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Clinical Research Coordinator

  • Clinical Research Coordinator job type Posted on: Oct 20, 2026
  • Clinical Research Coordinator experience level Preferred Primary Care Physicians
  • Clinical Research Coordinator employment type nan, Uttar Pradesh
  • Clinical Research Coordinator employment type Onsite
  • Clinical Research Coordinator salary Full-time

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Job Title :

Clinical Research Coordinator

Job Type :

Full-Time

Job Location :

nan Uttar Pradesh United States

Remote :

No

Jobcon Logo Job Description :

Preferred Primary Care Physicians, one of Pittsburgh's largest private physician practices, is looking for a full-time Clinical Research Coordinator. The CRC will be responsible for assisting with daily clinical research operations, implementation and conduct of multiple clinical trials and ensuring all research activities are coordinated in compliance with federal, state and local regulations. Excellent verbal and written communication skills and an ability to communicate with a diverse group of people in a clear and concise manner. Detail oriented and highly organized. Self-motivated with the ability to work effectively while managing multiple studies and projects. Promote a team approach with high standards of professionalism and productivity.Expected Routine ResponsibilitiesDay to day clinical research and operational oversight of the research office and the coordination with the physician's clinical office, in accordance with GCP guidelines and all federal, state and local regulations. Exhibits strong study management skills through organization, communication, problem solving, conflict resolution and leadership..Recruits and screens potential study participants and performs intake assessmentsCreates and/or maintains all documents and records related to the studyActs as a point of reference for study participants by answering questions and keeping them informed on the study progressManages the inventory of equipment and supplies related to the study and orders more as neededCollects specimens and inputs data and patient information into electronic systemsCreates reports on each study, including notes on protocols, workload, data collection, and moreExcellent written and verbal communication skillsSuperior organizational and time management skillsCapable of working independently with minimal supervision and also as part of a teamSkilled with standard computer programs including the MS Office suiteUnderstanding of medical terminology as well as standard clinical procedures and protocols

Jobcon Logo Position Details

Posted:

Oct 20, 2026

Reference Number:

10440_4366179171

Employment:

Full-time

City:

nan

Job Origin:

APPCAST_CPC

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Preferred Primary Care Physicians, one of Pittsburgh's largest private physician practices, is looking for a full-time Clinical Research Coordinator. The CRC will be responsible for assisting with daily clinical research operations, implementation and conduct of multiple clinical trials and ensuring all research activities are coordinated in compliance with federal, state and local regulations. Excellent verbal and written communication skills and an ability to communicate with a diverse group of people in a clear and concise manner. Detail oriented and highly organized. Self-motivated with the ability to work effectively while managing multiple studies and projects. Promote a team approach with high standards of professionalism and productivity.Expected Routine ResponsibilitiesDay to day clinical research and operational oversight of the research office and the coordination with the physician's clinical office, in accordance with GCP guidelines and all federal, state and local regulations. Exhibits strong study management skills through organization, communication, problem solving, conflict resolution and leadership..Recruits and screens potential study participants and performs intake assessmentsCreates and/or maintains all documents and records related to the studyActs as a point of reference for study participants by answering questions and keeping them informed on the study progressManages the inventory of equipment and supplies related to the study and orders more as neededCollects specimens and inputs data and patient information into electronic systemsCreates reports on each study, including notes on protocols, workload, data collection, and moreExcellent written and verbal communication skillsSuperior organizational and time management skillsCapable of working independently with minimal supervision and also as part of a teamSkilled with standard computer programs including the MS Office suiteUnderstanding of medical terminology as well as standard clinical procedures and protocols

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