Regulatory Consultant - CTA (remote)

Proclinical are partnering with a CRO who are recruiting for an individual to join their team on a contract and remote basis. The opening position that is currently available at this client's organisation is for a Reg Consultant.

Responsibilities:

• Enable transversal cooperation between divisions for the delivery of all proposals of multifaceted large clinical trials in a timely manner.
• Offer guidance and knowledge in both regulatory and proposals linked aspects of clinical trials.
• Serve as the main point of contact for the client as well as distribute proposal-specific milestones.
• Contribute to EU-CTR consulting as well as to 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 as well as project management.
• Expertise on proposals under EU-CTR directive.
• Know-how of clinical trial submissions on both a local and regional level.
• Able to resolve issues.
• Customer focused with the ability to work well both independently as well as in a team.
• 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 Peter Duvall at p.duvall@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.

#Regulatory