Study Coordinator – Phase II–IV Studies – Strong patient-facing and site coordination experience
Upsilon 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 timelines
Background 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 skills
This 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@upsilonglobal.com or Juliana.Madiba@upsilonglobal.com