IAN BALDWIN
Clinical Research Coordinator II
Rochester, MN · i.baldwin@email.com · (555) 762-4413
Summary
Clinical research coordinator with 6 years managing Phase I-III oncology and cardiology trials from IRB submission through close-out. Recruited over 300 participants and maintained a zero major-finding audit record across 5 sponsor inspections.
Experience
Clinical Research Coordinator II · Mayo Clinic
2021 - Present
- Coordinate 6 concurrent Phase II/III oncology trials, managing IRB submissions and protocol amendments for each
- Recruited and consented 180+ participants over 3 years, exceeding enrollment targets by an average of 18%
- Maintained a zero major-finding record across 5 sponsor and FDA audits by enforcing strict source-document verification
- Serve as site contact for 4 sponsors, leading monthly monitoring visits in Medidata Rave
Clinical Research Coordinator I · Parexel International
2018 - 2021
- Managed regulatory documentation and CRF completion for 4 cardiology device trials across 2 sites
- Reduced query resolution time by 30% by implementing a weekly EDC discrepancy-review process
- Consented 120 participants and tracked eligibility screening logs for a 3-arm device trial
Clinical Research Assistant · Hennepin Healthcare Research Institute
2016 - 2018
- Prepared regulatory binders and delegation logs for 3 investigator-initiated studies under GCP
- Entered and verified data for 400+ study visits in REDCap, holding entry error rates below 1%
- Scheduled participant visits and shipped specimens for a 120-patient diabetes registry
Education
B.S. Biology — University of Minnesota · 2018
Skills
GCP, IRB Submissions, Informed Consent, Medidata Rave, REDCap, Adverse Event Reporting, Protocol Adherence, CTMS, Patient Recruitment, Regulatory Compliance, Source Document Verification
Certifications
Certified Clinical Research Coordinator (CCRC), ACRP
Certified Clinical Research Professional (CCRP), SOCRA




