Clinical Research Coordinator III jobs in United States
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SRI · 1 day ago

Clinical Research Coordinator III

SRI is an independent nonprofit research institute dedicated to innovative solutions in biosciences, and they are seeking a Clinical Research Coordinator III to manage complex clinical research studies. The role involves participant recruitment, data management, and ensuring compliance with regulatory requirements while mentoring junior staff.

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Responsibilities

Actively participates in participant recruitment, screening, informed consent, and enrollment
Coordinates complex study visits and procedures in accordance with protocol requirements
Oversees accurate data collection, source documentation, and entry into EDC systems
Performs data cleaning and resolves queries within sponsor-required timelines
Collects, processes, labels, stores, and ships biospecimens per laboratory manual specifications
Monitors participant safety, clinical status, and adverse events; ensures timely reporting
Ensures compliance with ICH-GCP, FDA, OHRP, HIPAA, and sponsor requirements
Manages regulatory components of studies, including maintaining the electronic Investigator Site File (eISF)
Prepares for and participates in monitoring visits, SIVs, SQVs, and closeout visits
Provides mentorship and guidance to CRC I and CRC II team members
Participates in team meetings, investigator meetings, and sponsor-required trainings
Collaborates with investigators, clinicians, and research staff to support study execution
Assists in developing recruitment materials, source documents, and study tools
Maintains awareness of industry best practices and evolving research regulations

Qualification

Clinical trial experienceICH-GCP knowledgeBiospecimen handlingBLS certificationACLS certificationEDC systems proficiencyRegulatory submission experienceLeadership abilityOrganizational skillsProblem-solving skillsCommunication skillsInterpersonal skills

Required

Bachelor's degree in health science, medical, or related discipline
4–6 years of experience working with commercial clinical trials
BLS and/or ACLS certification
Proficiency with Microsoft Office and common EDC systems
Strong understanding of ICH-GCP, FDA, OHRP, and HIPAA regulations
Experience with biospecimen collection, processing, and shipping
Excellent organizational and problem-solving skills with ability to manage multiple studies
Strong communication and leadership ability
Ability to maintain strict confidentiality and data security
U.S. Citizenship or Permanent Residency required

Preferred

ACRP-CCRC or SOCRA certification
Extensive knowledge of medical terminology, clinical lab assessments, and pharmacovigilance
Experience with IRB processes and regulatory submission platforms (e.g., ePortal)

Benefits

SRI's Pay for Outstanding Performance program
Annual Performance Based Compensation program
Competitive benefits package

Company

An independent non-profit institute headquartered in Silicon Valley, SRI is a global leader in research and development.

Funding

Current Stage
Late Stage
Total Funding
$34M
Key Investors
Advanced Research Projects Agency for Health
2025-10-20Grant· $34M

Leadership Team

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David Parekh
Chief Executive Officer
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Peter Marcotullio
Sr. Vice President, Commercialization
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