A leading healthcare institution in California is seeking a full-time Quantitative Study Coordinator. The role entails managing regulatory compliance for clinical trials and population-based research, requiring strong analytical skills and effective communication. Ideal candidates will have experience in clinical research, be able to work under minimal supervision, and must be bilingual in English and Spanish. Flexibility and the ability to manage multiple projects are essential.
Qualifications
Proven experience as a Regulatory Coordinator in clinical trials.
Ability to prioritize workflow under minimal supervision.
Strong interpersonal and organizational skills.
Responsibilities
Serve as Regulatory Coordinator for various clinical trials.
Prepare, manage, and submit regulatory documents.
Interact effectively with study team and sponsors.
Skills
Clinical and population-based research experience
Strong analytical skills
Bilingual English / Spanish
Strong written communication skills
Strong computer skills
Tools
Microsoft Office Applications
Job description
A leading healthcare institution in California is seeking a full-time Quantitative Study Coordinator. The role entails managing regulatory compliance for clinical trials and population-based research, requiring strong analytical skills and effective communication. Ideal candidates will have experience in clinical research, be able to work under minimal supervision, and must be bilingual in English and Spanish. Flexibility and the ability to manage multiple projects are essential.