Remote Clinical Study Coordinator

ProPharma; Raleigh (NC); Hybrid; USD 55,000 - 75,000; Full time

Job summary

ProPharma is seeking a Central Study Coordinator to coordinate and support remote site activities for assigned projects. You will reside in or near High Point, NC and support pre-screening, recruitment, consent, data entry and site communications.

The role requires a Bachelor’s degree with related experience and knowledge of ICH/GCP regulations. You will work to maintain regulatory documentation and assist with study closeout in a collaborative, compliant environment.

Qualifications

• Bachelor's degree or equivalent experience required.
• Experience coordinating clinical site activities.
• Knowledge of ICH/GCP guidelines and regulatory requirements.

Responsibilities

• Serve as point of contact for day-to-day site communications and document submissions.
• Support pre-screening, screening and recruitment activities as assigned.
• Responsible for subject re-consenting and acquiring medical records.
• Perform data-entry and monitor clinical databases as assigned.
• Maintain timely site communication and regulatory documentation.
• Assist with study closeout and other site-related tasks as directed.
• Collaborate with Principal Investigator and study team as needed.
• Maintain privacy and comply with SOPs and regulations.

Skills

Study coordination

Remote site coordination

ICH/GCP knowledge

Communication skills

Independent work

Education

Bachelor's degree

Job description

ProPharma is seeking a Central Study Coordinator to coordinate and support remote site activities for assigned projects. You will reside in or near High Point, NC and support pre-screening, recruitment, consent, data entry and site communications.

The role requires a Bachelor’s degree with related experience and knowledge of ICH/GCP regulations. You will work to maintain regulatory documentation and assist with study closeout in a collaborative, compliant environment.