Study Coordinator

Study Coordinator - Phase II-IV Studies - Strong patient-facing and site coordination experienceUpsilon Global are seeking an experienced Study Coordinator for an active Phase II-IV clinical research site based in Bridgeport, CT. This is a hands-on role within a busy site environment and requires a CRC with strong patient-facing experience, organisational skills, and the ability to manage multiple ongoing studies.You'll be working closely with the Principal Investigator, site team, and sponsor monitors to ensure the smooth running of clinical trials, maintaining high-quality standards and keeping studies on track and audit-ready.This is a fantastic opportunity for someone with strong coordination skills and initiative to have a direct impact on study delivery and patient experience within a growing research site.Key information: Position: Study Coordinator Employment: Full-time FTE: 1.0 Indication: Multi-therapeutic (Phase II-IV studies) Location: Bridgeport, CT (on-site)Key duties: Participant visits including check-ins, vital signs, blood draws, and administration of investigational products Collection and documentation of patient data, including source notes and CRFs/eCRFs Scheduling and coordination of patient visits and follow-ups Support with study documentation and maintenance of participant files in line with GCP Assisting with regulatory activities including ICF management and IRB correspondence Processing, packaging, and shipment of biological samples per protocol and IATA guidelines Coordination of monitoring visits and ensuring audit readiness Collaboration with investigators, site staff, and sponsors to maintain study timelinesBackground and experience: Prior experience as a Study Coordinator or Clinical Research Coordinator (minimum 1 year or multiple study cycles) Strong understanding of GCP, source documentation, and study visit conduct Competency in phlebotomy (vacutainer and finger-stick) Experience with CTMS/EDC/eCRF systems beneficial Specimen handling experience and/or IATA certification advantageous Experience administering intramuscular or subcutaneous injections beneficial ACRP (CCRC) or SOCRA (CCRP) certification advantageous Fluency in English required; Spanish beneficial Strong organisational skills with the ability to manage multiple studies simultaneously Excellent communication and documentation review skillsThis role would be well suited to a proactive study nurse looking to grow within a high-performing clinical research site environment.For more details please apply directly or send your application to Jessie.Malinga@ or Juliana.Madiba@

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