Remote Clinical Study Coordinator (Argentina)

ProPharma; Raleigh (NC); Hybrid; USD 60,000 - 95,000; Full time

Benefits offered by this job

Remote work

Hybrid work

Diversity & inclusion

Job summary

ProPharma seeks a Central Study Coordinator to support remote site activities for assigned projects, based near Buenos Aires, Argentina. You will serve as the main contact for site communications, assist with screenings and recruitment, and handle medical records and protocol activities under the direction of the Principal Investigator.

Responsibilities include data-entry, responding to system queries, and ensuring IRB/FDA compliant documentation while maintaining effective site communication

Qualifications

• Bachelor’s degree or equivalent experience (minimum 2 years related, combined education, knowledge, and skills)
• Strong communication skills, verbal and written
• Ability to work independently and in a team
• Knowledge of ICH/GCP and applicable regulations and guidelines

Responsibilities

• Serve as point of contact for day-to-day site communications and document submissions.
• Support pre-screening, screening and recruitment activities.
• Re-consenting, acquiring medical records, conducting protocol activities as directed by the PI.
• Perform data-entry and monitor clinical databases.
• Maintain timely site communications and regulatory documentation; assist with study closeout.

Skills

Critical thinking

Communication

Independence

GCP knowledge

Education

Bachelor’s degree or equivalent

Job description

ProPharma seeks a Central Study Coordinator to support remote site activities for assigned projects, based near Buenos Aires, Argentina. You will serve as the main contact for site communications, assist with screenings and recruitment, and handle medical records and protocol activities under the direction of the Principal Investigator.

Responsibilities include data-entry, responding to system queries, and ensuring IRB/FDA compliant documentation while maintaining effective site communication