Research Assistant, On-Site, Jefferson City, MO
IQVIA•Jefferson City, MO
•Onsite
About The Position
This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills.
Requirements
- High School Diploma or equivalent
Nice To Haves
- Bachelor's Degree
Responsibilities
- Develop strong working relationships and maintain effective communication with study team members
- Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office
- Assists with the screening, recruiting and enrollment of research subjects
- Perform patient/research participant scheduling
- Collect patient/research participant history
- Data entry and management
- Coordinate follow up care and laboratory procedures
- Adhere to an IRB approved protocol
- Assist in the informed consent process of research subjects
- Support the safety of research subjects
- Coordinate protocol related research procedures, study visits, and follow up care
- Comply with company and Sponsor policies, standard operating procedures (SOPs) and guidelines
- Schedule subject visits and procedures
Benefits
- health and welfare and/or other benefits
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Upload and Match Resume
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
