Remote Study Coordinator - Clinical Trials & Site Support

propharmagroup; United States; Hybrid; USD 52,000 - 76,000; Full time

Job summary

ProPharma Group is seeking a Central Study Coordinator to support remote site activities for assigned projects and must reside in or near High Point, NC. The role focuses on site communications, screening, recruitment, and protocol activities under the Principal Investigator's direction.

The position emphasizes data-entry, regulatory compliance, and collaboration with clinical teams, with a mix of remote and hybrid work options to accommodate in-person office time as needed.

Qualifications

• Bachelor's degree or equivalent experience with at least 2 years related experience.
• Experience with IRB/FDA policies.
• Strong communication and multitasking abilities.

Responsibilities

• Serve as point of contact for day-to-day Site communications, document submissions and activity coordination.
• Support pre-screening, screening and recruitment activities, as assigned.
• Responsible for subject re-consenting, acquiring medical records, conducting protocol activities, as directed by the Principal Investigator.
• Perform data-entry, evaluate and respond to system queries and monitor clinical databases as assigned.
• Establish and maintain timely Site communication as assigned.
• Maintain documentation which complies with IRB/FDA policies.
• Assist with study closeout.
• Assist site with other study-related activities as directed.
• Other duties as assigned.

Skills

Remote work

Communication

Independent work

Teamwork

GCP knowledge

Data entry

Multitasking

Privacy in remote work

Education

Bachelor's degree or equivalent

Job description

ProPharma Group is seeking a Central Study Coordinator to support remote site activities for assigned projects and must reside in or near High Point, NC. The role focuses on site communications, screening, recruitment, and protocol activities under the Principal Investigator's direction.

The position emphasizes data-entry, regulatory compliance, and collaboration with clinical teams, with a mix of remote and hybrid work options to accommodate in-person office time as needed.