Clinical Research Coordinator
Competitive
You'll complete your application on the employer's website.
Competitive
You'll complete your application on the employer's website.
Job type
Salary
Competitive
Location
Sector
Posted
19 days ago
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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