Clinical executive

Job Title:Clinical ExecutiveDepartment:Meril Academy Global – Clinical AffairsLocation:IndiaReports To:Manager / Senior Manager – Clinical Affairs / Meril Academy GlobalJob Purpose:To support and execute clinical studies, trials, and observational research activities while developing high-quality clinical documentation, scientific outputs, and regulatory-ready evidence. The role contributes to patient safety, product credibility, and scientific excellence through close collaboration with internal teams and external clinical experts.Key Responsibilities:1. Clinical Studies & Research Management• Oversee and support clinical studies, clinical trials, and observational research in line with approved protocols and ethical standards.• Coordinate with investigators, sites, CROs, and internal teams to ensure timely and compliant study execution.• Monitor study progress, data quality, and adherence to clinical and regulatory requirements.2. Clinical Documentation & Protocol Development• Develop, review, and finalize study protocols, investigator brochures, CRFs, and SOPs.• Ensure clinical documentation meets internal quality standards and applicable regulatory guidelines.• Maintain accurate and up-to-date clinical study records.3. Clinical Reporting & Scientific Writing• Prepare clinical summaries, study reports, and scientific documents for regulatory submissions, internal reviews, and publications.• Support data interpretation, clinical evidence generation, and scientific communication.• Contribute to abstracts, manuscripts, posters, and presentations as required.4. Publication Planning & KOL Collaboration• Collaborate with cross-functional teams and Key Opinion Leaders (KOLs) on publication planning and scientific dissemination strategies.• Support timely execution of publication activities in alignment with clinical and regulatory milestones.• Ensure ethical, transparent, and compliant scientific communication.5. Clinical Expertise & Advisory Support• Serve as a clinical subject matter expert for internal teams including Sales, Marketing, R&D, Quality, and Medical Education.• Address clinical queries from external stakeholders with evidence-based insights.• Advise on product use, patient safety, risk mitigation, and best clinical practices.Qualifications and Experience:• Bachelor’s / Master’s degree in Biomedical Engineering, Medical Research, Life Sciences, or a related healthcare / technical field.• Minimum 2 years of experience in clinical studies, trials, or observational research.• Experience working with medical devices or regulated healthcare environments is preferred.Skills and Competencies:• Hands-on experience in overseeing clinical studies, trials, and observational research activities.• Strong capability in developing study protocols, CRFs, SOPs, and clinical/regulatory documentation.• Proven expertise in clinical data interpretation, scientific writing, and publication planning.• Ability to collaborate effectively with KOLs, investigators, and cross-functional teams.• Strong analytical, documentation, and problem-solving skills.• High standards of accuracy, ethics, and attention to detail.• Clear and professional communication skills in English (written and verbal).Key Performance Indicators (KPIs):• Timely and compliant execution of clinical studies and research activities• Quality and accuracy of clinical documentation and reports• Effectiveness of clinical data interpretation and scientific outputs• Contribution to publications and evidence generation• Responsiveness and quality of clinical advisory support• Adherence to patient safety, ethical, and regulatory standardsRefer or apply to

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