinical trial milestones. Collaboration tools such as electronic trial master files (eTMF) and project management software are commonly used to track progress and address challenges promptly. This structure enables remote staff to contribute effectively to trial operations, support patient recruitment, and monitor compliance while maintaining efficiency and strong team integration.

What are the key skills and qualifications needed to thrive as a remote clinical trials specialist at Merck?

To excel as a Remote Clinical Trials Specialist at Merck, you generally need a background in life sciences or healthcare, experience in clinical research, and familiarity with Good Clinical Practice (GCP) guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and sometimes certifications like SOCRA or ACRP are commonly required. Strong organizational skills, attention to detail, and effective remote communication are essential soft skills for managing study protocols and collaborating with diverse teams. These competencies are crucial for ensuring regulatory compliance, data integrity, and the efficient coordination of clinical research activities from a remote setting.

What is the difference between Remote Merck Clinical Trials vs Remote Clinical Research Associate?

AspectRemote Merck Clinical TrialsRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonSame as Merck Clinical Trials, often requiring similar degrees and certifications
Work EnvironmentRemote, often within pharmaceutical or biotech companies like MerckRemote, working on clinical trial sites or for research organizations
Employer & Industry UsagePrimarily employed by pharmaceutical companies like Merck, focusing on clinical trial managementEmployed by CROs or pharmaceutical companies, focusing on site monitoring and trial coordination

Both roles involve clinical trial work with similar credentials and work environments. The main difference is that Remote Merck Clinical Trials refers to roles within Merck's clinical trial programs, while Remote Clinical Research Associates typically work across various organizations, focusing on site monitoring and trial coordination.

What are the most commonly searched types of Merck Clinical Trials jobs in Raleigh, NC?

The most popular types of Merck Clinical Trials jobs in Raleigh, NC are:

What are popular job titles related to Remote Merck Clinical Trials jobs in Raleigh, NC?

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

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

The top searched job categories for Remote Merck Clinical Trials jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Merck Clinical Trials jobs?

Cities near Raleigh, NC with the most Remote Merck Clinical Trials job openings:

Remote Merck Clinical Trials jobs near you
Infographic showing various Remote Merck Clinical Trials job openings in Raleigh, NC as of August 2026, with employment types broken down into 78% Full Time, 9% Part Time, and 13% Contract. Highlights an 100% Remote job distribution, with an average salary of $87,117 per year, or $41.9 per hour.

Clinical Trials Manager- Remote

Adecco

Chapel Hill, NC • Remote

$62 - $64.73/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago

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.