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Regulatory Affairs Manager CTA

Central London   •  Negotiable  •  Permanent, Full time


Regulatory Affairs Manager Clinical Trials

Location Remote (Europe)

Regulatory Affairs Manager Clinical Trials position working for a global clinical research organisation.

The role will be responsible for overseeing clinical trials globally and as a regulatory affairs manager, you will be responsible for preparing and maintaining core clinical trial dossiers in unity with regulatory requirements.

Responsibilities

-Ability to write scientific documents e.g. Investigational Medicinal Product Dossier, Investigators Brochure, clinical trial justifications with minimum support of senior staff.

-Involved in strategically planning and overseeing global country submissions.

-Interacts with internal and external clients to provide regulatory guidance and strategic input for clinical trials.

-Train and mentor junior members and give clinical trial advice.

Requirements

-A degree in life sciences or a relevant qualification.

-5 to 6 years in regulatory affairs specifically focused on clinical trials.

-Previous experience working with global clinical trial submissions.

The role also comes with an excellent benefits package and the flexibility of working fully remotely across multiple locations in Europe.

If you are interested in this role or would like more details please email your CV to lucy.kirkaldy@cpl.com

  • Agency: Cpl Life Sciences
  • Reference: JO-2207-497777
  • Posted: 21st September 2022
  • Expires: 19th October 2022

Cpl Life Sciences

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