European Regulatory Affairs
vor 3 Wochen
Proclinical are recruiting a European Regulatory Affairs - CTA Liaison for a biotech corporation. This role is on a contract basis and is located in Zug.
**Responsibilities**:
- Collaborate with regulatory affairs consultants/service suppliers on CTA proposals.
- Serve as a representative for EU regulatory affairs at cross-functional study management team meeting.
- Discuss and educate cross-functional teams on European regulatory needs and alterations within the regulatory landscape.
- Partake in the regulatory method by bringing the European acumens into conversations.
- Uphold expertise on regulatory needs and regulations.
- Other duties may be assigned to this role.
**Key Skills and Requirements**:
- Educated to a degree level in a life science field.
- Fluency in the English language.
- Know-how of the European drug development process and regulatory needs.
- Communication skills both verbally and in writing.
- Technical/analytical abilities to resolve issues.
- Able to handle various projects simultaneously.
- Capable of balancing regulatory goals with business goals.
- Works well with others.
- A motivated individual.
- An organised individual with the ability to prioritise own workload.
- Works well while under pressure and able to meet deadlines.
- Seeks out and suggests process improvements.
- Eager in joining a fast-paced, small-company setting.
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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