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Clinical Study Assistant Jobs in Provo, UT (NOW HIRING)

Reliant Rehabilitation

Physical Therapist

Payson, UT · On-site

$1.5K - $1.9K/wk

... clinical oversight and consultation to Physical Therapist Assistants (PTAs) Supervise PTAs and ... collaboration, self-study, and continuing education Maintain a valid state license and stay ...

Reliant Rehabilitation

Physical Therapist

Payson, UT · On-site

$40 - $55/hr

... • Provide clinical oversight and consultation to Physical Therapist Assistants (PTAs) • ... self-study, and continuing education • Maintain a valid state license and stay informed on ...

Reliant Rehabilitation

Physical Therapist

Payson, UT · On-site

$40 - $55/hr

... • Provide clinical oversight and consultation to Physical Therapist Assistants (PTAs) • ... self-study, and continuing education • Maintain a valid state license and stay informed on ...

Reliant Rehabilitation

Physical Therapist

Payson, UT · On-site

$1.5K - $1.9K/wk

... • Provide clinical oversight and consultation to Physical Therapist Assistants (PTAs) • ... self-study, and continuing education • Maintain a valid state license and stay informed on ...

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All JobsClinical Study JobsClinical Study Assistant JobsClinical Study Assistant Jobs in Provo, UT

Clinical Study Assistant information

See Provo, UT salary details

$10

$19

$27

How much do clinical study assistant jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical study assistant in Provo, UT is $19.14, according to ZipRecruiter salary data. Most workers in this role earn between $15.67 and $22.07 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

What is the difference between Clinical Study Assistant vs Clinical Research Coordinator?

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What are the most commonly searched types of Clinical Study jobs in Provo, UT?

The most popular types of Clinical Study jobs in Provo, UT are:

Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Provo, UT as of August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 16% Part Time, and 7% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $39,806 per year, or $19.1 per hour.

Phlebotomist/Medical Assistant

IVI RMA North America

Sandy, UT • On-site

$17 - $21.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 11 days ago

Job description

IVI RMA North America hosts a network of state-of-the-art fertility practices in the United States

Join a collaborative fertility clinic team where patient care, compassion, and attention to detail matter. Our Sandy, UT office is seeking a Phlebotomist/Medical Assistant who enjoys hands-on patient interaction and wants to grow in women’s health and reproductive medicine. This is a great opportunity for someone early in their healthcare career who is looking to build clinical experience in a supportive and highly specialized environment.

Hours Monday through Friday 7 am – 3:30 pm or 8 am - 4:30 pm, depending on the needs of the office, with rotating weekends and holidays.

Apply today to start your career working in a state-of-the-art facility supporting women’s health experience within the fertility industry.

The Medical Assistant will promote and restore patients’ health by assisting in the nursing process and supporting physicians and other multidisciplinary team members with hands-on patient care. You will help to create a positive experience for our patients and ensure that patients receive high-quality service by assisting clinical team with patient care.  

Essential Functions and Accountabilities: 

  • Assist Physicians with clinical procedures
  • Follow proper protocols for all procedures
  • Practice phlebotomy 
  • Accurately document ultrasound measurements, provider comments and use appropriate stim templates while chaperoning ultrasounds.
  • Clean exam rooms and equipment per protocol.
  • Set up and stock examination and procedure rooms.
  • Maintain clinical supplies inventory.
  • Specimen collection, processing for in-house and outside laboratories.
  • Manage Lanfax for outside labs, reports, results. Enter results and email to provider team for review.
  • Provide patients with information regarding upcoming procedures and reassurance/comfort before, during and after procedures.

 

Academic Training:

  • Completion of Certified Medical Assistant Program – preferred
    1. Studies level: Certification
    2. Studies area: Nursing/healthcare assistant
  • Phlebotomy Program – preferred
    • Studies level: Certification
    • Studies area: Phlebotomy Program

 

Position Requirements/Experience: 

  • 6+ months experience as a Medical Assistant in a physician practice
  • Prior experience in women’s healthcare – preferred
  • Must be able to work weekends, holidays, and occasional evenings

Technical Skills: 

  • Knowledge of Microsoft Office, especially Outlook and Excel – required
  • EMR experience - preferred

IVI-RMA offers a comprehensive benefits package to all employees who work a minimum of 30 hours per week.

  • Medical, Dental, Vision Insurance Options
  • Retirement 401K Plan
  • Paid Time Off & Paid Holidays
  • Company Paid: Life Insurance & Long-Term Disability & AD&D
  • Flexible Spending Accounts
  • Employee Assistance Program
  • Tuition Reimbursement


About IVIRMA Global:  

IVIRMA is the largest group in the world devoted exclusively to human Assisted Reproduction Technology. Along with the great privilege of providing fertility care to our patients, IVIRMA embraces the great responsibility of advancing the field of human reproduction. IVIRMA Innovation, as one of the pillars of IVIRMA Global, is a renowned leader in fertility research and science. Check out our websites at: https://rmanetwork.com/ & https://www.ivirma.com/

EEO
 “IVIRMA is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: IVIRMA is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at IVIRMA are based on business needs, job requirements and individual qualifications, without regard to race, color, religion and/or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. IVIRMA will not tolerate discrimination or harassment based on any of these characteristics. IVIRMA encourages applicants of all ages.”



Monday - Friday 7am-3:30pm or 8 am-4:30pm, varying depending on needs of the office. Weekend and holiday rotation.