Regulatory Affairs Assistant

Join our international team and support regulatory aspects of clinical research projects. Youll help streamline communication manage documents and maintain key systems - all while learning from experienced regulatory professionals.

Office-Based in Bangalore India

What Youll Do:

• Communicate with project teams on regulatory matters and serve as a support contact for PSI services
• Maintain departmental tracking systems and regulatory calendars
• Support the preparation of regulatory submissions and license applications under supervision
• Perform quality control on outbound documents and manage filing with Document Management Systems
• Translate regulatory documents as needed
• Provide technical assistance with regulatory feasibility research
• Train PSI staff on departmental software and provide administrative support to the Regulatory Affairs team

Qualifications :

• College/University degree or an equivalent combination of education training & experience
• Life Science degree is a plus
• Prior experience in Clinical Research
• Common European Framework of Reference for Language (CEFR) B2 level in English.
• Proficiency in MS Office applications
• Ability to plan multitask and work in a dynamic team environment
• Communication and collaboration skills

Additional Information :

What we offer:

• We value your time so the recruitment process is as quick as 2-3 meetings
• Well prepare you to do your job at highest quality level with our extensive onboarding program
• Youll have permanent work agreement at a stable privately owned company
• Were constantly growing which means opportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Remote Work :

No

Employment Type :

Full-time