Clinical Executive

Roles & Responsibilities
• Support and oversee clinical studies, clinical trials, and observational research activities
• Coordinate with investigators, clinical sites, CROs, and internal cross-functional teams
• Develop, review, and maintain study protocols, CRFs, Investigator Brochures, and SOPs
• Prepare clinical study reports, summaries, and regulatory submission documents
• Contribute to scientific writing including abstracts, manuscripts, posters, and presentations
• Collaborate with Key Opinion Leaders (KOLs) for publication planning and scientific dissemination
• Provide clinical advisory support to Sales, Marketing, R&D, and Quality teams
• Ensure compliance with ethical guidelines, regulatory requirements, and patient safety standards

Qualification
• Bachelor’s or Master’s degree in Biomedical Engineering, Medical Research, Life Sciences, or related discipline

Experience
• Minimum 2 years of experience in clinical studies or clinical trials
• Prior experience in medical devices or regulated healthcare environment preferred

Skills
• Clinical protocol and CRF development
• Scientific and medical writing
• Clinical data analysis and interpretation
• Regulatory documentation and compliance
• Effective communication with investigators and KOLs
• Strong attention to detail and ethical research practices

About the Organization
Meril is a globally recognized medical device company committed to innovation, clinical excellence, and patient safety. Through Meril Academy Global – Clinical Affairs, the organization focuses on high-quality evidence generation, scientific advancement, and regulatory-compliant research, offering professionals strong career growth and global exposure.