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Detail-oriented and accomplished 'Medical Writer' with over 4 years of specialised experience in clinical safety documentation and pharmacovigilance. Demonstrated success in preparing regulatory documents including CSRs, PBRERs, PADERs, DSURs, and signal assessments. Skilled in MedDRA coding, data validation, and compliance with international regulatory standards including ICH, FDA, and GVP. Adept at collaborating with cross-functional global teams and mentoring new recruits.

Medical Writer, Medical Reviewer, and Scientific Communications Professional with 5+ years of experience spanning medical writing, scientific publications, healthcare communications, medical review, and pharmacy education. Experienced in developing manuscripts, systematic reviews, meta-analyses, clinical and regulatory documents, medico-marketing content, oncology materials, and patient education resources. Trained in Regulatory Medical Writing through a Post Graduate Diploma in Medical & Regulatory Writing from Henry Harvin Institute. Strong understanding of clinical research, scientific communication, publication development, literature review, evidence synthesis, and regulatory guidelines including ICH-GCP, FDA, EMA, and CDSCO.

Strategic Project Leader with 10+ years of cross-functional pharmaceutical expertise spanning Quality Assurance, Process Compliance, Clinical Research, and Pharmacovigilance. Proven architect of operational frameworks, process models, and Quality Management System (QMS) workflows designed to ensure alignment with cGMP and global regulatory requirements. Expert in managing complex external stakeholder relationships, driving continuous improvement, and enforcing rigorous data integrity standardizations across cross-functional matrix teams.
Professional medical writing expert with robust experience in creating accurate, clear, and concise medical content. Proven track record in translating complex medical research into accessible materials for diverse audiences. Strong focus on team collaboration and achieving results, adaptable to changing needs. Skilled in scientific writing, literature review, and regulatory documentation, with high level of attention to detail and reliability.

Detail-oriented team player with strong organizational skills. Ability to handle multiple projects simultaneously with a high degree of accuracy.

Nilam Kad

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Associate Medical Writer

Lab Technician

Lab Technician

Intern

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ADMLT -

PGDM in Clinical Research -

Master of Science - Microbiology

Bachelor of Science - Microbiology

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Associate Medical Writer

Lab Technician

Lab Technician

Intern

PGDM in Clinical Research -

ADMLT -

Master of Science - Microbiology

Bachelor of Science - Microbiology

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