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Clinical Research Coordinator

Tekton Research Inc·Richmond, Virginia

Full Time·On Site·2-5 yrs·Posted 1 day ago
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About the role

The Clinical Research Coordinator manages the day-to-day operations of clinical trials, ensuring compliance with protocols and regulatory standards. They serve as the primary liaison between stakeholders while performing clinical tasks like phlebotomy and maintaining accurate study documentation.

Clinical Research Coordinator (CRC)

About Tekton Research

Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance medical knowledge and improve patient care. We are a collaborative, values-driven team that believes in Focus, Discipline, and Accountability. At Tekton Research, we take pride in doing excellent work while fulfilling our mission of Making Life Better.

We offer competitive compensation, comprehensive benefits, and opportunities for professional growth in a supportive and fast-paced research environment.

Position Summary

The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical research studies, ensuring compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. The CRC serves as the primary liaison between investigators, sponsors, study participants, and regulatory agencies while ensuring participant safety, data integrity, and successful study execution.

This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple clinical trials simultaneously in a dynamic environment.

Key Responsibilities

  • Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.
  • Recruit, screen, consent, and schedule study participants according to protocol requirements.
  • Perform pediatric and adult phlebotomy, including blood collection for pediatric participants from newborn through 17 years of age, using age-appropriate techniques while ensuring patient comfort and safety.
  • Collect, process, package, and ship laboratory specimens according to protocol and sponsor requirements.
  • Maintain accurate source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and institutional policies.
  • Monitor participant safety and promptly identify, document, and report adverse events.
  • Prepare and submit regulatory documents, including Institutional Review Board (IRB) submissions, continuing reviews, and protocol amendments.
  • Collaborate with investigators, sponsors, monitors, and study staff to ensure successful study conduct.
  • Assist with monitoring visits, sponsor audits, and regulatory inspections.
  • Utilize Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS) to maintain accurate study data.
  • Ensure protocol compliance while maintaining the highest standards of participant care and research integrity.

Required Qualifications

  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.
  • Minimum of one (1) year of Clinical Research Coordinator experience.
  • Working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and clinical research processes.
  • Required experience performing pediatric phlebotomy on patients from birth through 17 years of age, including infants, children, and adolescents. Candidates must demonstrate proficiency in obtaining blood specimens safely while delivering compassionate, age-appropriate care.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Strong organizational and time management skills with the ability to prioritize multiple studies.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with Electronic Data Capture (EDC) systems and Microsoft Office applications.
  • Excellent verbal and written communication skills.
  • Ability to work independently while collaborating effectively with multidisciplinary teams.

Preferred Qualifications

  • Current ACRP-CRC or SOCRA certification.
  • Advanced degree in Nursing, Public Health, Clinical Research, or a related healthcare field.
  • Experience working on industry-sponsored or multi-center clinical trials.
  • Familiarity with clinical monitoring, 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 foster a collaborative culture where professional development is encouraged, contributions are valued, and every team member plays an important role in advancing healthcare.

If you are passionate about clinical research and committed to providing exceptional patient care, we encourage you to apply and become part of the Tekton Research team.

Requirements

Candidates must have at least one year of clinical research experience and proficiency in pediatric and adult phlebotomy. A high school diploma is required, with a bachelor's degree in a health-related field preferred.

  • high school
  • bachelor degree
  • Communication skills
  • Time management
  • Regulatory compliance
  • Specimen processing
  • Data integrity
  • Microsoft office
  • Informed consent
  • Clinical research coordination
  • Adverse event reporting
  • Good clinical practice
  • Participant recruitment
  • Electronic data capture
  • Pediatric phlebotomy
  • Clinical trial management systems
  • Adult phlebotomy

Benefits

  • Comprehensive benefits
  • Competitive compensation
  • Professional growth opportunities

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Location
Richmond, Virginia
Posted
Jul 28, 2026
Application
Employer website
TR

Hiring organization

Tekton Research Inc

Founded in 2006, Tekton Research is a multi-specialty clinical research site organization conducting Phase 1-4 clinical trials across neurology and psychiatry, cardiometabolic medicine, general medicine, infectious disease, pediatrics, and other high-need therapeutic areas....

IndustryResearch Services
TypePrivately Held
Size51-200 employees
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Market context

Virginia clinical research roles are selective

In Virginia, Clinical Research Coordinator roles are often competitive because employers look for candidates who can manage study compliance, documentation, and coordination across research teams. This posting requires U.S. citizenship, eligibility for Secret Clearance, a bachelor’s degree, and either recent CRC experience or current relevant certification, plus monitoring experience. Review the original job description carefully and align your resume to the clearance, research, and monitoring requirements; the job requirements and benefits here are AI-summarized from the source posting, which can save you research time.

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