Clinical Research Coordinator

Job Title: Clinical Research Coordinator

Location: Onsite - MA

Job Type: Contract

Job Summary

We are looking for a Clinical Research Coordinator to support the planning, coordination, and execution of clinical research studies. This role is ideal for individuals interested in clinical research and healthcare who want to gain experience in managing clinical trials while ensuring compliance with regulatory and ethical standards.

Responsibilities:

• Coordinate day-to-day clinical trial activities.
• Schedule participant visits and maintain study calendars.
• Assist with participant screening, enrollment, and informed consent.
• Collect, verify, and maintain clinical study data.
• Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
• Maintain regulatory binders and study documentation.
• Coordinate communication between investigators, sponsors, and study participants.
• Track study progress and prepare status reports.
• Support monitoring visits and regulatory audits.
• Assist with adverse event reporting and protocol documentation.
• Maintain confidentiality of patient information.

Required Qualifications:

• Bachelor's degree in Life Sciences, Healthcare, Nursing, Public Health, or a related field.
• 0–2 years of clinical research or healthcare experience.
• Knowledge of Good Clinical Practice (GCP) guidelines is preferred.
• Strong organizational, communication, and interpersonal skills.
• Ability to manage multiple tasks and meet deadlines.
• Proficiency in Microsoft Office applications.

Apply / Refer:

Abhiram

Recruiter | United Consulting Hub

Email: abhiram@unitedconsultinghub.com