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Clinical Research Professional Jobs (NOW HIRING)

UAB

MANAGER-CLINICAL RESEARCH COORDINATION

Tampa, FL

$77K - $126K/yr

Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred. Preferences * Degree in Clinical Research, Public Health, etc.

Sentara

Clinical Research Coordinator

Norfolk, VA · On-site

$23.75 - $31.50/hr

Certified Clinical Research Professional (CCRP), Association of Clinical Research Professionals - Certified Professional (ACRP-CP) or Certified Clinical Research Professional (ACRP-CCRC) required ...

Sentara Healthcare

Clinical Research Coordinator

Norfolk, VA · On-site

$23.75 - $31.50/hr

Certified Clinical Research Professional (CCRP), Association of Clinical Research Professionals - Certified Professional (ACRP-CP) or Certified Clinical Research Professional (ACRP-CCRC) required ...

Headlands Research

Clinical Research Coordinator

Lake Worth, FL · On-site

$21.50 - $28.75/hr

JEM Research Institute | Full-Time Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high ...

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Clinical Research Professional information

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How much do clinical research professional jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for clinical research professional in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is a clinical research professional?

Clinical Research Professionals are specialists who design, conduct, monitor, and manage clinical trials that test the safety and effectiveness of medical treatments, drugs, and devices. They work in hospitals, research organizations, pharmaceutical companies, or academic institutions, ensuring that studies comply with regulatory requirements and ethical standards. Their roles may include coordinating trials, collecting and analyzing data, and ensuring the integrity and quality of research. Clinical Research Professionals play a crucial role in advancing medical knowledge and developing new therapies for patients.

What are the key skills and qualifications needed to thrive as a clinical research professional?

To thrive as a Clinical Research Professional, you need a solid understanding of clinical trial protocols, regulatory compliance, and scientific methodology, typically supported by a degree in life sciences or a related field. Familiarity with clinical data management systems, Good Clinical Practice (GCP) certification, and regulatory submission tools is often required. Strong attention to detail, effective communication, and organizational skills help ensure successful study coordination and data integrity. These competencies are crucial for maintaining compliance, protecting patient safety, and producing credible research outcomes.

What are typical challenges faced by clinical research professionals when managing multiple studies simultaneously?

Clinical Research Professionals often juggle several studies at once, which can present challenges such as time management, ensuring compliance with regulatory requirements, and maintaining clear communication among diverse teams. Balancing the differing timelines, protocols, and stakeholder expectations for each study requires strong organizational skills and attention to detail. Many professionals find success by leveraging project management tools, setting clear priorities, and fostering collaborative relationships with study coordinators, investigators, and sponsors.

What is the difference between Clinical Research Professional vs Clinical Research Coordinator?

AspectClinical Research ProfessionalClinical Research Coordinator
CredentialsOften requires a degree in health sciences, life sciences, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences or related fields; certifications like CCRP may be preferred
Work EnvironmentWorks in research institutions, pharmaceutical companies, or CROs, overseeing multiple studiesWorks directly with study participants, managing daily activities at clinical sites
Employer & Industry UsageUsed across research organizations, pharma, and biotech companiesPrimarily employed at clinical trial sites, hospitals, or clinics

While both roles are integral to clinical research, the Clinical Research Professional typically has broader oversight and may handle multiple projects, whereas the Clinical Research Coordinator focuses on managing individual studies at the site level.

What career paths are in clinical research?

Career paths in clinical research include roles such as Clinical Research Coordinator, Clinical Data Manager, Clinical Research Associate, and Project Manager. These positions often require knowledge of Good Clinical Practice (GCP), regulatory guidelines, and experience with clinical trial management systems. Advancement can lead to senior roles, specialized positions, or management opportunities within pharmaceutical, biotech, or healthcare organizations.

What do clinical research professionals do?

Clinical research professionals design, manage, and oversee clinical trials to evaluate the safety and effectiveness of new medical treatments or devices. They coordinate with research teams, ensure compliance with regulatory standards, and collect and analyze data using specialized software. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for this role.
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Clinical Research Professional jobs near you
Infographic showing various Clinical Research Professional job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, and 4% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Senior Clinical Research Coordinator

Austin, TX • On-site

Tekton Research Inc
Scientific Research and Development Services • 11 - 50 employees
Learn more about Tekton Research Incexternal

$24 - $32/hr

Full-time

Posted 29 days ago

Job description

Senior Clinical Research Coordinator - Austin, Texas

Full-Time/Non-Exempt/On-Site

Position Summary

The Senior Clinical Research Coordinator (Senior CRC) is an experienced clinical research professional responsible for managing multiple clinical trials from study start-up through close-out. This role ensures protocol compliance, participant safety, data integrity, regulatory compliance, and successful study execution.

The Senior CRC serves as a key liaison between investigators, sponsors, monitors, participants, and research staff while providing guidance and mentorship to junior coordinators. The ideal candidate is highly organized, proactive, detail-oriented, and able to effectively manage multiple priorities.

Key Responsibilities
  • Independently coordinate and manage multiple clinical trials from start-up through close-out.
  • Serve as a primary site contact for investigators, sponsors, monitors, vendors, and study teams.
  • Recruit, screen, consent, enroll, and retain study participants according to protocol requirements.
  • Conduct study visits and perform pediatric and adult phlebotomy and specimen processing as required.
  • Monitor participant safety and appropriately document and report adverse events and protocol deviations.
  • Maintain accurate source documentation, regulatory files, and essential study records in compliance with GCP, FDA regulations, and ICH guidelines.
  • Prepare and submit IRB and regulatory documents, including amendments and continuing reviews.
  • Maintain accurate study data in EDC and CTMS systems and resolve data queries within required timelines.
  • Prepare for and support monitoring visits, sponsor audits, and regulatory inspections.
  • Identify and resolve study issues proactively to maintain timelines, quality, and compliance.
  • Mentor and provide guidance to Clinical Research Coordinators and other research staff.
  • Contribute to process improvement and overall site quality and performance.
Required Qualifications
  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, Clinical Research, or related field preferred.
  • 3-5+ years of clinical research experience, with demonstrated ability to independently coordinate clinical trials.
  • Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical research processes.
  • Experience managing multiple clinical trials and competing priorities.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with EDC systems, CTMS, and Microsoft Office.
  • Strong organizational, problem-solving, and communication skills.
  • Ability to work independently, exercise sound judgment, and collaborate effectively with multidisciplinary teams.
  • Commitment to participant safety, data integrity, and research quality.
Preferred Qualifications
  • Current ACRP or CCRC, or equivalent certification.
  • Bachelor's or advanced degree in a healthcare, public health, or clinical research field.
  • Experience with industry-sponsored and/or multi-center clinical trials.
  • Experience mentoring junior research staff.
  • Experience supporting sponsor audits, regulatory inspections, or complex monitoring activities.
  • Experience with participant recruitment and retention strategies.
Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We value professional development, collaboration, accountability, and meaningful contributions.

If you're an experienced clinical research professional ready to take on greater responsibility and help lead high-quality clinical trial execution, we encourage you to apply and become part of the Tekton Research team.


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