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Paid Clinical Trials Jobs (NOW HIRING)

Gilead

Sr Clinical Trials Manager

Foster City, CA · On-site

$157K - $203K/yr

The Senior Clinical Trials Manager leads studies within a program, provides direction to Clinical ... paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision ...

Gilead

Sr Clinical Trials Manager

Foster City, CA · On-site +1

$157K - $203K/yr

Clinical Operations leads the global execution of Phase I-IV clinical trials across therapeutic ... paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision ...

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How much do paid clinical trials jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for paid clinical trials 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 are paid clinical trials?

Paid clinical trials are research studies where participants receive financial compensation for their time and involvement. These trials are conducted to test the safety and effectiveness of new drugs, treatments, or medical devices before they are approved for public use. Participants may be healthy volunteers or individuals with specific medical conditions, and compensation can vary depending on the length and type of study. Payment is intended to cover time, travel, and other related expenses, not to influence participation or risk.

What are the typical responsibilities of a clinical trial participant?

As a participant in paid clinical trials, you can expect to follow a specific study protocol, which may include taking medications, attending scheduled clinic visits, and undergoing regular health assessments. You will be asked to provide honest feedback about your experience and report any side effects you notice. The process typically involves initial screening, informed consent, and continuous monitoring by a clinical team. Open communication with research staff is essential to ensure your safety and the integrity of the trial. Participation offers unique insights into medical research and may contribute to advancements in healthcare.

What skills and qualifications are needed to participate in paid clinical trials?

To thrive as a Clinical Trial Participant, you need to meet specific eligibility criteria, such as health status and age, and demonstrate reliability in following study protocols. Familiarity with informed consent procedures and the ability to accurately report health changes or side effects are important. Commitment, attention to detail, and clear communication with research staff are valuable soft skills. These skills and qualities ensure participant safety, data integrity, and the overall success of the clinical research study.
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Paid Clinical Trials jobs near you
Infographic showing various Paid Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, and 2% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trials Research Assistant

Vitreoretinal Surgery PLLC

Minneapolis, MN

$22 - $28/hr

Full-time

Medical, Dental, Life, PTO

Re-posted 27 days ago

Job description

Apply Here: https://secure.onehcm.com/ta/VRSPLLC.jobs?ShowJob=587374149&TrackId=ZipRecruiter

We are seeking multiple outgoing, patient focused individuals to work as Clinical Trials Research Assistant at our Retina Consultants of Minnesota Edina, MN clinic.
Responsibilities for an Clinical Trials Research Assistant include:
  • Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
  • Prepare visit-specific documentation and charts for Clinical Research Coordinator
  • Observe Coordinator in patient care and management
  • Assist Coordinator in monitoring subject flow and assist in subject care and management
  • Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy)
  • Transcribe subject study information from source documents to the Electronic Case Report Forms
  • Administer all mandatory questionnaires to study subjects
  • Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol
  • Promptly request all necessary medical records for Serious Adverse Event Reporting
  • Process and ship laboratory biological samples for analysis
  • Perform intraocular pressure checks after injections
  • Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites)
  • Inform subjects and obtain written re-consents in regard to ICF’s
Required Skills, Abilities and Attributes:
  • Applicants MUST be personally motivated to provide excellent patient care!
  • 1+ years of clinical trials research assistant experience in a retina or general ophthalmology environment preferred
  • Knowledge of medical terminology
  • Be an excellent team player who works cooperatively and respectfully with all doctors, supervisors and co-workers
  • Displays a desire to perpetually “Learn and Grow”
  • Efficient and highly accurate user of applicable information technology and health care management systems
  • High School Degree or GED
We offer excellent compensation and benefits, to include:
  • Paid Holidays - 7 days per year
  • Personal Time Off (PTO) - 16 days per year
  • Health Insurance
  • Health Reimbursement Account
  • Health Savings Account
  • Dental Insurance (free single coverage)
  • Flexible Spending Accounts
  • Basic and Supplemental Term Life Insurance (free single coverage)
  • Long Term Disability (free single coverage)
  • Long Term Care (free single coverage)
  • Short-Term Disability
  • Vision
  • Annual $250 uniform (scrubs and shoes) reimbursement
About Retina Consultants of Minnesota (RCM):
RCM has 9 Minnesota locations - St. Louis Park, Edina, Edina Specialty, Woodbury, Blaine, Duluth, Maplewood, Anoka and Mankato.
Everything we do…. every decision we make…takes our Guiding Principles into consideration. Our guiding principles are:
  • We exist to serve our patients. We will provide the best available medical skills, technology, and service. We will be their advocates. We will care for our patients as if they were members of our family. We will treat our patients with respect, dignity, and kindness.
  • We are proud of our dedicated staff. We will strive to provide a rewarding career with opportunity for personal and professional growth. We will promote teamwork. We will provide a respectful and safe working environment.
  • We are humbled that other doctors entrust their patients to our care. We will be available when we are needed. We will promptly communicate the results of patient evaluation and treatment. We will respect the referring doctors’ relationships with their patients.
  • We recognize that we have a responsibility to our community. We will strive to be desire to perpetually “Learn and Grow”
  • Efficient and highly accurate user of applicable information technology and health care management systems
  • A good corporate citizen. We will function ethically. We will be prudent in our stewardship of healthcare resources.
  • Medical advances are critical to our patients. We will remain at the forefront in the search for new knowledge and treatments of retinal disease. We will participate in clinical research. We will share our knowledge with our patients and referring doctors, and with our retinal colleagues around the world.