Due to ongoing global expansion, Innovaderm is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and/or part II following EU CTR and other applications created within or outside of the company to ensure documentation comply with applicable regulations and guidelines and contractual timelines are met. You will provide leadership for assigned projects regarding all regulatory activities that lead to start up of clinical trials.

This role will be perfect for you if:  

• You have at least 2 years experience in regulatory affairs;
• You have experience with oversight of preparing and submitting part I and/or part II Clinical trial applications following EU CTR
• You thrive working in a collaborative environment in an expansion mode;
• You wish to share your excellent knowledge of applicable EU regional regulatory guidelines;

Responsibilities:

• Preparation of regulatory documents, CTA packages, and submissions in assigned countries to ensure high quality standards
• Coordination of regulatory timelines and deadlines for all assigned projects planned for CTIS submissions. Includes oversight of EU (mainly), APAC, and North America submissions.
• Review of regulatory documents and submissions created outside of the company by subcontractors (eg, partner CROs, regulatory vendors) to ensure high quality standards before submission to CTIS
• Point of contact for Sponsors and subcontractors/project management teams for all aspects related to study regulatory submissions
• Preparation or review of country specific Patient Information Sheet/Informed Consent form documents. 
• Preparation or review of study-specific templates of regulatory forms. 
• Manages translation requests with vendor. 
• Regulatory support and advice to project teams and key internal/external customers on local requirements and EU submission strategy and technical expertise
• Maintain high level knowledge about EU CTR and EU/EEA countries local requirements in the area of company interest.
• Maintain the regulatory intelligence database
• Participation in Kick-off meetings, audits, and other project related meetings according to the company / client needs