Senior Regulatory Affairs Associate – 12 Months Contract

RBW Consulting
10 Oct 2018
14 Oct 2018
Contract Type
Full Time
In a highly competitive Regulatory Environment, it is rare that an opportunity comes up for an Innovative, Global and truly household name within Pharmaceuticals.

This company are one of the top 10 companies in the world for their industry and they are a truly revolutionary business that is known for good employee satisfaction and development.

Currently, this business is looking to recruit a Senior RA Associate on a contract basis for 5 days a week for a full 12 month period (they are also prepared to offer extensions provided the candidate is meeting the requirements).

For this role, a candidate will need to have experience in Clinical Trial Applications (CTAs) and submissions of the same. It would also be ideal if the candidate has experience working on Eastern European submission (Including Russia) however, this is not a set requirement.

Responsibilities include (but aren’t limited to):

Act as regulatory lead for a program (under the supervision of Senior RA Lead)
Conduct pre-filing activities
Creation and submission of RA documents
Maintain CTA / MA documentation support (e.g. variations etc)
Collaborate and liaise with CRO’s and Regulatory authorities

If this role sounds like something that could be interesting to you, then Apply Now!

(This role has a limited amount of applications – this is operated on a first apply basis. If this role is of interest to you then please Apply Now for an opportunity to be considered).

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