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Clinical Research Coordinator Dubois

Clinical Research Coordinator

Full Time • Dubois
Benefits:
  • Dental insurance
  • Health insurance
  • Vision insurance
  • Competitive salary
The Clinical Research Coordinator (CRC) is responsible for the day-to-day operations of clinical trials, ensuring compliance with protocols, regulations, and ethical standards. The CRC will manage participant recruitment, data collection, and documentation, while also maintaining the safety and well-being of study participants. 


Key Responsibilities:
  • Recruiting and enrolling eligible participants, obtaining informed consent, and ensuring participant safety throughout the study. 
  • Gathering, organizing, and managing clinical data, including case report forms, adverse event reports, and other study documentation. 

Protocol Adherence:
Ensuring the study is conducted according to the protocol, applicable regulations (like Good Clinical Practice (GCP), FDA guidelines), and Institutional Review Board (IRB) requirements. 


Study Operations:
Scheduling appointments, coordinating procedures, and maintaining study timelines. 


Communication and Collaboration:
Communicating effectively with participants, investigators, and other research team members. 


Quality Control:
Maintaining accurate records, managing study supplies, and ensuring adherence to protocols and procedures. 


Example Duties (may vary depending on the specific study)
Reviewing study protocols and preparing study materials.
Screening potential participants for eligibility.
Administering questionnaires and surveys.
Performing specific protocol procedures (e.g., taking vital signs, administering medications).
Collecting and processing clinical data.
Monitoring participant health and adverse reactions.
Documenting adverse events and reporting them to the appropriate authorities.
Assisting with data analysis and preparing reports.
Participating in study close-out activities.
Maintaining accurate and organized study records.

LOCATED IN PENNSYLVANIA, THIS IS AN ON-SITE POSITION AND REQUIRES IN PERSON INTERACTION WITH STAFF AND STUDY PARTICIPANTS
Compensation: $55,000.00 - $65,000.00 per year

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.





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U.S. Equal Opportunity Employment Information (Completion is voluntary)

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

You are being given the opportunity to provide the following information in order to help us comply with federal and state Equal Employment Opportunity/Affirmative Action record keeping, reporting, and other legal requirements.

Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiring process or thereafter. Any information that you do provide will be recorded and maintained in a confidential file.