Clinical Study Coordinator

Proclinical is seeking a dedicated Clinical Study Coordinator. This role involves coordinating clinical research projects in compliance with federal regulations, providing technical support to Principal Investigators, and ensuring quality assurance measures are in place. The successful candidate will also be responsible for reporting adverse events to relevant authorities, coordinating external audits, and serving as a liaison between the institution and sponsor.

Key Responsibilities

• Coordinate clinical research projects in compliance with federal regulations.
• Provide technical support to Principal Investigators.
• Implement quality assurance measures to ensure compliance.
• Abstract medical information from various sources in the patient medical record.
• Report adverse events to medical monitor, FDA, and all other governing bodies.
• Coordinate all external audits and monitoring visits.
• Serve as a departmental and system-wide resource.

Requirements

• Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or a related field.
• Strong organizational, analytical, and problem-solving skills.
• Excellent verbal and written communication skills.
• Previous experience in a coordinator role is beneficial but not mandatory.
• Certifications such as SOCRA, ACRP, and IATA are preferred but not required.

If you are having difficulty in applying or if you have any questions, please contact Natalie Magola at n.magola@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.