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. No prior research experience required! This role is available as part time or full time.
Key Responsibilities
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. 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 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.
- 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.
- High school diploma required.
- Customer service or clinical experience required.
- Interest in developing clinical skills (vitals, blood draws, EKGs, etc.) required.