select * from applications_reporting where candidate_id = '' 2

Regulatory Affairs Manager (Clinical)

Negotiable | East Midlands, West Midlands |  CRO |  Permanent  | Ref:885580

Consultant

image

Katie Goulbourn

Which team do you work in?
I work within the Drug Development team.

Which area do you specialise in?
I specialise in recruiting Junior to Director level Regulatory Affairs & Quality Assurance professionals within Pharma, Healthcare, Medical Devices and Animal Health. 

How do you keep up-to-date with the issues in your sector?
Speaking daily with clients and candidates keeps me on top of the latest industry trends and news, combined with regularly visiting relevant websites and reading articles.

What's your favourite film and why?
I absolutely love a good rom-com, my favourite would have to be The Holiday.

If you could invent one thing what would it be?
Trackable GPS microchips for cats and dogs - how has this not been invented yet!?

More

The Role

Regulatory Affairs Manager, £40k-£45k, Midlands

An extremely rewarding yet demanding, fast paced role, requiring an experienced Regulatory professional to lead one of the companies project teams.

 

The Company

  • A well-established, growing pharmaceutical manufacturing and clinical trial company based in the Midlands

  • Working with a variety of pharmaceutical clients, this role will be client facing

  • Specialising in GMP and GCP manufacturing and phase 1 trials

  • Excellent company culture and team environment

  • Competitive benefits package including 33 days annual leave, pension scheme, healthcare, flexible working and onsite subsidised canteen

 

The Role

Looking for a dynamic individual to take the lead of their project team, your responsibilities would include:

  • End to end management of your delegated projects and clients

  • Preparation and submission of regulatory applications including CTAs and ARSACs

  • Acting as the regulatory point of contact throughout the company and with authorities

  • Legal obligations with regards to your clients and the MHRA

  • Dealing with all post-submission activities

 

You

To be considered for this role, candidates must be able to demonstrate:

  • A minimum of three years recent experience within a regulatory affairs role with CMC exposure

  • Excellent communication skills, confident in a client facing setting

  • Experience of preparing and submitting CTAs

  • Drug development experience highly advantageous

  • Project management experience

 

What should you do next?

This Regulatory Affairs Manager job is a great role and won't be around for long! So don't delay. If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



More jobs like thisSee all