Job Summary
The position of Clinical Research Associate in Chicago, Illinois involves overseeing and guiding clinical studies at investigative sites. The role requires ensuring that all clinical trials are executed, documented, and communicated in accordance with the established protocol, standard operating procedures (SOPs), International Conference on Harmonisation of Good Clinical Practice (ICH-GCP), and other relevant regulations.
Responsibilities
- Oversee the implementation and progress of clinical trials.
- Ensure compliance with study protocols and regulatory standards.
- Maintain detailed records of clinical study activities.
- Collaborate with investigative sites to facilitate smooth operation of trials.
Qualifications
- A background in life sciences or a related field is typically required.
- Experience in clinical research and knowledge of regulatory guidelines is preferred.
- Strong organizational and communication skills are essential.
- Ability to work collaboratively in a team environment.
Upsilon Global provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
