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Full Time Clinical Study Startup Jobs (NOW HIRING)

Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary M ... Responsibilities Clinical Study Coordinator, II Coordinate fundamental technical and administrative ...

Clinical Study Coordinators

Campus, IL · On-site

$48K - $56K/yr

Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary M ... Clinical Study Coordinator, II: Requires a bachelor's (or equivalency) + 4 years or a master's (or ...

Clinical Study Coordinators

Campus, IL · On-site

$48K - $56K/yr

Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary M ... Clinical Study Coordinator, II: Requires a bachelor's (or equivalency) + 4 years or a master's (or ...

This role will establish scalable approaches for feasibility, site identification, study startup ... These benefits are offered exclusively to permanent full-time employees. Contractors are not ...

Clinical Study Manager

Irvine, CA · On-site +1

$114.95K - $165K/yr

Responsibilities The Clinical Study Manager (CSM) is responsible for the operational management and ... Employment Type: FULL_TIME

Orange County Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing ...

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Full Time Clinical Study Startup information

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How much do full time clinical study startup jobs pay per hour?

As of May 28, 2026, the average hourly pay for full time clinical study startup 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 the key skills and qualifications needed to thrive as a Full Time Clinical Study Startup professional, and why are they important?

To thrive as a Full Time Clinical Study Startup professional, you need a strong background in clinical research, regulatory requirements, and project management, often supported by a life sciences degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), regulatory documentation platforms, and Good Clinical Practice (GCP) certification is typically required. Exceptional organizational skills, attention to detail, and effective communication are vital soft skills for coordinating stakeholders and ensuring study timelines are met. These competencies are essential for ensuring the compliant, efficient, and timely initiation of clinical studies.

What are some common challenges faced during the clinical study startup phase, and how can they be addressed?

One common challenge in clinical study startup roles is coordinating timelines between multiple stakeholders, such as regulatory bodies, ethics committees, and site staff. Delays often occur due to incomplete documentation or differing site requirements. Effective communication, proactive planning, and familiarity with regulatory processes are key to overcoming these obstacles. Working closely with cross-functional teams and maintaining detailed trackers can help ensure a smoother and faster study initiation.

What is a Full Time Clinical Study Startup role?

A Full Time Clinical Study Startup role involves overseeing and coordinating the initial phases of clinical trials, such as site selection, regulatory document collection, ethics submissions, and study initiation activities. Professionals in this position ensure that all necessary approvals and documentation are in place to begin the clinical study on schedule. They work closely with clinical research teams, investigators, and regulatory bodies to manage timelines and compliance with applicable guidelines. This role is crucial for ensuring that clinical trials start efficiently and adhere to all regulatory requirements.
More about Full Time Clinical Study Startup jobs
What cities are hiring for Full Time Clinical Study Startup jobs? Cities with the most Full Time Clinical Study Startup job openings:
What are the most commonly searched types of Clinical Study Startup jobs? The most popular types of Clinical Study Startup jobs are:
What states have the most Full Time Clinical Study Startup jobs? States with the most job openings for Full Time Clinical Study Startup jobs include:
Clinical Study Coordinators

Clinical Study Coordinators

University of Utah

Salt Lake City, UT • On-site

$48K/yr

Full-time

Retirement

Posted 15 days ago


University Of Utah rating

7.2

Company rating: 7.2 out of 10

Based on 157 frontline employees who took The Breakroom Quiz

327th of 528 rated colleges and universities


Job description

Announcement
Details
Open Date
04/21/2026
Requisition Number
PRN44844B
Job Title
Clinical Study Coordinators
Working Title
Trauma Study Coordinator
Career Progression Track
P00
Track Level
P2 - Developing
FLSA Code
Administrative
Patient Sensitive Job Code?
Yes
Standard Hours per Week
40
Full Time or Part Time?
Full Time
Shift
Day
Work Schedule Summary
M-F
VP Area
U of U Health - Academics
Department
00269 - Orthopedic Surgery Operations
Location
Campus
City
Salt Lake City, UT
Type of Recruitment
External Posting
Pay Rate Range
$48K
Close Date
06/21/2026
Priority Review Date (Note - Posting may close at any time)
Job Summary
Helps with the logistical and administrative aspect of clinical trials and studies, ensuring adherence to protocols and regulatory requirements. Help facilitate participant recruitment, consent processes, and documentation management. Coordinate study visits, monitor adverse events, and maintain accurate records for successful study outcomes.
Responsibilities
Clinical Study Coordinator, II
Coordinate fundamental technical and administrative details in clinical trials or research studies with some supervision. Assist Principal Investigators in achieving study objectives by implementing and completing study protocols and procedures. Review protocols for clarity and subject safety, addressing concerns with the PI and sponsor. Participate in recruitment and consent processes. Maintain detailed and accurate study documentation. Coordinate study visits and ensure the availability of necessary resources. Report and track adverse events with guidance. Complete and audit CRFs for accuracy. Assist in preparing and submitting IRB documents. Ensure proper collection, processing, and shipment of specimens.
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.
This is a Developing-Level position in the General Professional track.
Job Code: PZ1732
Grade: P11
Minimum Qualifications
EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor's degree = 4 years of directly related work experience).
Department may hire employee at one of the following job levels:
Clinical Study Coordinator, II: Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.
Preferences
Requires a bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree. Assumes work equivalency (1 year of higher education ca be substituted for 1 year of directly related work experience)
Type
Benefited Staff
Special Instructions Summary
Additional Information
The University is a participating employer with Utah Retirement Systems ("URS"). Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work). Contact Human Resources at (801) 581-7447 for information. Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS' post-retirement rules and restrictions. Please contact Utah Retirement Systems at (801) 366-7770 or (800) 695-4877 or University Human Resource Management at (801) 581-7447 if you have questions regarding the post-retirement rules.
This position may require the successful completion of a criminal background check and/or drug screen.
The University of Utah values candidates who have experience working in settings with students and possess a strong commitment to improving access to higher education.
Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities.
Consistent with state and federal law, the University of Utah does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status. The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106. The requirement not to discriminate in education programs or activities extends to admission and employment. Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both.
To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Title IX (OEO). More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at the: University of Utah Non-Discrimination page.
Online reports may be submitted at https://oeo.utah.edu
https://publicsafety.utah.edu/safetyreport/ This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses. They also provide information about safety and security-related services offered by the University of Utah. A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South.
As per University of Utah policy 5-108: Transfer of Benefits Eligible Staff Members, a new hire to the University of Utah who is still serving a 12 month probationary period will not be hired into another University of Utah job (a transfer) until the successful completion of the probationary period.

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About University of Utah

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The University of Utah is the state’s flagship institution of higher education, with 18 schools and colleges, more than 100 undergraduate majors and graduate programs, and an enrollment of more than 38,000 students. It is a member of the Association of American Universities—an invitation-only, prestigious group of 71 leading research institutions. The U is advancing a new national model for higher education that delivers societal impact through education, research, health care, and community service, while making social, economic, and cultural contributions that improve lives across Utah and around the world.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Salt Lake City, UT, US

Year founded

1850