Academic & Regulatory Affairs Manager

Key Responsibilities:

• Support research and development activities by conducting thorough academic literature searches.
• Develop and deliver compelling presentations (PPTs) on contemporary health and pharmaceutical topics.
• Create and maintain regulatory documents in compliance with industry standards.
• Stay updated with and apply knowledge of Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Good Laboratory Practice (GLP) regulations.
• Clinical trials and pharmaceutical regulations and guidelines.
• Collaborate with cross-functional teams to support regulatory submissions and compliance initiatives.

Qualifications:

• PhD/post-graduate degree in Pharmacy or a related field.
• Training in GCP, GMP, GLP, and other relevant regulations.
• Proficiency in Microsoft PowerPoint and other presentation tools.
• Strong understanding of pharmaceutical regulations and compliance requirements.
• Strong understanding of regulatory requirements and provisions for medical devices.
• Excellent research and analytical skills for academic literature searches.
• Exceptional attention to detail and organizational skills.
• Ability to work independently as well as part of a team.
• Experience of 2-3 years in the relevant field is preferred.