Research Assistant Job Opportunity
We are seeking a highly motivated and dedicated individual to join our team at RIO Clinical Trials as a Research Assistant, where you will have the opportunity to contribute significantly to the execution of clinical trial activities, adhering to all relevant regulations and guidelines. This role offers the chance to work closely with a dynamic team and directly impact the success of clinical research. Ideal candidates will possess strong analytical thinking, excellent prioritization abilities, adaptability in a fast-paced environment, and outstanding interpersonal and teamwork skills.
Key Responsibilities:
- Foster collaborative and effective working relationships with study team members, ensuring open communication and a positive working environment.
- Build and maintain strong partnerships with investigators and clinic staff, creating a foundation of trust and mutual respect.
- Assist in the screening, recruitment, and enrollment processes for research participants.
- Coordinate and schedule appointments for research participants in a timely and efficient manner.
- Gather and record comprehensive participant medical histories.
- Collect vital signs, including blood pressure, temperature, and EKG, as part of routine participant assessments.
- Perform or assist with blood draws, with the opportunity to learn and refine these skills if not already experienced.
- Manage and enter research data accurately, ensuring high-quality and reliable records.
- Coordinate follow-up care and necessary laboratory procedures for research participants.
- Ensure all activities comply with IRB-approved protocols.
- Support the informed consent process for participants, ensuring they are well-informed about the study.
- Prioritize and ensure the safety and well-being of all research subjects throughout their participation.
- Manage and coordinate study visits, research procedures, and follow-up care, in alignment with study protocols.
- Adhere to company, clinic, and sponsor policies, as well as standard operating procedures (SOPs) and guidelines.
- Schedule participant visits and associated procedures in a timely and efficient manner.
Required Knowledge, Skills, and Abilities:
- Pediatric phlebotomy experience is preferred.
- Willingness to perform blood draws or the ability to learn these techniques.
- Proficient understanding and ability to apply Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and relevant regulatory frameworks.
- Strong attention to detail, excellent interpersonal communication, and a proactive approach to problem-solving.
- Demonstrated expertise in using Microsoft Office software (Outlook, Word, Excel, PowerPoint, SharePoint) and clinical trial master file systems.
- Strong organizational and time management skills, with the ability to effectively handle multiple priorities.
This is an exciting opportunity for those looking to grow within the clinical research field and contribute to meaningful projects that advance medical knowledge. We also encourage medical assistants to apply, as while the role differs, it offers similar responsibilities and can provide substantial opportunities for career growth.
Job Type: Full-time
Pay: $22.00 - $24.00 per hour
Benefits:
- Free parking
- Paid time off
Medical Specialty:
- Cardiology
- Infectious Disease
- Public Health
Physical Setting:
- Clinic
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: In person
