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I have spent 3.9 years in the Pharmacovigilance industry. I have experienced in ICSR case processing, PSSR, Literature Safety, Triage, and Aggregate Reporting. I want to join the organization that provides pharmacovigilance services to customers, and I really liked it. So, I can learn more from the company, that will increase my knowledge, career growth and fulfill organizational goals.

SEEKING A CHALLENGING CAREER WITH A PROGRESSIVE ORGANIZATION THAT PROVIDES AN OPPORTUNITY TO CAPITALIZE MY SKILLS AND ABILITIES IN THE FIELD OF PHARMACY.

Pharmacovigilance professional with experience focused on ICSR processing and regulatory submissions. Skilled in adverse event triage, MedDRA coding, and narrative generation. Known for high attention to detail and ensuring compliance with international pharmacovigilance standards to promote drug safety.

Experienced in completing clinical reviews, counseling patients and supporting physicians with information about appropriate dosages and protocols. Well-versed in medication contraindications, interactions and side effects.

Results-oriented Life Science and Healthcare Technology Professional with 1+ year of experience in clinical research, clinical data management, and pharmacovigilance. Proven knowledge of ICH-GCP, GVP, and international regulatory standards (FDA, EMA). Skilled in case processing, safety data analysis, and clinical documentation. Adept in EHR systems, CRF design, and signal detection. Demonstrated ability to collaborate with cross-functional teams and deliver high-quality, compliant documentation to support drug safety and clinical operations.

Ramana Sathiyamoorthi

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Clinical Pharmacist

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Bachelor of Pharmacy , India - Pharmacy

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Clinical Pharmacist

Intern

Bachelor of Pharmacy , India - Pharmacy

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