Regulatory Affairs Professional

Proclinical are partnering with a CRO who are recruiting for an individual to join their team. The opening position that is currently available in this company is for a qualified Regulatory Professional. This role is on a contract basis with the ability to work from various parts of Europe on a remote basis.

Responsibilities:

• For this role, you will be responsible for offering guidance and knowledge in regulatory and proposals linked aspects of clinical trials.
• The ideal candidate will be accountable for serving as the main point of contact for the client and deliver on proposal-specific milestones.
• Accountable for providing leadership on proposals knowledge to clients.
• As the Regulatory Affairs Specialist, you will enable transversal cooperation between divisions for the delivery of all proposals of multifaceted large clinical trials in a timely manner.
• You will be responsible for contributing to EU-CTR consulting and partake in its operational execution.
• Other duties may be assigned.

Key Skills and Requirements:

• Educated to a degree level in a scientific field.
• A background in clinical trial management.
• Familiarity within regulatory affairs.
• Expertise on clinical trial proposals on both a local and regional level.
• Know-how of proposals under the EU-CTR directive.
• Acquaintance in project management.
• Able to resolve issues.
• Customer focused with the ability to work both in a team as well as independently.
• Fluency in the English language with knowledge in the local language.
• Communication skills both verbally and in writing.

If you are having difficulty in applying or if you have any questions, please contact Dracen Black at d.black@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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