Clinical Research Coordinator

in Healthcare + Life Sciences
  • Reading, PA View on Map
  • Salary: $60,000.00 - $70,000.00
Permanent

Job Detail

  • Experience Level Entry Level
  • Degree Type Associate of Science (AS)
  • Employment Full Time
  • Working Type On Site
  • Job Reference 0000011108
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    Our client is a provider-led professionally managed organization where clinical decisions are made by those who understand patient care best. They offer work-life balance and growth opportunities while doing impactful work.

Job Description

Job Title: Clinical Research Coordinator

 

About the Role:

We are seeking a dedicated and experienced Clinical Research Coordinator to join our team. The ideal candidate will have patient-facing experience and at least 1 year of experience as a study coordinator in a clinical trial setting. Phlebotomy training/experience, laboratory sample processing experience, and ECG training are strongly preferred.

 

Responsibilities:

·        Coordinate and oversee clinical research studies in accordance with protocols and regulatory requirements.

·        Recruit, screen, and enroll eligible participants for studies.

·        Obtain informed consent from participants and maintain documentation.

·        Perform or assist with clinical procedures, such as phlebotomy, ECGs, and laboratory sample processing.

·        Collect, record, and maintain study data and source documents.

·        Communicate effectively with study sponsors, investigators, and study team members.

·        Ensure compliance with study protocols, regulations, and institutional policies.

·        Participate in study meetings, trainings, and audits as required.

Qualifications:

·        Bachelor's degree in a health-related field or equivalent experience.

·        Minimum of 1 year of experience as a study coordinator in a clinical trial setting.

·        Patient-facing experience/background is essential.

·        Phlebotomy training/experience is strongly preferred.

·        Laboratory sample processing experience is strongly preferred.

·        Trained to perform ECGs is strongly preferred.

·        Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

·        Excellent communication, organization, and interpersonal skills.

·        Ability to work independently and as part of a team.

·        Detail-oriented with strong problem-solving skills.

  • ShareAustin:

Related Jobs