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Full-time

Clinical Research Coordinator

Competitive

Oklahoma City, OKScience & PharmaceuticalPosted 19d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

Competitive

Posted

19 days ago

Job description

Tekton Research is a clinical research organization focused on conducting high-quality clinical trials that advance medical knowledge and improve patient care. The Clinical Research Coordinator will coordinate and manage clinical trials, recruit and support participants, maintain regulatory and study documentation, monitor safety, and ensure compliance with protocols and applicable regulations.

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

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

Preferred

Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred

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

Nursing Degree

Biology Degree

Health Sciences Degree

Public Health Degree

Advanced Nursing Degree

Advanced Public Health Degree

Clinical Research Degree

Clinical Trial Experience

Industry-Sponsored Trials

Multi-Center Clinical Trials

Clinical Monitoring

Participant Recruitment

Retention Strategies

Benefits

Competitive compensation

Comprehensive benefits

Opportunities for professional growth

Professional development is encouraged

Collaborative culture

Company

Multi-specialty clinical research site organization conducting Phase 1-4 trials

Austin, Texas, USA

https://tektonresearch.com/

Founded in 2006

51-200 employees

Qualifications

High school diploma or GED required

Minimum of six months to one (1) year of Clinical Research Coordinator experience

Working knowledge of Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and clinical research processes

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

Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred

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

Minimum of six months to one (1) year of Clinical Research Coordinator experience.

Required skills

Clinical Research Coordination, Clinical Practice (GCP), FDA Regulations, ICH Guidelines, Clinical Research Processes, Phlebotomy, Specimen Processing, Regulatory Documentation, Source Documentation, Electronic Data Capture (EDC) Systems, Microsoft Office, Clinical Trial Management Systems (CTMS)

Preferred skills

Verbal and Written Communication

Experience

1+ years

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