We are seeking Director of Project Management whom will provide Project Management to the current portfolio of projects, and work with contract manufacturers both in the US and abroad. Experience with Generics or CMO/CDMO is highly preferred.
This is a very hands-on role in a small department with a tremendous avenue for growth, you will be reporting into, and working directly with the companies Executive leadership.
This position will include a generous base salary, a 20% bonus, and stock options.
You will independently manage and coordinate complex drug development activities for cross functional development projects, including the project management of CMC, clinical and regulatory activities. You will also work across research, development and commercial departments to establish strategy and drive execution of drug development programs.
To qualify, you will bring a minimum of 5 years' experience in a Project Management function in either a generic or New Drug Pharmaceutical environment.
PMP Cerification is highly desired, but not required.
CMC experience is necessary.
Excellent understanding of the overall drug development process, including its various development phases, such as pre-clinical development, clinical development, regulatory development, and commercialization is an absolute must.
This role is onsite near Bridgewater, NJ.
