Clinical Research Coordinator — ALSA Research, Bridgeport, CT

Hands-on Clinical Research Coordinator position at an active Phase II–IV clinical research site in Bridgeport, CT. ALSA Research conducts industry-sponsored clinical trials across multiple therapeutic areas, and we are expanding our team.

We are looking for a CRC with prior clinical research experience who can step into an active study workload. You'll have direct interaction with trial participants in the conduct of study visits — including taking vital signs, drawing and processing blood samples, collecting patient data, and dispensing and administering study medication. The CRC supports, facilitates, and coordinates daily study activities including scheduling and performing patient visits, electronic source document creation/data entry, and coordinating monitoring visits.

This is a high-impact role with room to grow quickly at a site that values quality and initiative. Compensation based on experience. Bilingual (English and Spanish) a plus.

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 site SOPs.
• Regulatory Support – Assist with ICF management, IRB correspondence, and study binder updates.
• Specimen Handling – Process, package, and ship biospecimens per protocol and IATA regulations.
• 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.

Qualifications

Required:

• Prior experience as a Clinical Research Coordinator (minimum 1 year or multiple study cycles)
• Competency in phlebotomy (vacutainer & finger-stick)
• Familiarity with GCP, source documentation, and the conduct of study visits
• Authorization to work in the U.S. without sponsorship

Preferred:

• Experience with CTMS/EDC/eCRF platforms
• IATA certification or specimen handling experience
• Competency in intramuscular/subcutaneous injections
• ACRP (CCRC) or SOCRA (CCRP) certification
• Fluent in both English and Spanish
• Strong organizational skills with the ability to manage multiple studies simultaneously
• Excellent written & verbal communication and documentation review skills

Schedule & Compensation

• Hours: 32–40 hrs/week (typical schedule 8 AM – 4 PM, Monday–Thursday, often Fridays, rarely weekends). Predictable weekday schedule — no nights, rare weekends.
• Rate: $28 – $35 per hour (based on experience) + overtime if applicable
• Growth: Strong performers move up quickly — we invest in our team.

Benefits

• 401(k) with matching & company profit share
• Paid time off

Requirements

• Experience: Clinical Research: 1 year (Required)
• Commute: Bridgeport, CT 06606 (Required)
• Work Location: In person

Job Type: Full-time

Pay: $28.00 - $35.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Paid time off

Application Question(s):

• How many clinical studies have you worked on as a CRC?

Experience:

• Clinical Research: 1 year (Required)

Ability to Commute:

• Bridgeport, CT 06606 (Required)

Work Location: In person