Paridhi Anand

About Paridhi Anand

Experience with Drug Safety/Pharmacovigilance in the pharmaceutical industry• Expertise in data entry/data analysis experience with Argus • Knowledge of processing both clinical trial drugs as well as post marketing drugs• Proficient knowledge of MedDRA and WHO-DD coding dictionaries and grouping terms• Execute case submission via MedWatch/CIOMS I and E2B forms • Knowledge of submission of IND Annual reports• Experienced with identifying and handling inconsistent and incomplete source documents and patient reports• Proficient in ICH/GCP regulations, FDA guidelines as well as EMEA guidelines• Excellent understanding of the clinical trial phases and the post- marketing process• Excellent with MS Word, Powerpoint, Excel, Adobe Acrobat• Exceptional interpersonal and communication skills• Good, clear, effective writer and speaker• Excellent analytical and logical thinking skills• Team player, great attention to detail, eager to learn new skills and take on responsibilities• Ability to work effectively and efficiently in a high pressure, fast paced environment

Experience

1. Director of Pv Operations

   Moderna

   Jan 2023 — Present

Education

• University of the Sciences in Philadelphia - Philadelphia College of Pharmacy

  Bachelors, Pharmacology and Toxicology

Skills

• Word
• Infectious Diseases
• Clinical Research
• Cioms
• Ich-Gcp
• Package Inserts
• Ind/Maa
• CRO
• Standard Operating Procedure (Sop)
• Meddra
• Emea
• Sas
• U.s. Food and Drug Administration (Fda)
• Psurs
• Regulatory Affairs
• Clinical Development
• Microsoft Excel
• Powerpoint
• Medwatch
• Oncology
• Biotechnology
• Argus
• Excel
• Gcp
• Pharmaceutical Industry
• Sop
• Fda
• Drug Safety
• Regulations
• E2b
• 21 Cfr
• Postmarketing
• Who-Dd
• Good Clinical Practice (Gcp)
• Pharmacovigilance
• Clinical Trials