Description |
The Clinical Research Coordinator's primary responsibility is managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a study and study closure activities.
|
Requirements |
1. Associates degree or equivalent work related experience; BA/BS preferred.
2. 1 year experience in clinical research or health care field.
3. Understanding of medical terminology and clinical trials preferred.
4. Ability to obtain CRA/CRC certification in timely manner.
5. Skills required:
* Working knowledge of PCs and word processing and data management software
* Verbal and written communication
* Goal-oriented; self-directive
* Initiation, motivation, creativity
* Organizational and interpersonal
* Ability to actively participate as a team player
* Mentoring/training of new CRC's
When applying, please specify your source: LatPro.com
|
|
