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Freelance Clinical Research Remote Jobs (NOW HIRING)

IQVIA

Freelance Independent Rater

London, OH · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Boston, MA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Los Angeles, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

New Providence, NJ · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Houston, TX · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

San Francisco, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

New York, NY · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

New York, NY · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Washington, DC · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Houston, TX · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Washington, DC · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

IQVIA

Freelance Independent Rater

Los Angeles, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

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Freelance Clinical Research Remote information

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How much do freelance clinical research remote jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for freelance clinical research remote in the United States is $30.16, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $31.97 per hour, depending on experience, location, and employer.

What is a freelance clinical research remote?

A Freelance Clinical Research Remote job involves working independently on clinical research projects from a location outside of a traditional office, usually from home. Professionals in this role support the planning, execution, and monitoring of clinical trials for drugs, devices, or medical interventions. Typical tasks may include data collection, regulatory documentation, study coordination, and analysis. Freelancers can work with multiple clients or organizations, offering flexibility and the opportunity to manage their workload and schedule. This arrangement is ideal for experienced clinical research professionals seeking autonomy and remote work opportunities.

What are the key skills and qualifications needed to thrive as a freelance clinical research professional working remotely?

To thrive as a Freelance Clinical Research professional in a remote setting, you need expertise in clinical trial processes, data analysis, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are typically required. Strong communication, self-motivation, and organizational skills help you efficiently coordinate with diverse teams and manage multiple projects independently. These skills and qualifications are vital to ensure accurate research outcomes, maintain compliance, and deliver effective results while working remotely.

How do freelance clinical research professionals typically collaborate with sponsors and study teams while working remotely?

Freelance clinical research professionals often use a variety of digital tools to stay connected with sponsors, CROs, and study teams. Regular virtual meetings, shared project management platforms, and secure document exchange systems are common for coordinating tasks, addressing queries, and ensuring consistent project updates. Clear communication and proactive scheduling are crucial, as freelancers must be self-motivated to meet deadlines and promptly report progress. Building reliable relationships remotely requires responsiveness and transparency, which helps maintain trust and project momentum.

What is the difference between Freelance Clinical Research Remote vs Clinical Research Coordinator?

AspectFreelance Clinical Research RemoteClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences or related field; often holds certifications like CCRP or RAC
Work EnvironmentRemote, flexible; project-based assignments for multiple clientsOn-site or hybrid at research sites or hospitals
Employer & Industry UsageFreelance basis, used by contract research organizations, pharma companies, or independent consultantsEmployed by research sites, hospitals, or CROs to coordinate clinical trials

Freelance Clinical Research Remote professionals work independently, often remotely, managing multiple projects for various clients. Clinical Research Coordinators typically work on-site at research facilities, coordinating daily trial activities. Both roles require similar credentials but differ mainly in work setting and employment structure.

More about Freelance Clinical Research Remote jobs

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States with the most job openings for Freelance Clinical Research Remote jobs include:

What job categories do people searching Freelance Clinical Research Remote jobs look for?

The top searched job categories for Freelance Clinical Research Remote jobs are:

Freelance Clinical Research Remote jobs near you
Infographic showing various Freelance Clinical Research Remote 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 $62,726 per year, or $30.2 per hour.

Clinical Research Manager

Johns Hopkins University

Baltimore, MD • On-site, Remote

$55K - $97K/yr

Full-time

Re-posted 8 days ago

Johns Hopkins University rating

8.0

Company rating: 8.0 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

188th of 618 rated colleges and universities

Job description

The Department of Neurology is seeking a Clinical Research Manager who will deliver and organize work plans with 20+ clinical sites across the country in support of clinical trial research goals of the BIOS Clinical Trials Coordinating Center's (CTCC).
Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. The Clinical Research Manager works under the general supervision of a Pl(s) to manage the administrative and scientific implementation of a complex clinical protocol or multiple studies and/or multiple sites. As part of a study team, collaborate with faculty, develop protocols, develop SOPs, and supervise study-related activities for one or more studies. Has accountability for grant submission and administration and regulatory compliance. Supervise or oversee other exempt level research staff; may oversee staff at local or multi-center sites.
Specific Duties & Responsibilities
  • Partner with investigator(s) and exercise independent judgement in managing the conduct of the research on behalf of the Pl.
  • Participate in scientific discussions with collaborators, Pl's, and funding organizations.
  • Collaborate with Pl to ensure operational feasibility of proposed protocol/study design.
  • Develop, or oversee the development of standard operating procedures and data collection forms from protocol(s).
  • Develop or oversee the development of consent form(s) for clinical trials based on protocol(s).
  • Oversee preparation and submissions to IRB and act as primary liaison for regulatory compliance issues on behalf of the Pl.
  • Train and provide oversight of research data management and regulatory issues.
  • Work with commercial and/or government agency sponsors to determine what group can commit to considering patient population, available resources, and cost of providing services.
  • Collaborate with the finance team to develop study budget(s) and ensure that all study costs are included in the budget.
  • Ensure clinical research protocol has a completed Prospective Reimbursement Analysis {PRA) and processes/systems are in place to ensure the PRA is followed when required.
  • Ensure adequate system for tracking and reporting clinical research milestones for financial invoicing.
  • Monitor activities, systems, and processes to increase referrals and increase accruals to clinical trials.
  • Ensure the development, testing, and evaluation of manuals, questionnaires, and coding structures, for the efficient collection of data.
  • Oversee data collection at a single site or at multiple sites of a multi-centered clinical trial.
  • Lead study meetings to examine data, determine next steps, implement changes to protocol operations based on results and goals, and initiate sub-studies.
  • Contribute to presentations and manuscripts.
  • Hire, supervise and manage performance of other exempt-level research staff.
  • Other duties as assigned.

Minimum Qualifications
  • Bachelor's Degree in a related field.
  • Five years of related experience in clinical research in an academic,
  • Strong organizational, analytical, and leadership skills with experience in multi-site coordination.
  • Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Preferred Qualifications
  • Master's Degree in a related field.
  • Certification as a Clinical Research Professional.
  • Formal project management training or certification.
  • Advanced knowledge of GCP/ICH and local regulations.
  • Proficiency in Microsoft Office Suite and SharePoint; ability to learn new software (e.g., eIRB, EDC systems).

Technical Skills & Expected Level of Proficiency
  • Budget Management - Advanced
  • Clinical Study Design - Advanced
  • Good Clinical Practices - Advanced
  • Interpersonal Skills - Advanced
  • Oral and Written Communications - Advanced
  • Project Management - Advanced
  • Record Keeping - Advanced
  • Regulatory Compliance - Advanced
  • Strategic Planning - Advanced

The core technical skills listed are most essential; additional technical skills may be required based on specific division or department needs.
Classified Title: Clinical Research Manager
Job Posting Title (Working Title): Clinical Research Manager
Role/Level/Range: ACRP/04/MD
Starting Salary Range: $55,800 - $97,600 Annually ($76,700 targeted; Commensurate w/exp.)
Employee group: Full Time
Schedule: M-F 8:30 am - 5:00 pm
FLSA Status: Exempt
Location: Remote
Department name: SOM Neuro BIOS
Personnel area: School of Medicine

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