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Remote Clinical Trial Operations Jobs (NOW HIRING)

ICON

Clinical Trial Manager

Blue Bell, PA · On-site +1

Clinical Operations Lead - Hematology/Von Willebrand Disease ICON is a global healthcare ... Clinical Operations Lead (CTM) The Clinical Operations Lead supports the Clinical Trial Manager ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

The successful candidate will manage members of the clinical operations team, including those at ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

UAB

CLINICAL RESEARCH REGULATORY COORDINATOR III

Tampa, FL · Remote

$55K - $89K/yr

... clinical trial operations. * To design and implement quality initiatives ensuring effective and ... Provides ongoing remote clinical monitoring assistance to study sites. * Provides recommendations ...

ICON

Clinical Trial Manager II

Blue Bell, PA · On-site +1

Clinical Trial Manager - early oncology ICON is a global healthcare intelligence and clinical ... Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ...

Oran Inc

Clinical SME I

Herndon, VA · Remote

Position Title Clinical SME I Overview We are seeking a Clinical Subject Matter Expert (SME) with extensive experience in clinical trial operations, FDA regulatory processes, and protocol development.

Oran Inc

Clinical SME I

Herndon, VA · Remote

Position Title Clinical SME I Overview We are seeking a Clinical Subject Matter Expert (SME) with extensive experience in clinical trial operations, FDA regulatory processes, and protocol development.

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... This position is for remote work and may require domestic or international travel up to 25% (as ...

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Remote Clinical Trial Operations information

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How much do remote clinical trial operations jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for remote clinical trial operations in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trial Operations vs Remote Clinical Trial Coordinators?

AspectRemote Clinical Trial OperationsRemote Clinical Trial Coordinators
ResponsibilitiesOversees trial processes, manages site logistics, ensures complianceSupports trial activities, manages participant schedules, assists with data collection
Required CredentialsTypically requires a degree in life sciences, clinical research certificationOften requires a degree or certification in clinical research or related field
Work EnvironmentRemote, with collaboration across sites and teamsPrimarily remote, working closely with trial sites and participants
Industry UsageCommon in pharmaceutical and biotech companiesCommon in research organizations and CROs

Remote Clinical Trial Operations professionals focus on managing and overseeing the entire trial process, ensuring compliance and efficiency. In contrast, Remote Clinical Trial Coordinators handle day-to-day participant management and data collection. Both roles require clinical research knowledge and often work remotely, but their scope and responsibilities differ significantly.

More about Remote Clinical Trial Operations jobs
What cities are hiring for Remote Clinical Trial Operations jobs? Cities with the most Remote Clinical Trial Operations job openings:
What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Remote Clinical Trial Operations jobs? States with the most job openings for Remote Clinical Trial Operations jobs include:
What job categories do people searching Remote Clinical Trial Operations jobs look for? The top searched job categories for Remote Clinical Trial Operations jobs are:
Remote Clinical Trial Operations jobs near you
Infographic showing various Remote Clinical Trial Operations job openings in the United States as of June 2026, with employment types broken down into 15% Full Time, and 85% Part Time. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Clinical Trial Manager

Clinical Trial Manager

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 22 days ago

Job description

Clinical Operations Lead - Hematology/Von Willebrand Disease
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-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Clinical Operations Lead (CTM)
The Clinical Operations Lead supports the Clinical Trial Manager/operational team in execution of the trial (s). The position includes direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks. The Lead maintains effective communication with project team through oral and written correspondence, status reports to ensure alignment with study timelines.
  • Assist in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents.
  • Create Master ICF template and review/approve site changes (in consultation with legal, safety when warranted). Update template for new risks and new amendments information.
  • Participate in the feasibility and evaluation of investigative sites; working closing with the Clinical Trial Logistics group.
  • Coordinate and monitor activities at investigational sites; review monitoring trip reports and support the US monitoring organization.
  • Assist in the development and management of study timelines and priorities, including recruitment tools/strategy and patient retentions plan.
  • Plan and organized meetings with team support (eg. investigator/coordinator meetings, DMC, SMC, safety call, etc.).
  • Assist in the development of the IP and co-medication strategy (Quantities, labels, depots, tracking, etc.) working closely with other departments.
  • Participate in data review and discrepancy resolution.
  • Participate in coordinating efforts with internal Pharmacovigilance, and safety group.
  • Monitor study-specific timelines and key deliverables; focus on management of all external vendors (e.g Monitoring, Sample management, IVRS, Laboratory, etc).
  • Participate as a member of the multi-disciplinary trial(s) team.
  • Develop relationships with investigational sites and institutions to enhance conduct of the trial.
  • Acts as preliminary liaison for study sites to convey trial information, answer questions and in accordance with the escalation pathway.
  • Assume responsibility to participate as a member of a working group and perform special projects, as assigned, to improve the efficiency, effective and quality of the functioning of the Development Operations Department.

What you need to have:
  • BS/BA degree or a relevant degree with strong emphasis on science.
  • Minimum of 5 years of clinical trial management experience in the biopharmaceutical industry or other relevant clinical research experience.
  • Candidates must have non-malignant hematology clinical trial management experience/Von Willebrand disease
  • Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health authority experience.
  • Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
  • Prior experience in assisting the conduct and management of multinational clinical trials is preferred.
  • To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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