Clinical Research Coordinator 182825

Medix™; Springfield (MA); On-site; USD 41,328 - 48,216; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Job summary

A leading clinical research organization is seeking a Clinical Research Coordinator to oversee trial operations. This role involves coordinating activities from start-up to close-out, recruiting and managing study participants, and ensuring compliance with regulatory guidelines. Ideal candidates should have experience in clinical trials and strong organizational skills. Competitive compensation is offered, along with benefits including medical and vision insurance.

Qualifications

• Experience with clinical trial coordination and management.
• Knowledge of regulatory requirements and study protocols.

Responsibilities

• Coordinate and manage clinical trial activities from start-up to close-out.
• Recruit, screen, and consent study participants.
• Schedule study visits and collect data during each visit.
• Maintain accurate and complete study documentation.
• Ensure compliance with study protocols, IRB guidelines, and GCP.
• Handle investigational product (IP) per protocol if applicable.
• Communicate with sponsors, CROs, and regulatory bodies as needed.
• Support data entry and query resolution.

Job description

This range is provided by Medix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$30.00/hr - $35.00/hr

Direct message the job poster from Medix

We are seeking a Clinical Research Coordinator (CRC) to assist with the day-to-day operations of clinical trials. The CRC will work closely with investigators, sponsors, and study participants to ensure that trials are conducted according to regulatory requirements and study protocols.

Key Responsibilities:

• Coordinate and manage clinical trial activities from start-up to close-out
• Recruit, screen, and consent study participants
• Schedule study visits and collect data during each visit
• Maintain accurate and complete study documentation
• Ensure compliance with study protocols, IRB guidelines, and GCP
• Handle investigational product (IP) per protocol (if applicable)
• Communicate with sponsors, CROs, and regulatory bodies as needed
• Support data entry and query resolution

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Research Services

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

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