Associate and Senior Directors, Project Manager Regulatory Affairs, office or homebased

MedCepts Medical Sales & Marketing Network - Medical Devices / Pharmaceuticals; Nashville (TN); On-site; USD 80,000 - 100,000; Full time

Job summary

MedCepts Medical Sales & Marketing Network in Nashville, Tennessee, is seeking qualified consultants to manage regulatory projects from start to finish. Candidates should have a degree in a life science discipline and at least 6 years of regulatory experience.

Responsibilities include acting as Project Manager, performing risk analysis, and providing strategic consultancy. Ideal candidates will possess advanced negotiating skills and the ability to adapt to challenges. Join us to make a difference in medical devices and pharmaceuticals.

Qualifications

• Minimum of 6 years of regulatory experience.
• Extensive experience in regulatory and/or technical writing.
• Ability to exercise independent judgment and propose mitigations.

Responsibilities

• Act as Project Manager involving regulatory or technical deliverables.
• Undertake risk analysis, management and contingency plans.
• Provide strategic regulatory consultancy on various projects.
• Perform various regulatory management assignments.

Skills

Regulatory experience

Technical writing

Negotiating and influencing skills

Independent judgment

Education

Degree in life science-related discipline

Job description

Overview

We are looking for qualified and experienced consultants to join our team to be independently and creatively instrumental in the groundwork of the project, from beginning to end. Qualified candidates will oversee and manage complex regulatory projects with the ability to ensure timely quality deliverables within allotted budget. Candidates must be able to ensure all assigned project work is completed in accordance with SOP's, policies and practices.

Responsibilities

• Act as Project Manager involving regulatory or technical deliverables
• Undertake risk analysis, management and contingency plans
• Provide strategic regulatory and/or technical consultancy on a variety of projects
• Perform various regulatory management assignments

Qualifications

• Degree in life science-related discipline with at least 6 years regulatory experience
• Extensive experience in regulatory and/or technical writing
• Advanced negotiating and influencing skills and the ability to identify and resolve issues, using flexible adaptable approach.
• Ability to exercise independent judgment, raise risks and propose mitigations