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Associate Clinical Research Coordinator Jobs (NOW HIRING)

Stryde Research

Clinical Research Coordinator

Plano, TX · On-site

$50K - $80K/yr

The Clinical Research Coordinator will oversee and manage clinical research studies, ensuring compliance with protocols and regulations. Responsibilities include obtaining informed consent from ...

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How much do associate clinical research coordinator jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for associate clinical research coordinator in the United States is $28.69, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.01 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to thrive as an associate clinical research coordinator?

To thrive as an Associate Clinical Research Coordinator, you need a background in life sciences or a related field, knowledge of clinical trial processes, and an understanding of regulatory requirements. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and possibly certifications like SOCRA or ACRP are typical technical assets. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating studies and interacting with diverse teams. These skills ensure studies are conducted accurately, ethically, and efficiently, supporting both compliance and successful trial outcomes.

What are the primary challenges an associate clinical research coordinator might face during a clinical trial?

One common challenge for Associate Clinical Research Coordinators is managing multiple tasks and tight timelines, as they often handle patient recruitment, data entry, and regulatory documentation simultaneously. Additionally, ensuring strict adherence to study protocols and regulatory guidelines can be complex, especially when unexpected issues arise with participants or data collection. Effective communication with the research team, principal investigators, and study participants is essential to navigate these challenges successfully and maintain the integrity of the trial.

What is an associate clinical research coordinator?

Associate Clinical Research Coordinators are entry-level professionals who assist in the planning, implementation, and management of clinical trials and research studies. They support lead coordinators and principal investigators by handling tasks such as recruiting participants, collecting and entering data, ensuring regulatory compliance, and maintaining study documentation. Their role is crucial in ensuring that clinical trials run smoothly and adhere to ethical and legal standards. Associate Clinical Research Coordinators often work in hospitals, universities, or research organizations, and their work helps advance medical knowledge and patient care.
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Associate Clinical Research Coordinator jobs near you
Infographic showing various Associate Clinical Research Coordinator job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $59,666 per year, or $28.7 per hour.

Clinical Research Coordinator

PRIME CLINICAL RESEARCH INC

Mansfield, TX • On-site

$21.75 - $29/hr

Full-time

Re-posted 11 days ago

Job description

About the Role:
Join PRIME CLINICAL RESEARCH INC as a Clinical Research Coordinator in Mansfield, TX, where you'll play a vital role in advancing medical research. This exciting position offers the opportunity to work on innovative clinical trials while collaborating with a passionate team dedicated to improving patient outcomes.
Responsibilities:
  • Coordinate and manage clinical trial activities to ensure compliance with study protocols.
  • Recruit, screen, and enroll study participants while maintaining accurate records.
  • Conduct informed consent discussions and provide education to participants.
  • Monitor patient progress and collect data throughout the trial phases.
  • Collaborate with investigators and regulatory bodies to ensure adherence to guidelines.
  • Prepare and submit necessary documentation to ethics committees and regulatory agencies.
  • Facilitate communication between study participants, sponsors, and team members.
  • Assist in the training and mentoring of new staff members as needed.
Requirements:
  • Bachelor’s degree in life sciences or a related field preferred.
  • Previous experience in clinical research or as a clinical research coordinator.
  • Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
  • Excellent organizational skills and attention to detail.
  • Effective communication and interpersonal skills to work with diverse teams.
  • Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
  • Certification in Clinical Research (e.g., ACRP or SOCRA) is a plus.
  • Proficient in Microsoft Office Suite and clinical trial management software.
About Us:
PRIME CLINICAL RESEARCH INC has been at the forefront of clinical research in DFW Area, dedicated to delivering high-quality results for our clients. Our commitment to innovation and excellence has made us a trusted partner in the industry, while our supportive work environment fosters career growth and employee satisfaction.