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Temporary Clinical Trials Test Subject Jobs (NOW HIRING)

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

The Clinical Trials Manager (CTM), Clinical Operations, coordinates the activities associated with ... and subject instructions • May participate in strategic governance discussions as required (e.g ...

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Temporary Clinical Trials Test Subject information

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$54

$89

How much do temporary clinical trials test subject jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for temporary clinical trials test subject in the United States is $54.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $81.49 per hour, depending on experience, location, and employer.

What is the difference between Temporary Clinical Trials Test Subject vs Clinical Research Coordinator?

AspectTemporary Clinical Trials Test SubjectClinical Research Coordinator
CredentialsNo formal certifications typically required; must meet trial-specific criteriaUsually requires a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentParticipates in clinical trials, often in medical facilities or research centersWorks in research sites, hospitals, or clinics managing trial operations
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding trial participation rolesManaging and coordinating clinical trials

The main difference is that Temporary Clinical Trials Test Subjects participate in trials without requiring extensive certifications, focusing on trial participation. Clinical Research Coordinators, however, manage and oversee the trial process, often needing relevant certifications and experience. Both roles are essential in clinical research but serve different functions within the industry.

More about Temporary Clinical Trials Test Subject jobs
What cities are hiring for Temporary Clinical Trials Test Subject jobs? Cities with the most Temporary Clinical Trials Test Subject job openings:
What are the most commonly searched types of Clinical Trials Test Subject jobs? The most popular types of Clinical Trials Test Subject jobs are:
What states have the most Temporary Clinical Trials Test Subject jobs? States with the most job openings for Temporary Clinical Trials Test Subject jobs include:
What job categories do people searching Temporary Clinical Trials Test Subject jobs look for? The top searched job categories for Temporary Clinical Trials Test Subject jobs are:
Temporary Clinical Trials Test Subject jobs near you
Infographic showing various Temporary Clinical Trials Test Subject job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

Clinical Trials Research Assistant

Vitreoretinal Surgery PLLC

Minneapolis, MN • On-site

$22 - $28/hr

Full-time

Medical, Dental, Life, PTO

Re-posted 14 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.