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Are you an experienced pharmaceutical professional looking to work in a dynamic, cutting edge and fast-growing biotech environment?
Our client has an exceptional Regulatory Specialist position working for this pioneering immunotherapy focused clinical-stage biotech company based in the Netherlands.
The company has pioneered, developed and optimised their in-house cell production processes, having recently received orphan drug designation for their lead investigational product.
As part of their rapid expansion they are now looking to recruit an experienced professional to lead the maintenance, drafting and reviewing of company submissions in support of their ATMP clinical trials (IND/IMPD).
The right person for this role will have 3-5 years of demonstrated regulatory affairs experience (clinical IND/IMPD) or a detailed Clinical & Scientific Project Management background, a familiarity with EU & US clinical legislation procedures, strong project management skills and a willingness to be positively flexible in their role.
This is a unique opportunity to work for an internationally recognised biotech which has very exciting growth plans.
The role is not a standard regulatory position and offers the right person a genuine chance to accelerate their career and be part of a truly unique development process.
Expired
- Location: North Brabant
- Salary: Highly competitive salary & benefits
- Job Type:Permanent
Posted over 4 years ago
- Contact: Jake Thomas
- Contact Email: jake.thomas@nextphaserecruitment.com
- Contact Phone: 01403 216216
- Start Date: 2020-12-01
- Job Ref: V-46429-1
Our client has an exceptional Regulatory Specialist position working for this pioneering immunotherapy focused clinical-stage biotech company based in the Netherlands.
The company has pioneered, developed and optimised their in-house cell production processes, having recently received orphan drug designation for their lead investigational product.
As part of their rapid expansion they are now looking to recruit an experienced professional to lead the maintenance, drafting and reviewing of company submissions in support of their ATMP clinical trials (IND/IMPD).
The right person for this role will have 3-5 years of demonstrated regulatory affairs experience (clinical IND/IMPD) or a detailed Clinical & Scientific Project Management background, a familiarity with EU & US clinical legislation procedures, strong project management skills and a willingness to be positively flexible in their role.
This is a unique opportunity to work for an internationally recognised biotech which has very exciting growth plans.
The role is not a standard regulatory position and offers the right person a genuine chance to accelerate their career and be part of a truly unique development process.