What are the responsibilities and job description for the Clinical Research Coordinator 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 Coordinator (CRC) 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
55,000 - 65,000 USD per year(Jacksonville - LaVilla)
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 Coordinator (CRC) 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
- Conducts and coordinates patient visits in accordance with study protocols.
- Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
- Ensures informed consent is properly obtained and documented.
- Educates and guides participants through the study, ensuring a positive patient experience.
- Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
- Completes timely and accurate source documentation and EDC data entry.
- Resolves data queries and ensures data integrity.
- Maintains investigational product accountability and proper storage and handling.
- Prepares for and supports monitoring visits, audits, and inspections.
- Collaborates 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.
- 2 years of clinical research experience.
- Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.
55,000 - 65,000 USD per year(Jacksonville - LaVilla)