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| Reference: |
2718 |
| Date Posted: |
4/21/2008 |
| Organization: |
Sterling-Hoffman Life Sciences |
| Employment Type: |
Full Time |
| Location: |
New Jersey, NJ |
Description:
Our client is a human health care company seeking innovative solutions in disease prevention, cure and care for the health and well being of people worldwide.
Job Responsibilities:
1) Plan, design and direct the Clinical Pharmacology Department studies in various therapeutic categories, under the supervision of the senior CPD staff
2) Work as a Study Director for assigned studies
3) Direct activities of monitors assigned to clinical studies with regard to protocol and CRF design, identification of qualified clinical investigators, negotiation of clinical study budgets, regular monitoring activities, verification of data, handling of clinical supplies as well as interacting with BCDM and PKMD
4) Develop (independently) long-range plans and budgets for the assigned studies, under the oversight of senior CPD staff
5) Ensure that all assigned studies are conducted as per GCPs, relevant SOPs and departmental WPDs
Job Requirements:
1) Doctoral-level (Pharm. D. or Ph. D.) degree
2) 5 years of experience in clinical research in the pharmaceutical industry
3) Understanding of clinical research methodology, including study design, protocol writing and CRF preparation
4) Knowledge of GCP and local regulatory requirements
5) Working knowledge of the IND/NDA process acquired through direct industrial experience
6) Good knowledge of medical, scientific and clinical research techniques in assigned therapeutic area
Applicants are encouraged to apply directly by going to: http://www.sterlinglifesciences.com/jobs/lifesciences-jobs-02718.html
Salary: $90k-$105k
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| Healthcare Field: |
Biotechnology |
| Category: |
Clinical Research Associate |
| SubCategory: |
None |
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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 |