1

Contract Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Wichita, KS · On-site

$21.75 - $28.75/hr

Clinical Research Coordinator DEPARTMENT: Clinical Research LOCATION: Wichita, KS PERKS * Full ... Understand the operational budget and sub-contracts; track documentation and authorization of ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in ...

Work Environment This is a part-time contract role of approximately 20 hours per week for about 7 months, based on-site at a clinical research facility in Mobile, AL. The position follows normal ...

... contract issues; initiates regulatory activities; oversees preparation of necessary project ... Participates in selection process of clinical research unit staff; provides training to research ...

Clinical Research Nurse

Mobile, AL · On-site

$35 - $42/hr

Work Environment This is a part-time contract role of approximately 20 hours per week for about 7 months, based on-site at a clinical research facility in Mobile, AL. The position follows normal ...

Showing results 41-60

Contract Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do contract clinical research jobs pay per year?

As of Aug 16, 2026, the average yearly pay for contract clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a contract clinical research?

A Contract Clinical Research job involves working on a temporary or project-based basis to support clinical trials and research studies. Professionals in this role ensure compliance with regulatory standards, oversee study protocols, and manage data collection and reporting. They often work for pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. These roles require expertise in clinical trial processes, good clinical practices (GCP), and regulatory guidelines. Contract positions vary in duration and may offer flexibility in location and work arrangements.

What are the key skills and qualifications needed to thrive in the contract clinical research position, and why are they important?

To thrive in Contract Clinical Research, you need a strong background in clinical trial processes, regulatory compliance (such as GCP/ICH guidelines), and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like CCRA or CCRC are often required. Excellent organizational, communication, and problem-solving skills are vital for managing multiple projects and collaborating with cross-functional teams. These abilities ensure the smooth and ethical conduct of clinical trials while meeting tight timelines and quality standards.

What are the typical day-to-day responsibilities for someone in a contract clinical research role?

In a Contract Clinical Research position, you will typically oversee the execution of clinical trials, which includes tasks such as monitoring study sites, ensuring regulatory and protocol compliance, and managing study documentation. You'll collaborate closely with principal investigators, sponsors, and clinical site staff to ensure timelines are met and data is collected accurately. Responsibilities may also include preparing reports, assisting with site selection or initiation, and resolving any study-related issues that arise. This dynamic role often requires balancing administrative, technical, and interpersonal tasks to successfully support clinical research projects.

More about Contract Clinical Research jobs

What cities are hiring for Contract Clinical Research jobs?

Cities with the most Contract Clinical Research job openings:

What are the most commonly searched types of Clinical Research jobs?

The most popular types of Clinical Research jobs are:

What states have the most Contract Clinical Research jobs?

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

Infographic showing various Contract Clinical Research 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 $107,336 per year, or $51.6 per hour.

Full-time

Medical, Retirement, PTO

Posted 5 days ago


UT Southwestern rating

7.9

Company rating: 7.9 out of 10

Based on 152 frontline employees who took The Breakroom Quiz

108th of 887 rated healthcare providers


Job description

WHY UT SOUTHWESTERN?
With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!
JOB SUMMARY
Works under limited supervision to be responsible for directing all administrative and research functions of clinical research unit(s).

BENEFITS
UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

  • PPO medical plan, available day one at no cost for full-time employee-only coverage
  • 100% coverage for preventive healthcare-no copay
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer
  • Learn more about these and other UTSW employee benefits!

EXPERIENCE AND EDUCATION
Required
  • Education
    Bachelor's Degree in science, social science, business, health-related (including nursing) field or
    Master's Degree in science, social science, business, or health-related (including nursing) field or
    PhD or equivalent in science, social science, business, or health-related (including nursing) field
  • Experience
    6 years of related experience to include management experience with Bachelor's Degree or
    4 years of related experience to include management experience with Master's Degree or
    3 years of related experience to include management experience with PhD.
Preferred
  • Experience
    Prior experience in the UTSW clinical research mentoring program is highly desirable, and participation in the UTSW clinical research mentoring program may count as additional experience.
  • Licenses and Certifications
    (BLS) BASIC LIFE SUPPORT may be required based on research study protocols or affiliate location requirements.
    (CPRAED) CPR AED may be required based on research study protocols or affiliate location requirements.

JOB DUTIES
  • Reviews proposed new research studies and determines projects to implement; negotiates budget and contract issues; initiates regulatory activities; oversees preparation of necessary project summaries, consent forms, etc. for IRB; oversees compliance with all regulatory requirements.
  • Oversees on-going research studies and quality assurance measures, developing criteria where necessary; negotiates favorable agreements with laboratories and collaborators on campus; monitors profitability of research studies; renegotiates contracts, supplements, etc. as needed.
  • Directs financial oversight and management of clinical research unit; ensures invoicing is accurate and sponsor payments are received; ensures appropriateness of expenditures from various funding sources available to clinical research unit.
  • Participates in selection process of clinical research unit staff; provides training to research, financial, laboratory, and administrative staff; evaluates staff performance and implements measures necessary to maintain quality performance and results; participates in training, development, and/or disciplinary measures; assesses policies and procedures to ensure optimal operation of clinical research unit.
  • Identifies potential sponsors for clinical research unit; develops and oversees marketing strategies.
  • Initiates and maintains collaborative relationships between clinical research unit and basic science facilities.
  • Designs, executes, and maintains effective system of internal controls which provides reasonable assurance that operations are effective and efficient, assets are safeguarded, and financial information is reliable.
  • Ensures compliance with applicable laws, regulations, policies, and procedures.
  • Duties performed may include one or more of the following core functions: a) Directly interacting with or caring for patients; b) Directly interacting with or caring for human-subjects research participants; c) Regularly maintaining, modifying, releasing or similarly affecting patient records (including patient financial records); or d) Regularly maintaining, modifying, releasing or similarly affecting human-subjects research records.
  • Performs other duties as assigned.

SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
EEO
UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

What UT Southwestern employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom