Regulatory Affairs Consultant
- South East
- Contract
- Drug Safety / Pharmacovigilance
Our global Pharmaceutical client based in leafy Hertfordshire is now looking for an experienced Regulatory Consultant to join their developing team on a contractual basis within their Vaccines therapeutic field.
We are looking to on-board and enthusiastic professional for a period of 5 months and duties will include the following.
- Planning and executing updates to the HRM system in support of business operations relating to the United Kingdom leaving the European Union
- Ensuring the entry of accurate, complete and timely Regulatory Information into the HRM system
- Provide detailed updates at key milestones to ensure all activities are completed on time and within the project plan
- Bachelor’s degree with 2 years of industry experience in a regulatory/compliance industry with an emphasis on system support
- General global regulatory knowledge
- Knowledge of EU regulatory procedures e.g. MRP/DCP, CP
- Ability to follow instructions and work independently abroad organizational awareness and knowledge of touchpoints/interdependencies
- Demonstrated problem-solving skills
- Proven experience analyzing information in support of data entry activities
- Excel, Word and PowerPoint
If this position is of interest, please do not hesitate to get in touch.
The candidate must have the rights to work in the location stated in the job advert.
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