Entry-Level Clinical Trial Coordinator

Rovia Clinical Research

Anniston (AL)

On-site

USD 38,000 - 54,000

Full time

14 days+

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Job summary

Rovia Clinical Research is seeking a Clinical Research Assistant to coordinate and support clinical trials in line with ICH/GCP and sponsor requirements. The role collaborates with site teams to support startup, enrollment, data quality, and trial success. No prior research experience is required.

This position is available as part time or full time, on-site in Alabama. The successful candidate will assist with patient visits, vitals, and data entry while ensuring patient confidentiality and

Qualifications

  • High school diploma required.
  • Customer service or clinical experience required.
  • Interest in developing clinical skills (vitals, blood draws, EKGs, etc.) required.
  • No prior research experience required.

Responsibilities

  • Coordinate patient visits per study protocols.
  • Perform clinical tasks such as vitals, ECGs, and phlebotomy as applicable.
  • Ensure informed consent is properly obtained and documented.
  • Educate and guide participants to ensure a positive patient experience.
  • Monitor subject safety and report adverse events appropriately.
  • Complete source documentation and EDC data entry.
  • Resolve data queries and maintain data integrity.
  • Maintain investigational product accountability and storage/handling.
  • Support monitoring visits, audits, and inspections.
  • Collaborate with site staff to ensure protocol adherence and efficient visit flow.
  • Perform other duties as assigned.

Skills

Organizational skills
Interpersonal communication
Multitasking
Microsoft Office
Independent work

Education

High school diploma
Customer service experience
Clinical experience

Tools

Microsoft Office

Job description

Rovia Clinical Research is seeking a Clinical Research Assistant to coordinate and support clinical trials in line with ICH/GCP and sponsor requirements. The role collaborates with site teams to support startup, enrollment, data quality, and trial success. No prior research experience is required.

This position is available as part time or full time, on-site in Alabama. The successful candidate will assist with patient visits, vitals, and data entry while ensuring patient confidentiality and

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