- Opportunity to continue or break into clinical research
- Be responsible for the success of various trials, working directly with the Principal Investigator/Physician
- Work with a small team = bigger influence on day-to-day
- Collaborating with the principal investigator to ensure the successful conduct of clinical trials
- Monitoring study participants and ensuring their safety and well-being
- Recording accurate and complete study data and maintaining study documentation
- Ensuring compliance with Good Clinical Practices (GCPs) and Standard Operating Procedures (SOPs)
- Communicating effectively with study participants, the sponsor, and the research team
- Providing support to the principal investigator with study-related activities
- Reviewing and maintaining study-related records, such as case report forms (CRFs)
- Participating in the resolution of study-related issues or adverse events
- Attending study-related meetings, training, and workshops
- Staying current with industry developments and regulatory requirements.
- Must be a licensed, certified Physician Assistant in the state of Illinois.
- Clinical research experience is highly preferred.
- Current experience as a Sub-Investigator is also highly preferred.
- Proficiency in procedures like EKG, phlebotomy, and injections/IVs.
- Ability to manage multiple tasks and prioritize responsibilities.
- Bilingual - Spanish Strongly preferred
Clinical Research Physician Assistant - North Chicago, United States - SQRL
Description
HIGHLIGHTS
THE COMPANY
Our client is a local clinical research company near Uptown Chicago that specializes in General Medicine clinical trials. Their goal is to serve the community and they are dedicated to providing the utmost quality care for their patients. They are looking to bring on a Clinical Research Physician Assistant (Sub-Investigator) to their team
THE ROLE
As a Clinical Research Physician Assistant (Sub-Investigator), you will play a key role in conducting clinical trials and ensuring their success by following Good Clinical Practices (GCPs) and the company's Standard Operating Procedures (SOPs). You will collaborate with the Principal Investigator, monitor study participants, and maintain accurate study documentation. This position requires strong organizational and communication skills, attention to detail, and a passion for medical research. You may also have the opportunity to pick up Clinical Research Coordinator responsibilities and gain a deeper knowledge of the Clinical Research realm.
RESPONSIBILITIES
REQUIREMENTS