Clinical Research Coordinator Job at CRO Strategies, Bryn Mawr, PA

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  • CRO Strategies
  • Bryn Mawr, PA

Job Description

Role Description

This is a contract role for a Clinical Research Coordinator, located on-site in Bryn Mawr, Pennsylvania. The Clinical Research Coordinator will be responsible for managing the day-to-day clinical trial activities, obtaining informed consent from study participants, ensuring protocol adherence, conducting clinical research tasks, and managing clinical trial documentation.

Qualifications

  • Experience in obtaining Informed Consent and ensuring Protocol adherence
  • Strong background in Research, with a focus on Clinical Research Experience
  • Proficiency in managing Clinical Trials and related tasks
  • Excellent organizational and documentation skills
  • Ability to work collaboratively in an on-site environment
  • Knowledge of regulatory requirements and GCP (Good Clinical Practice) guidelines
  • Bachelor’s degree in a related field or equivalent experience

NOTE: This role will start at 20 hrs/week with ability to convert to full-time.

Job Tags

Full time, Contract work,

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