Regulatory Affairs Specialist

1 week ago

Cambridge, United Kingdom Alimentiv Full time

**POSITION LOCATION**: Canada, US, Germany, Netherlands, UK

**POSITION TITLE**: Regulatory Affairs Specialist (Full-time, Permanent)

**POSITION REPORTS TO**: Manager, Regulatory Affairs

**DEPARTMENT/UNIT NAME**: Regulatory Affairs - Clinical Research

**JOB SUMMARY**:
**ROLE AND RESPONSIBILITIES**:
**Unit Management**
- Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
- Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.

**Client Services**- Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.

**Regulatory Strategy Development**
- Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
- Participate in specialized conferences/meetings to increase knowledge as needed.\

**Project Support**
- Regularly respond to registration requests and work with project teams to identify regulatory requirements.
- Assist in the preparation of regulatory submissions and support summaries.
- Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.

**QUALIFICATIONS**:
**WORKING CONDITIONS**:
Office/Home-based
- Accommodations for job applicants with disabilities are available upon request.

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