|
|
|
|
Associate Director / Director Regulatory Affairs Job
|
| Employer Name: PharmaceuticalCrossing |
SpiderID: 2350830 |
| Location: Columbia, Maryland |
Date Posted: 7/8/2008 |
| Wage: |
Category: Medical/Health |
| Job Code: 6136486 |
|
Job Description:
In this role, you will ensure timeliness of deliverables; edit/format/review regulatory documents; and work with staff in resolving regulatory issues and/or problems. Ensure that the company adheres to all applicable regulations. Additionally, you may serve as the team member for specific projects; be responsible for gathering and entering regulatory information related to specific projects; perform regulatory and/or quality assurance reviews of data or reports; attend project meetings, professional meetings, seminars and workshops; and document all phases of involvement in any specific project. The qualified candidate will have a bachelor's degree in the life sciences or equivalent, along with 10 years of experience in the pharmaceutical or CRO industry with at least 3 of these years as a regulatory affairs Manager or higher level. The candidate must be experienced in writing and compiling regulatory documents (i.e. (INDs, NDAs, BLAs, DMFs, FDA meeting packages, IBs, etc.), Hands-on strategic regulatory planning experience is preferred.
For more information, please click here to visit us at PharmaceuticalCrossing
For further information, please visit us online at http://www.pharmaceuticalcrossing.com
Sign Up Now
Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: PharmaceuticalCrossing |
|
|
|
| City: Pasadena |
|
| State: California |
|
| Zip: |
|
Web Site: http://www.pharmaceuticalcrossing.com
|
|
|
|
|
|
|