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Remote Clinical Trial Jobs (NOW HIRING)

CPC

Drug Supply/Clinical Trial Supply Manager

Aurora, CO · Remote

$70K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Drug Supply/Clinical Trial Supply Manager to join our team! Responsible for ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Summary The Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

CPC

Drug Supply / Clinical Trial Supply Manager

Aurora, CO · Remote

$70K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are looking for a Drug Supply/Clinical Trial Supply Manager to join our team! Responsible for ... Flexible and remote work schedules An Equal Opportunity Employer CPC provides equal employment ...

ICON

Clinical Development Trial Lead

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Development Trial Lead ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

ICON

Sr. Clinical Trial Manager

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... clinical teams and sites, as applicable. * If applicable, region specific deliverables will be specified. * Autonomy with execution of local trial management services. * Depth of knowledge with local ...

IQVIA

Clinical Trial Psych Rater

Colton, CA · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

IQVIA

Clinical Trial Psych Rater

Carlsbad, CA · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

IQVIA

Clinical Trial Psych Rater

Gilbert, AZ · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

IQVIA

Clinical Trial Psych Rater

Scottsdale, AZ · Remote

Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

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Remote Clinical Trial information

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How much do remote clinical trial jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for remote clinical trial in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is a remote clinical trial?

A Remote Clinical Trial job involves managing or supporting clinical research studies from a remote location rather than on-site at a hospital or research facility. Responsibilities may include data management, patient monitoring, regulatory compliance, and coordinating trial activities. These roles are often held by clinical research associates, coordinators, or data analysts who use digital tools to oversee the trial process. Remote roles help improve accessibility and efficiency while maintaining compliance with regulatory standards.

What are the key skills and qualifications needed to thrive in a remote clinical trial role?

To thrive in a Remote Clinical Trial position, you need a strong background in clinical research, regulatory compliance, and data management—often supported by a degree in life sciences or health-related fields. Familiarity with electronic data capture (EDC) systems, clinical trial management software (CTMS), and certifications like GCP (Good Clinical Practice) are highly beneficial. Exceptional organizational skills, attention to detail, and proactive communication are essential soft skills for remote collaboration and project management. These abilities ensure accurate trial execution, compliance with protocols, and seamless teamwork across distributed environments.

What are some common challenges faced in remote clinical trial roles, and how can they be managed?

One of the main challenges in remote clinical trial roles is maintaining effective communication and collaboration with research teams, participants, and stakeholders across various locations. This can be managed by utilizing secure collaboration tools, scheduling regular virtual check-ins, and following clear documentation practices. Remote professionals may also face difficulties in monitoring protocol compliance and data integrity without onsite presence, making strong organizational skills and familiarity with virtual monitoring tools essential. Being proactive and adaptable helps you address issues promptly and ensures study milestones are met. With the right support and resources, remote clinical trial professionals can seamlessly contribute to successful trial outcomes.

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What are the most commonly searched types of Clinical Trial jobs?

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What states have the most Remote Clinical Trial jobs?

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Remote Clinical Trial jobs near you
Infographic showing various Remote Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)

TMAC

Dallas, TX • Remote

Full-time

Posted 17 days ago

Job description

Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)

Serving as a value-added resource and extension of the Company, the Clinical Trial Liaison (CTL) will support the Company's Ophthalmology clinical trial pipeline. The CTL will serve as a clinical trial and clinical program subject matter expert and problem solver to help study sites optimize their study performance. The CTL will work full time to help sites address challenges in study delivery that could impact the Company's study or program goals.

This role involves compliant collaboration with KOLs, investigators, research staff members and CRO to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension of the clinical trial team to support ongoing studies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Site and Investigator Partnerships

  • Create investigator engagement plans to support site-specific recruitment, site identification and/or selection
  • Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention
  • Generate feasible, time-bound, prioritized action plans to address any barriers identified at clinical sites, document the plan and meet with the sites regularly to measure progress
  • Serve as a liaison to internal R&D and Clinical Operations functions to ensure the effective support of PIs
  • Collection of key medical insights from PIs to inform refinement of strategies

Building Company & Pipeline Advocacy

Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships

Expertise Management and Cross Functional Support

  • Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchanges with HCPs
  • Develop/increase knowledge of relevant medical literature and critical appraisal of scientific publications
  • Maintain knowledge base and scientific expertise on all assigned disease areas and products
  • Develop and update knowledge of applicable pharmaceutical guidelines and regulations. Code of Ethical Practices and company policies
  • Provide scientific input and participate in local medical and cross functional initiatives
  • Build scientific relationships with key thought leaders, healthcare professionals, investigators and their teams, government organizations, and patient and provider advocacy groups
  • Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives
  • Maintain working knowledge of regulatory and ethical requirements for all initiatives.

QUALIFICATIONS:

  • Knows how clinical sites operate, and has a history of helping study sites solve practical problems on clinical trials
  • Healthcare/science background inclusive of PharmD, PhD and MD, OD (or equivalent) required.
  • Clinical background in the area of Ophthalmology, with expertise in retinal diseases required
  • 5+ years of clinical research or clinical research support experience within academic, healthcare system or industry setting (e.g., clinical research coordinator, research manager, clinical research associate, study coordinator, research director) is required. Qualified individuals will have a strong familiarity and experience with clinical research and study site logistics.
  • Frequent travel is required. Availability to travel up to 50% of time
  • Availability to attend meetings on holidays and weekends
  • Clean and valid driver's license

Salary offers to be determined based on industry experience, education, and therapeutic expertise.

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