Clinical Research Coordinator
alsaresearch
healthcare
research
Job Description:
Daily Responsibilities:
Participant Visits Perform check-ins, collect vitals, draw blood, administer investigational or placebo products, observe for AEs, and provide study-related education.
Study Documentation Complete source notes, CRFs/eCRFs, and maintain participant files in compliance with GCP and STC SOPs (training provided).
Regulatory Support Assist with ICF management, IRB correspondence, and study binder updates.
Specimen Handling Process, package, and ship biospecimens per protocol and IATA regulations (training provided if needed).
Scheduling & Tracking Coordinate participant appointments, follow-up calls, and data entry within CTMS/EDC systems.
Team Collaboration Work closely with the Principal Investigator, lead CRCs, and sponsor monitors to keep studies on time and audit-ready.
Job Requirements:
Required clinical background:
Prior experience as a Clinical Research Coordinator, Certified/Registered Medical Assistant or current LPN license (Connecticut)
Nice-to-have:
Prior exposure to or understanding of clinical trials and Good Clinical Practice (GCP), CTMS/eCRF platforms, IATA certification
Competency in phlebotomy (vacutainer & finger-stick) and intramuscular/subcutaneous injections
Excellent written & verbal communication, detail orientation, and EMR/computer proficiency. Excellent documentation review skills.
Strong organizational skills with the ability to manage multiple tasks simultaneously.
Ability to stand/walk for extended periods and lift up to 25 lbs (specimen coolers, study supplies)
Authorization to work in the U.S. without sponsorship
Fluent in both English and Spanish a plus
Compensation:
Schedule & Compensation
Hours: 32-40 hrs/week (typical schedule 8 am 4 pm, Monday - Thursday, often Fridays, rarely weekends); scheduling flexibility requirements can be discussed
Rate: $25 $35 per hour (depending on experience) + overtime if applicable
Benefits: 401k match, health insurance, HSA, paid time off
Job Location(s):
Stamford, Connecticut
Source:
Company Career Section
Competition:
N/A
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Sub-Investigator
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Principal Investigator
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ITT is moving from White Plains, New York, to Washington Blvd. in Stamford.
