Clinical Research Assistant
St. Augustine, Florida, United States · Tempo pieno
Sii il primo a candidarti
- Esperienza
- Fino a 1 anno
- Stipendio
- USD 20 – USD 23 / hour
- Aperture
- 1
- Pubblicato
- 3 settimane fa
- Modalità di lavoro
- In ufficio
- Istruzione
- High school diploma required, bachelor's degree in related field preferred
- Requisiti di ammissibilità
- <ul><li>Individuals with a high school diploma are eligible; a bachelor's degree in a related field is preferred.</li><li>Candidates with 0-1 years of clinical research experience are encouraged to apply.</li><li>Prior experience with patient-facing tasks such as phlebotomy, vital signs, and EKGs i…
- Riprendere
- È necessario candidarsi
Dove lavorerai
Descrizione del lavoro
About Us
Rovia Clinical Research is dedicated to advancing healthcare by bringing innovative treatments to local patient communities. We foster a supportive and valued work environment where employees can grow their careers and make a tangible impact. Our team operates under core values of People First, Humility, Integrity, One Team, and Results Accountability.
Position Summary
The Clinical Research Assistant plays a crucial role in coordinating and executing clinical trials, ensuring strict adherence to study protocols, ICH/GCP guidelines, sponsor expectations, and Rovia's Standard Operating Procedures. This position involves close collaboration with site teams to facilitate study startup, manage patient enrollment, maintain data quality, and contribute to the overall success of the trials.
Key Responsibilities
- Coordinate and conduct patient visits according to established study protocols.
- Perform essential clinical tasks, including taking vital signs, performing ECGs, processing specimens, and phlebotomy as needed.
- Ensure that informed consent is obtained correctly and thoroughly documented.
- Provide guidance and education to participants throughout their study journey, prioritizing a positive patient experience.
- Monitor participant safety diligently, report any adverse events, and escalate critical concerns promptly.
- Maintain accurate and up-to-date source documentation and enter data into Electronic Data Capture (EDC) systems in a timely manner.
- Address and resolve data queries to ensure the integrity and accuracy of study information.
- Manage investigational product inventory, including proper storage and handling procedures.
- Prepare for and actively support monitoring visits, audits, and regulatory inspections.
- Work collaboratively with site staff and investigators to uphold protocol adherence and optimize patient visit efficiency.
- Undertake other assigned duties as required to support study operations.
Skills and Abilities
- Possess a strong command of medical terminology and clinical procedures.
- Demonstrate a solid understanding of ICH/GCP and relevant regulatory requirements.
- Exhibit exceptional organizational skills with meticulous attention to detail.
- Communicate effectively with patients and colleagues, demonstrating strong interpersonal skills.
- Effectively manage multiple tasks and competing priorities in a dynamic, fast-paced setting.
- Proficient in using Microsoft Office Suite, EDC systems, and Clinical Trial Management Systems (CTMS).
- Capable of working autonomously and as part of a team.
- Maintain a high level of professionalism and a strong commitment to patient confidentiality.
Education and Experience
- A high school diploma is mandatory; a bachelor's degree in a relevant field is preferred.
- Possess 0 to 1 year of experience in clinical research.
- Required experience in patient-facing activities such as phlebotomy, vital signs monitoring, and ECGs.
- Phlebotomy or Medical Assistant certification is advantageous.
Additional Information
The hourly pay range for this position in St. Augustine is $20 to $23 USD.