Clinical Research Coordinator

Responsibilities

• Direct Clinical Research Operations across assigned protocols.
• Establish workflows, coordinate protocol-specific deliverables, and ensure studies execute in accordance with protocol requirements, regulatory standards, and organizational expectations.
• Manage Regulatory Compliance and Data Integrity.
• Direct preparation and submission of regulatory documentation.
• Oversight of safety reporting obligations.
• Implementation of corrective actions to maintain audit readiness.
• Lead Enrollment and Participant Engagement.
• Drive participant recruitment strategy.
• Optimize screening and enrollment workflows.
• Maintain study performance targets while ensuring positive participant experience and retention.
• Own and Direct External Research Partnerships.
• Serve as the primary point of contact for sponsors, investigators, and CROs.
• Drive study feasibility, site selection decisions, and resolution of operational issues.
• Support and Develop the Research Enterprise.
• Mentor research team members.
• Reinforce protocol standards across sites.
• Contribute to the operational growth and consistency of the broader research business unit.
• Lead Protocol Planning and Feasibility Assessments.
• Evaluate new study opportunities.
• Assess site capabilities and resource requirements.
• Provide strategic recommendations that inform protocol development and research program growth.

Qualifications

• Advanced knowledge of clinical research regulations, quality management principles, and documentation standards, with ability to interpret and apply requirements to maintain compliance and audit readiness.
• Demonstrated ability to exercise independent judgment in managing multiple studies, establishing priorities, and driving performance outcomes across research operations.
• Ability to analyze study performance metrics, identify improvement opportunities, and implement operational enhancements that impact enrollment, compliance, and data quality.
• Effective communication and interpersonal skills for interaction with sponsors, CROs, investigators, participants, and organizational leadership.

Required Education

• Bachelor's Degree

Other

• Professional certification through the Association of Clinical Research Professionals or Society of Clinical Research Associates preferred
• Minimum Years Related Experience: 4-6 Years