Senior Regulatory Affairs Manager
Large Bio-tech based in Cambridge
Contract role - 12 Months
Introduction
Our client is a leading Fortune 500, Biotechnology Company. With headquarters in the USA, my client employs over 500 staff in their UK^offices, located in Cambridge and Middlesex on both a permanent and contract basis.
A market leader, my client strives to develop products that change people's lives and in the last 30 years have transformed the management of anaemia, inflammation, and cancer. They have a thriving pipeline and are currently very active in recruiting candidates to join the team on a contract basis.
Both UK sites are easily reachable by mainline BR and have excellent road links with ample free car parking.^
Our client knows they offer a great place to work. Our client understands that each candidate is not the same, and no two roles are either. That's why they permit up to two days working from home per week depending on the role. Moreover, it's a^place where you will be more than a contractor-you will be one of the team, and that even means an early Friday finish!
Job Summary
Located in the Cambridge office, my client is seeking a Senior Regulatory Manager to join the team. This role^is varied. The successful candidate will be working on a portfolio of both development and marketed products in Oncology, so complete lifecycle experience from CTA applications through to MAA applications and post marketing activities is essential.^This is a NEW VACANCY and our client is keen to interview and move to offer ASAP, so it is essential to move quickly, should you be interested in this post.
Although working predominantly in EU markets, you should also have some experience in working across international markets, including the US and particularly in the review and approval of promotional and non promotional materials, although ability to sign off is not essential.
Essential Skills & Qualification
- BSc (or higher) in related subject
- Proficient in submitting CTAs & PIPs
- Excellent project management skills are
- In depth understanding of the VHP.
- Ability to communicate effectively and clearly across all levels
- Time management skills and the ability to prioritise workload.
Supplementary Requirements:
Software Competence: MS Office, MS Project, DOCUMENTUM
Valid Driving License: Not Required
Working Language(s): English
Requirement for Business Travel: Limited travel may be required
Flexible Working Hours: To be confirmed
Employment Information:
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 12 Months
Location: Office Based in Cambridge
Plan Start Date: ASAP
Contract^Benefits: Day Rate inclusive of benefits
Keywords:
MS Office, MS Project, DOCUMENTUM, Registration, Regulatory Affairs, MAA,CMC,Expert Reports, Clinical Trial Applications, CTA, CPMP, Dossier, Regulatory Agency, Documentum
Assigned Consultant: Kirsty Clark at CSL Recruitment on 01932 234 681
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs, applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We request that non EU Nationals include evidence of right to work in the country concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day rate if you are a new candidate.