Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s who you could be too.
Working fully embedded within one of our pharmaceutical clients, with the support of PRA right behind you, you’ll be at the heart of our client’s innovation.
As a Manager of Global Regulatory Affairs, you will be dedicated to one of our pharmaceutical clients with a truly global presence; this unique industry-changing partnership redefines collaboration. The program is ideal for individuals who thrive in a continually-evolving culture that mirrors PRA’s commitment to career development.
The Manager of Emerging Markets Regulatory Affairs (EMRA) is aligned to the client’s portfolio of licensed products. The manager is responsible for the RA activities of assigned products in Emerging Markets working in collaboration with the client’s global functions and affiliate companies and partners across EM.
Providing EM strategic and functional input to the global team, the Manager of EM Regulatory Affairs will plan, manage and execute regulatory activities on licensed products.
Other responsibilities will include:
A team worker with the ability to influence in order to achieve objectives. You will have excellent organisational skills, flexibility and attention to detail along with a mind-set towards adherence to timelines.
Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have: