Regulatory Affairs Consultant
Major Pharma based Bedfordshire.
Initial contract period - 6 months.
Introduction
My client is a major pharmaceutical company, and has a portfolio of products for major disease areas including cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation. Employing over 11,000 people in the UK alone, my client has an international presence, with offices also in United States, Sweden, France, Canada, India, China and Japan.
Job Summary
My client, a leading pharmaceutical company, is seeking a Regulatory Consultant to join the team on an initial 6 month contract with potential for extension beyond. This is a role which offers a super opportunity to be hands on in competitive licence, strategy development and implementation, compliance and commercial support.
This role will be based within a small team, specialising in the UK, Irish and Maltese markets and will report to the Regulatory Affairs Manager. Although this role is fully office based, there may be some opportunity to travel both internationally and domestically on occasion.
Essential Skills & Qualification
- Bachelors degree in a life science or related subject
- Experienced in working^in a Matrix environment and with teams of varying size
- Significant experience of working within a regulatory team is essential
- Full lifecycle experience would be advantageous
Supplementary Requirements:
Software Competence: MS Office, DOCUMENTUM
Valid Driving License: Essential
Working Language(s): English
Requirement for Business Travel: Yes - limited
Flexible Working Hours: No
Employment Information:
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 6 Months
Location: UK; Office Based in Bedfordshire
Plan Start Date: July / August 2012, Please do not apply if you are unable to meet this start date.
Contract Benefits: Day Rate inclusive of benefits
Keywords:
MS Office, DOCUMENTUM, Registration, Regulatory Affairs, MAA, CMC, Expert Reports, Clinical Trial Applications, CTA, CPMP, Dossier, Regulatory Agency
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.