Typical projects will involve analysis and reporting of clinical data and information, working on a range of regulatory documents including but not limited to, protocols and amendments, CSRs, IBs, INDs, clinical summaries and overviews, briefing documents, response to authorities, and PIPs. As well as authoring more complex document types, we provide opportunities to review and perform quality checks on documents prepared by junior writers, so you will have the chance to pass on your expert skills and knowledge to coach, mentor and train team members.
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.
Candidates should have a strong academic background in a life science discipline, extensive experience in regulatory writing either as a part of pharmaceutical or CRO Company, 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.
What we can offer you.
Kinapse can offer you a rewarding and challenging career working with smart, ambitious, yet humble professionals. We pride ourselves on having a non-hierarchical and friendly office culture where people are prepared to go the extra mile to help one another. If you’re lucky enough to work in our Wimbledon office we have some great social events every month. 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!