Regulatory Officer (submissions)

Regulatory Officer – Clinical Trials

Germany – Munich (Full Time), on-site

Salary - €55-65k plus benefits

Working for an established provider of clinical trials with a reputation globally for providing excellent services within clinical research, we are looking for a Regulatory Officer to join our clients international team.

This exciting opportunity will involve working together with our client’s team of regulatory and ethics submissions specialists where you will play an integral role in the start up of research projects covering a wide range of therapeutic areas. Ideally you will have already gained a minimum of 12 months clinical trial submissions experience and be looking for a company to help support you in your career development. Our client has an excellent reputation for supporting its employee’s wellbeing and career progression.

Typical responsibilities will include

• Clinical trial submissions for regulatory and ethics authorities

• Working closely with project teams, vendors and regulatory authorities

• Safety reporting

• Helping and support feasibility research and business development requests

• Regulatory training to project teams as and when required.

• Tracking of regulatory projects

Qualifications and experience required

• Degree in the life sciences or equivalent

• Austrian clinical trial submissions experience

• Fluency in written and spoken English and German

• Detail orientated with excellent communication and MS Office skills

Previous clinical trial submissions experience as well as fluency in English and German (B1 and above) is essential for this opportunity. If you have the skills required and the right to work in Germany and would like to discuss the full details of the job, please contact Louise Clark on +44 (0)1293 364114, or apply with your CV.