My client has had a very successful 2011 and with this in mind they are expanding their team and office throughout 2012. With several offices throughout Europe and a focus on the UK growth now is the time to join this consultancy. You will Report directly in to the Managing Director.
JOB SUMMARY
- Provides a full range of consulting services to clients to a high quality and on time delivery.
- Is a source of regulatory expertise in the development, registration and post-licensing activities of pharmaceutical products.
- Contributes to the effective functioning of the company.
KEY DUTIES AND RESPONSIBILITIES:
- Client Activities
- Provides a full range of consulting services (strategy and writing) within personal area of expertise.
- Deliver projects on time and to a high quality.
- Project manages activities with minimal supervision.
- May act as company team-lead.
- Reviews work of junior personnel.
- Interacts professionally at multiple levels within a client organisation.
- Prepares and/or delivers presentations with the support of Management.
- Knowledge Management
- Acts to develop and maintain regulatory skills and knowledge necessary to ensure effective support to clients.
- Business Development
- Continues to build a network of industry colleagues.
- Assists Management in the preparation of proposals (e.g. researching new potential projects, determining activities required).
- Company Activities
- Develops and maintains personal contacts with regulatory agencies or professional associations to build confidence in and enhance the reputation of the company.
- Develops junior personnel through mentoring.
- Completes basic job related responsibilities e.g. maintenance of personal training record, timesheets, project archiving.
MINIMUM REQUIREMENTS
- Education and Experience
- Life sciences or chemistry graduate.
- Sound knowledge of European pharmaceutical regulations and guidelines. Conversant with the primary functions of product development, microbiology, toxicology, clinical research, manufacturing and quality assurance.
- Significant regulatory affairs experience including a successful track record in the registration of medicinal products within Europe.
- Essential Skills and Abilities
- Excellent written and verbal communication skills.
- Established relationships and proven negotiation skills with management, colleagues and regulators.
- Computer literate.
- Good organisational skills.
- Good analytical skills.
Even if you are unsure on your suitability for this position but you are looking at the possibility of some progression in your current job or a change in your career path, please feel free to contact me for a friendly chat to explore any options that may be open to you.All enquiries will be dealt with in a strictly confidential manner.
Call Matt on 01293 776644 or email me at mhart@barringtonjames.com
The personal touch that brings results