What are the responsibilities and job description for the Clinical Research Assistant position at Rovia Clinical Research?
About Us
At Rovia Clinical Research, we’re on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you’re just starting out or looking for a new path, you’ll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.
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.
Key Responsibilities
20 - 24 USD per hour(Jacksonville - University)
At Rovia Clinical Research, we’re on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you’re just starting out or looking for a new path, you’ll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.
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.
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 escalate 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.
- Strong knowledge of medical terminology and clinical procedures.
- Understanding of ICH/GCP and regulatory requirements.
- Excellent organizational skills and attention to detail.
- Strong interpersonal and patient-facing communication skills.
- Ability to multitask and manage competing priorities in a fast-paced environment.
- Proficiency in Microsoft Office, EDC, and CTMS applications.
- Ability to work both independently and collaboratively.
- High level of professionalism and commitment to patient confidentiality.
- High school diploma required, bachelor’s degree in related field preferred.
- 0-1 years of clinical research experience.
- Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) required.
- Phlebotomy or Medical Assistant certification preferred.
20 - 24 USD per hour(Jacksonville - University)