Clinical Research Coordinator

IQVIA

Medford, MAPart-timePosted Apr 12, 2026

Behavioral Health Market Context

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Job Description

ommunity, and ensuring compliance with the highest standards of patient care.

Key Responsibilities
• Conduct intricate clinical procedures, including ECG, spirometry, sample collection, and assessing vital signs.
• Perform phlebotomy to facilitate sample collection as required.
• Coordinate clinical research studies while adhering to study protocols and Good Clinical Practice (GCP) guidelines.
• Engage with patients by conducting consenting and study visits according to established protocols.
• Process laboratory samples and conduct ambulatory blood pressure monitor (ABPM) procedures.
• Support study execution by preparing necessary materials, setting up equipment, and managing logistical details.
• Recruit, screen, and orient volunteers, ensuring their comfort and safety throughout the study.
• Collect and accurately document clinical data in case report forms (CRFs); ensure timely and precise data entry.
• Collaborate with investigators and monitors, addressing inquiries and maintaining data quality.
• Act as an advocate for volunteers, ensuring a safe environment in line with Health and Safety policies.

Qualifications
• High School Diploma or equivalent education and experience.
• At least 1 year of relevant experience in clinical research is preferred.
• Familiarity with clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to build effective working relationships.
• Capability to assist in patient recruitment efforts, including phone prescreening and chart review.
• Aptitude for assisting with data entry and query resolution.
• Willingness to support patient visits effectively.

Please note: This position is not eligible for sponsorship.

This role is based in Malden, MA. Become part of a leading global provider of clinical research services that accelerates the development of innovative medical treatments, and help enhance patient outcomes and population health worldwide.

Compensation: The potential base pay range for this role is $35.00 to $42.00 per hour, with actual pay depending on various factors, including qualifications, experience, and location.

Qualifications

  • High School Diploma or equivalent education and experience
  • Familiarity with clinical trials, GCP principles, and medical terminology
  • Strong attention to detail and ability to build effective working relationships
  • Capability to assist in patient recruitment efforts, including phone prescreening and chart review
  • Aptitude for assisting with data entry and query resolution
  • Willingness to support patient visits effectively

Benefits

  • Compensation: The potential base pay range for this role is $35.00 to $42.00 per hour, with actual pay depending on various factors, including qualifications, experience, and location

Responsibilities

  • Schedule: Part-time, 24 hours per week
  • Join our dynamic team as a Clinical Research Coordinator (CRC) where you will play a vital role in supporting groundbreaking clinical research studies alongside an experienced principal investigator
  • This hands-on position involves performing critical clinical procedures, engaging with the community, and ensuring compliance with the highest standards of patient care
  • Conduct intricate clinical procedures, including ECG, spirometry, sample collection, and assessing vital signs
  • Perform phlebotomy to facilitate sample collection as required
  • Coordinate clinical research studies while adhering to study protocols and Good Clinical Practice (GCP) guidelines
  • Engage with patients by conducting consenting and study visits according to established protocols
  • Process laboratory samples and conduct ambulatory blood pressure monitor (ABPM) procedures
  • Support study execution by preparing necessary materials, setting up equipment, and managing logistical details
  • Recruit, screen, and orient volunteers, ensuring their comfort and safety throughout the study
  • Collect and accurately document clinical data in case report forms (CRFs); ensure timely and precise data entry
  • Collaborate with investigators and monitors, addressing inquiries and maintaining data quality
  • Act as an advocate for volunteers, ensuring a safe environment in line with Health and Safety policies


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