A typical projects could involve co-ordination of worldwide renewals and safety reports in one or two core therapeutic area. Acting as initial Point of contact for the client and managing the internal team to ensure timely and quality deliverables.
Candidates should have a strong academic background in a life science discipline, extensive experience in regulatory affairs specifically in post approval maintenance activities in both the EU and ROW including variations, licence renewals, annual reports and periodic safety update reports. You will have strong written and oral communication skills, commitment to highest quality outputs, high attention to detail, a professional service mentality, and an ability to build rapport and strong relationships with both internal and external colleagues. As your team will be based in India you will have experience of remote people management.
Kinapse is a fast-growing, values driven company with a supportive team and can offer you a rewarding and challenging career working with smart, ambitious, yet humble professionals. We offer both office and home-based roles, and a competitive salary with a range of benefits.
If you want to be part of a progressive, forward-thinking company and want to make a difference we would really like to hear from you!
Please forward a copy of your CV and covering letter confirming your salary expectations.