Central Clinical Research Coordinator II
$75,000–$90,000 year
Remote
Job Summary
Hold end-to-end accountability for study success across the network, driving enrollment performance, data quality, and timely milestone achievement from activation through close-out. Monitor study health by reviewing enrollment metrics, screening data, and operational KPIs to proactively mitigate risks before they impact outcomes. Partner with site operations and central departments to standardize workflows, lead operational readiness assessments, and execute corrective actions for protocol deviations or enrollment challenges. Act as a network-level consultant traveling to sites to assess readiness for new studies, sponsor visits, and performance improvements. Serve as the primary liaison between Clinical Operations and Quality teams to support audit readiness and inspection preparation. Support business development initiatives by providing operational insights and enrollment projections during sponsor engagements. Lead the rollout of study updates and protocol amendments across all network sites while sharing best practices to promote standardization.
Required Qualifications
- Prior CRC (Clinical Research Coordinator) experience
- Bachelor's degree
- 2-3 years of experience in clinical research, project management, or clinical operations
- Strong understanding of clinical trial operations, including study execution, site workflows, participant management, regulatory compliance, GCP principle, and proficiency using EDC platforms
- Demonstrated experience managing sponsor relationships
- Proven ability to translate issue resolution plans into operational action, leading the execution and network-wide rollout of corrective measures with urgency and consistency
- Highly organized, metric-driven, and skilled at prioritizing competing demands across a complex, multi-study portfolio spanning multiple sites in a fast-paced environment
- Strong communication skills with the ability to escalate issues clearly, synthesize operational data, and propose practical solutions
- Willingness to travel to sites or conferences as needed to support readiness assessments and operational initiatives
Desired Qualifications
- site, CRO, or sponsor experience
- Proficiency with reporting tools, dashboards, and operational tracking systems
- Experience in neurology or psychiatry therapeutic areas
- Experience reviewing Clinical Trial Agreements
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.