Research Associate Position
This role requires a detail-oriented and organized individual to conduct on-site visits, verify investigator qualifications, and review medical records. Strong communication skills are essential to effectively communicate protocol deviations and site issues.
Responsibilities include:
* Conducting qualification, initiation, monitoring, and closeout visits;
* Verifying adequate investigator qualifications, training, and resources;
* Medical record and research source documentation verification;
* Communication with site staff regarding protocol deviations and entry errors;
* Assessing patient recruitment and retention success;
* Completion of monitoring reports and follow-up letters.
Qualifications
* Bachelor's degree in a relevant field;
* Prior experience as a study coordinator preferred;
* Excellent communication and organizational skills;
* Ability to work independently and efficiently;
* Willingness to travel up to 80% nationwide.
Our Organization
We are a leading contract research organization providing comprehensive clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate global medical innovation through scientific and disciplined approaches.