Clinical Research Assistant

Rovia Clinical Research; Anniston (AL); On-site; USD 38,000 - 54,000; Full time

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

Position Summary:

The Clinical Research Assistant is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success. No prior research experience required! This role is available as part time or full time.

Key Responsibilities:

• Conduct and coordinate patient visits in accordance with study protocols.
• Perform clinical tasks such as vital signs, ECGs, specimen collection/processing, and phlebotomy (as applicable).
• Ensure informed consent is properly obtained and documented.
• Educate and guide participants throughout the study, ensuring a positive patient experience.
• Monitor subject safety, report adverse events, and elevate concerns as appropriate.
• Complete timely and accurate source documentation and EDC data entry.
• Resolve data queries and ensure data integrity.
• Maintain investigational product accountability and proper storage/handling.
• Prepare for and support monitoring visits, audits, and inspections.
• Collaborate with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Perform other duties as assigned.

Skills/Abilities:

• Excellent organizational skills and attention to detail.
• Strong interpersonal and communication skills.
• Ability to multitask and manage competing priorities in a fast-paced environment.
• Proficiency in Microsoft Office applications.
• Ability to work both independently and collaboratively.
• High level of professionalism and commitment to patient confidentiality.

Education/Experience:

• High school diploma required.
• Customer service or clinical experience required.
• Interest in developing clinical skills (vitals, blood draws, EKGs, etc.) required.

Work Schedule:

Monday-Thursday 8:00AM-5:00PM, Friday 8:00AM-1:00PM, optional weekends/overnights