Description
Qualifications:- Clinical research experience in the medical device industry
- Experince writing a clinical protocol
- Knowledge of medical device and clinical practice regulations and guidelines
- Microsoft Office
- Strong knowledge of biostatistics, trial design, and medical terminology
- Ability to effectively lead a team, and work effectively on cross functional teams
- Strong project management skills
- Strong written, oral, and interpersonal communication skills
If interested in this position, please reply with a copy of your updated resume in word format.
To find out more about Real please visit www.realstaffing.com