|Job title :||Associate Director; Regulatory Submissions Writing|
|Job type :||Permanent|
|Salary :||Up to £140000 per annum + Exceptional remuneration & benefits|
|Contact name :||Harriet Lawford|
|Contact email :||email@example.com|
*You will be responsible for writing and overseeing the writing of complex regulatory documents for submission to regulatory authorities in support of drug development and marketing applications.
*You will contribute scientifically and strategically at the project and/or study team level to facilitate efficient development of high-quality clinical documents for regulatory filing as well as be further responsible for training and mentoring more junior individuals within the team.
*This is a leadership position with strong prospects for line management (currently hiring additional scientists to support you)
What's in it for you?
I have not come by a company with such great benefits in a long time! Stock options, car allowances, travel allowances, 28 days annual leave, 9 bank holidays AND an additional Christmas shut down not to mention an incredibly lucrative budget. You can also enjoy 2 days a week from home as well as all the standard benefits for you and your dependants!
In addition to this the role has huge scope for growth inclusive of building a team! So you will be constantly challenged within the role, not one of those stagnant positions we see in large global pharma all too often!
To be considered for this role you will need to have at 5 years' experience in all aspects of regulatory writing, ideally during all phases of drug development and commercialization (investigational, registration, pre- and post-launch, marketed). This can be from Pharma or Biotech.
Knowledge is power
To find out more about this excellent opportunity apply today. If you would like a confidential conversation on how this role will fit with your own needs or experience, then please do get in touch.