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Regulatory Affairs professional with 7+ years of progressive experience supporting Class I, Class II, and Class III medical devices representing Cardi... View More
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Experienced in clinical research coordination and managing multi-disciplinary clinical trials from initiation to closeout, ensuring regulatory complia... View More
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Certifications
- Society of Clinical Research Associates (SOCRA), Certified Clinical Research Professional (CCRP) 2024
Results-driven Analytical Chemist / Laboratory Technician with strong hands-on experience in method development, validation, and stability testing of ... View More
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Experienced Clinical Research Leader 14+ Years in Clinical Operations Experienced Clinical Research professional with 14+ years in late-phase t... View More
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Certifications
- SAS Programming -High Technology Solutions, Sky Infotech, Noida.
- PG Diploma in Clinical Research, Pharmacovigilance, and Data Management -Jaipur National University, Delhi
- Diploma in Drug Regulatory Affairs - Bioinformatics Institute of India, Noida
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse... View More
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Certifications
- ICH-GCP and IATA Certified
Scientist with excellent productive research experience in multi-disciplinary areas of life sciences. Strong technical & problem-solving skills in vir... View More
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Dynamic recent graduate with an MSc in Formulation Science, with a focus on pharmaceutical and cosmetic sciences. Eager to start a fulfilling career ... View More
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Certifications
- The International Society for Pharmacoeconomics and Outcomes Research (ISPOR) (08/2019 - 07/2022) ABMH PharmaCon- VII (2019) Social Transformation through dynamic education (2020) IPASF (Indian Pharmaceutical Association Students Form) (01/2017 - 01/2018)
7 Years’ experience in clinical research spread across 6 therapeutic areas (Oncology, Neurology, Cardiovascular diseases, Hematology, Endocrinology an... View More
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Certifications
- Regulatory Compliance and Informed Consent Process: Veeva Vault QMS: DocuSign, Adobe Sign, Veeva Vault eTMF. Clinical Data Management: Medidata Rave, Oracle Clinical, SAS Clinical Data Integration. Clinical Study Reports (CSRs
Dedicated & detail-oriented Sr. Clinical Trial Assistant with 7+ years of experience in facilitating clinical trials by providing administrative supp... View More
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Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeab... View More