Clinical Research Coordinator

in Pharma
  • Reading, PA View on Map
  • Salary: $60,000.00 - $70,000.00
Permanent

Job Detail

  • Experience Level Mid Level
  • Degree Type Bachelor of Science (BS)
  • Employment Full Time
  • Working Type On Site
  • Job Reference 0000009324
  • 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.

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  • This sponsor is committed to scientific excellence and innovation. They invest significantly in research and development to discover new treatments and improve existing ones. They focus on developing treatments that address unmet medical needs.