Description:
Our client is currently seeking a Director level candidate to join their team.
Job requirements:
The candidate will be a self-starter and provide regulatory oversight for assigned products, in order to optimize and obtain shortest time to approval by regulatory agencies
Independently interacts with the Worldwide Regulatory Agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more of our Company’s investigational and marketed drugs/biologics
Additional Skills & Qualifications:
Bachelors Degree is a must
6-10+ years experience in regulatory settings
Regulatory strategy experience
EU and US FDA strategy and engagement
Experience In Oncology Is Highly Preferred
Experience in Phase 3 trials
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.