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Sujata Bhoi, Ph.D

Clinical Trial Manager at Sciadonics

Sujata Bhoi, Ph.D. has extensive experience in the clinical drug development and research fields. From 2009 to 2019, they held various positions in research and clinical trial management. In 2009, they were a Research Assistant at Jawaharlal Nehru University, where they were responsible for DNA and RNA isolation, PCR, qPCR, Electrophoresis, Cloning, Southern Blotting, Site-directed mutagenesis, and Sequencing. In 2010, they worked as a Senior Research Fellow at the International Centre for Genetic Engineering and Biotechnology, where they were responsible for Cloning, Protein Purifications, SDS PAGE, Western Bloting, Cell culture, and Malaria. From 2011 to 2012, they were a Research Assistant in the Department of Immunology, Genetics and Pathology at Uppsala University, and from 2012 to 2018, they worked towards a Doctor of Philosophy (PhD) in Medical Science (Hemato oncology). In 2019, they began working at Medivir AB as a Clinical Trial Manager and Medical Research Associate. Her roles included managing clinical operational activities, eTMF/TMF review, QC and reconciliation, sponsor oversight of clinical trial conduct, clinical data oversight, review, proof read and QC of clinical trial documents, actively involved in Medical affairs and Scientific communication, regulatory submissions to EMA and FDA, and study initiation and study closure activities.

Sujata Bhoi, Ph.D. completed a PhD in Medical Science (Hemato oncology), 240 ECTS from Uppsala University in 2012-2017. Sujata also completed a Post graduate diploma in Computer Application from Sambalpur University in 2006-2007, and a Master's degree in Life Sciences from Sambalpur University. In 2018-2019, they completed a Clinical Drug Development (CDD), 30 ECTS program from Uppsala University. Additionally, they have obtained certifications in Medical Marketing, Pharmacovigilance training (Drug safety, Global Regulatory requirements, Audit, Signalling and Risk Assessment), Regulatory Affairs (RA) and Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), Visualize your Science, Academic Teacher Training, Basic Bioinformatics, Introduction to Scientific Research, and Scientific Writing from various institutions.

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Timeline

  • Clinical Trial Manager

    May, 2020 - present

  • Medical Research Associate

    May, 2019