Remote Clinical Research Assistant – Data & Site Coordination

ProPharma; Raleigh (NC); Hybrid; USD 44,000 - 60,000; Full time

Job summary

ProPharma in Raleigh, NC, is seeking a Research Assistant to support remote site activities for assigned projects, serving as the day-to-day site contact and coordinating documentation submissions.

The role requires handling data-entry, pre-screening support, and ensuring IRB/FDA compliant documentation, with the study team collaboration in a hybrid work setup. A Bachelor’s degree and research experience are preferred.

Qualifications

• Bachelor’s degree or equivalent experience (minimum 1 year related, combined education and skills).
• Research experience preferred.

Responsibilities

• Serve as point of contact for day-to-day Site communications, document submissions and activity coordination.
• Support pre-screening as assigned.
• 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

Strong communication skills

Independent worker

Critical thinking

Remote collaboration

Study team experience

Education

Bachelor's degree or equivalent experience

Job description

ProPharma in Raleigh, NC, is seeking a Research Assistant to support remote site activities for assigned projects, serving as the day-to-day site contact and coordinating documentation submissions.

The role requires handling data-entry, pre-screening support, and ensuring IRB/FDA compliant documentation, with the study team collaboration in a hybrid work setup. A Bachelor’s degree and research experience are preferred.