|
Advertisement
Advertisement
|
| Reference: |
2723 |
| Date Posted: |
4/24/2008 |
| Organization: |
Sterling-Hoffman Life Sciences |
| Employment Type: |
Full Time |
| Location: |
Bethany Beach, DE |
Description:
Our client is a reputable, privately held CRO that is experiencing unprecedented growth. The company has an experienced management team, a very high customer retention rate, industry low employee turnover and a dedication to helping their staff maintain a strong work-life balance. This is a great opportunity for the right candidate!
Job Responsibilities:
1) Implement clinical studies, study monitoring, study management and data management/reporting
2) Act as an effective and efficient liaison between the study-site staff and company
3) Prepare regulatory reports and clinical documents
4) Create study management tools
5) Coordinate data collection/reporting with other departments
6) Assist with the development of junior staff and the initiative to participate in departmental programs
Job Requirements:
1) RN/BS degree in Biological Sciences or a related field (or equivalent combination of education and experience)
2) Minimum 5 years of CRA experience in monitoring clinical trials from qualification to closeout
3) Minimum 1.5 years experience in cardiovascular trials
4) In-depth knowledge and understanding of FDA regulations and GCPs
5) Excellent problem-solving skills
6) Exceptional interpersonal and communication skills
7) Willingness to travel – 65% (overnight)
Applicants are encouraged to apply directly by going to: http://www.sterlinglifesciences.com/jobs/lifesciences-jobs-02723.html
|
| Healthcare Field: |
Biotechnology |
| Category: |
Research Associate |
| SubCategory: |
None |
|
Job Posted By:
Similee Harvey
Sterling-Hoffman Life Sciences
800 West El Camino Real ,Suite 180
Mountain View
United States
94040
View more jobs posted by Similee Harvey |