Contract
Posted Sep 22, 2026
25–36 an hour
Job Description
Contracted Clinical Research Coordinator Role - Plymouth Meeting, PA (19462)
Key Responsibilities
• Protocol Execution: Perform protocol-driven patient visits and clinical procedures, including phlebotomy, IV administration, injections, vital signs, and ECG/EKGs.
• Data & Documentation: Maintain complete, audit-ready source documentation and accurately record study data into eCRF/EDC platforms in accordance with GCP standards.
• Informed Consent & Recruitment: Lead the informed consent process following FDA, IRB, and GCP guidelines. Actively and ethically recruit qualified participants to achieve enrollment goals.
• Safety & Regulatory Reporting: Promptly report Adverse Events (AEs) and submit Serious Adverse Events (SAEs) to sponsors within 24 hours while notifying the Principal Investigator (PI) and leadership.
• Trial Logistics: Monitor and maintain study supplies, investigational product inventory, and lab materials to ensure full availability for scheduled visits.
• Communication & Compliance: Serve as a primary liaison between site leadership, PIs/Sub-Is, CROs, sponsors, and trial participants while strictly maintaining HIPAA confidentiality.
Candidate Qualifications
• Experience: Minimum of 2 years of clinical research experience required, with direct background in oncology clinical trials.
• Clinical Skills: Hands-on competency in phlebotomy, IV placement, injections, ECGs, and vital sign collection highly preferred.
• Regulatory Knowledge: Strong working knowledge of GCP, ICH, FDA guidelines, and medical terminology.
• Technical Skills: Experience with electronic source platforms (e-Source/eCRF) and proficiency in Microsoft Office Suite.
• Core Competencies: Outstanding organizational skills, critical thinking abilities, high ethical standards, and excellent interpersonal skills to collaborate with investigators, sponsors, and study participants.
• Education: Bachelor’s degree preferred, but equivalent clinical research experience will be considered.
Additional Details:
• Position: Clinical Research Coordinator
• Location: Plymouth Meeting, PA (19462)
• Employment: ~6-12 Month Contract Role
• Hours: Monday-Friday; Onsite 5 Days a Week; 9AM-5PM
• Pay Rate: $25/hr-$36/hr (Dependent on background and years of experience)
Key Responsibilities
• Protocol Execution: Perform protocol-driven patient visits and clinical procedures, including phlebotomy, IV administration, injections, vital signs, and ECG/EKGs.
• Data & Documentation: Maintain complete, audit-ready source documentation and accurately record study data into eCRF/EDC platforms in accordance with GCP standards.
• Informed Consent & Recruitment: Lead the informed consent process following FDA, IRB, and GCP guidelines. Actively and ethically recruit qualified participants to achieve enrollment goals.
• Safety & Regulatory Reporting: Promptly report Adverse Events (AEs) and submit Serious Adverse Events (SAEs) to sponsors within 24 hours while notifying the Principal Investigator (PI) and leadership.
• Trial Logistics: Monitor and maintain study supplies, investigational product inventory, and lab materials to ensure full availability for scheduled visits.
• Communication & Compliance: Serve as a primary liaison between site leadership, PIs/Sub-Is, CROs, sponsors, and trial participants while strictly maintaining HIPAA confidentiality.
Candidate Qualifications
• Experience: Minimum of 2 years of clinical research experience required, with direct background in oncology clinical trials.
• Clinical Skills: Hands-on competency in phlebotomy, IV placement, injections, ECGs, and vital sign collection highly preferred.
• Regulatory Knowledge: Strong working knowledge of GCP, ICH, FDA guidelines, and medical terminology.
• Technical Skills: Experience with electronic source platforms (e-Source/eCRF) and proficiency in Microsoft Office Suite.
• Core Competencies: Outstanding organizational skills, critical thinking abilities, high ethical standards, and excellent interpersonal skills to collaborate with investigators, sponsors, and study participants.
• Education: Bachelor’s degree preferred, but equivalent clinical research experience will be considered.
Additional Details:
• Position: Clinical Research Coordinator
• Location: Plymouth Meeting, PA (19462)
• Employment: ~6-12 Month Contract Role
• Hours: Monday-Friday; Onsite 5 Days a Week; 9AM-5PM
• Pay Rate: $25/hr-$36/hr (Dependent on background and years of experience)
Additional Details
- City
- Plymouth Meeting
- State
- Pennsylvania
- Country
- US
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