Medix™
Clinical Research Coordinator - 234747
Medix™, Philadelphia, Pennsylvania, United States, 19124
Position Title:
Clinical Research Coordinator Location:
Philadelphia, Pennsylvania
A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible.
Summary: The Clinical Research Coordinator is responsible for coordinating and facilitating clinical research protocols across assigned sites. This role ensures protocol compliance, participant safety, and accurate data collection, while serving as a key liaison among investigators, sponsors, healthcare teams, and participants.
Responsibilities: Coordinate clinical research studies, including participant recruitment, screening, informed consent, and data collection. Collect, process, and ship research specimens in compliance with IATA guidelines. Monitor participant safety, adverse events, and protocol deviations. Support investigators during study initiation, monitoring, and close-out visits. Provide education and guidance to participants, families, and clinical staff regarding study procedures. Assist with regulatory submissions, quality assurance activities, and study documentation. Maintain accurate study records, data entry, and reporting to meet sponsor and regulatory requirements.
Qualifications: Education:
Bachelor’s degree required; advanced coursework or degree in a related field preferred. Experience:
Minimum 1 year in a clinical research setting (oncology experience preferred). Certifications:
CCRC, CCRP, or CCRA preferred (IATA certification required within 3 months of hire). Skills:
Strong organizational and communication skills; proficiency with Microsoft Office; knowledge of medical terminology; ability to manage multiple studies and deadlines.
Clinical Research Coordinator Location:
Philadelphia, Pennsylvania
A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as possible.
Summary: The Clinical Research Coordinator is responsible for coordinating and facilitating clinical research protocols across assigned sites. This role ensures protocol compliance, participant safety, and accurate data collection, while serving as a key liaison among investigators, sponsors, healthcare teams, and participants.
Responsibilities: Coordinate clinical research studies, including participant recruitment, screening, informed consent, and data collection. Collect, process, and ship research specimens in compliance with IATA guidelines. Monitor participant safety, adverse events, and protocol deviations. Support investigators during study initiation, monitoring, and close-out visits. Provide education and guidance to participants, families, and clinical staff regarding study procedures. Assist with regulatory submissions, quality assurance activities, and study documentation. Maintain accurate study records, data entry, and reporting to meet sponsor and regulatory requirements.
Qualifications: Education:
Bachelor’s degree required; advanced coursework or degree in a related field preferred. Experience:
Minimum 1 year in a clinical research setting (oncology experience preferred). Certifications:
CCRC, CCRP, or CCRA preferred (IATA certification required within 3 months of hire). Skills:
Strong organizational and communication skills; proficiency with Microsoft Office; knowledge of medical terminology; ability to manage multiple studies and deadlines.