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Job Details

Regulatory submission coordinator – The Netherlands **Brand new**

Company: Barrington James Europe
Location:
Reference: subregnethLH
Closing Date: 29 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

After an exciting partnership with a leading, top 10 CRO, I am looking for experienced professionals to join the company in a Regulatory submissions coordinator position. For more information on what this challenging and rewarding opportunity can offer you, apply now!

Requirements:

After an exciting partnership with a leading, top 10 CRO, I am looking for experienced professionals to join the company in a Regulatory submissions coordinator position.

 

The company work across all stages of development, and are extremely particular about the trials they decide to undertake, meaning you will have the opportunity to work on only the most exciting clinical trials and within an environment that is never stressful or unmanageable.

 

As a Regulatory submissions coordinator you will be responsible for the preparation, review, and filing of all Regulatory submissions, including clinical trial applications to domestic and internal regulatory agencies. As well as ensuring all submissions comply with the applicable regulations and guidance documents.

 

You will have the opportunity to advise sponsors on changing regulations and compliance requirements, plus track submissions and ensure timely filling of documents.

 

Experience required:

 

Bachelor’s degree in life sciences
Hands on experience of preparing, reviewing and submitting regulatory documentation
Minimum of one year’s experience as a regulatory submissions coordinator

 

For more information on what this challenging and rewarding opportunity can offer you, apply now!

Apply for this job: Regulatory submission coordinator – The Netherlands **Brand new**

Contact Information:

Address:  Head Office
Rowan House Smallfield Road Horley Surrey
RH6 9AU
England
Tel:  01293 776644
Fax:  01293 822333

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