
Dr. Bhanu Prasad
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About me
Clinical Research Associate at Novartis
Education

Sri Indu Institute of Pharmacy
2013 - 2019Doctor of Pharmacy• SRI INDU INSTITUTE OF PHARMACY (JNTUH), HYDERABAD, INDIA Pursued Doctor of Pharmacy (PHARM.D) with an aggregate of 82% - 2019. CORE SUBJECTS: Pharmacology, Clinical research, Medicinal chemistry, Pharmacotherapeutics, Biostatistics and Research methodology.
Experience

Aware Gleneagles Global Hospitals
Jul 2017 - Jan 2018ObserverShadowed a variety of health professionals during their everyday routines.Assisted in collecting / confirming demographic information of patients in (E-Medra) EMR system for accurate patient tracking.Participated in ICU and ward rounds.Managed the follow up of patient cases from admission to discharge.Conducted inventory management to ensure proper tracking and ordering of needed supplies.

Clinwave Research Pvt Ltd
Jan 2019 - Apr 2021Clinical Research Associate• Performing the Site Initiation, Monitoring and Close-out Visits. • Execute trials as per ICH-GCP guidelines and SOP of the Organization.• Reviewing the Trial procedures on sites to minimize the errors that profound during the trial.• Review trial procedures to minimize errors• Preparing the Clinical Trial Agreement between the CRO, Principal Investigator and Site (SMO)• Maintaining all the documents pertaining to the trial in Trial Master File.• Report any amendments to the Site Personnel for Ethics Committee with in the trial duration.• Manage and prepare source templates as per Study design in accordance with the CRF, provided by the sponsor. Show less

IQVIA India
May 2021 - Aug 2022Associate Central Monitor1) Complete appropriate role-specific training to perform job duties.2) Perfroms assigned tasks to support team members with project execution (examples of such tasks include but not limited to running system reports, preparing and distributing status reports, creating and maintaining study documents, etc.)3) Interact with Sites / Clinical Research Asssociate and follow-up of missing data, pending queries, source data verification backlog, visit schedule, protocol deviations, etc.4) Assist in preparation of i-site pack for respective sites and countries for assigned studies.5) Perform the activities as per the task list delegated by Centralized Monitoring Specialist / Centralized Monitoring Lead.6) Assist in updating and maintaining data in systems within project timelines and per project requirement.7) Establish and maintain effective project / Site Communication.8) Create and maintain relevant project documents.9) Ensure accurate completion and maintenance of internal systems, databases, tracking tools and project plans.10) Act as a backup for Centralized Monitors. Show less

Novartis
Aug 2022 - nowClinical Research Associate
Licenses & Certifications

Clinical Trial Programming ( Base SAS Advanced SAS Clinical SAS)
IDDCRMay 2021- View certificate

Communicating with Emotional Intelligence
LinkedInOct 2021 - View certificate

Project Leadership
LinkedInNov 2021 - View certificate

Remote Work Foundations
LinkedInSept 2021 
Certificate Course in Drug Regulatory Affairs (DRA)
UdemyJun 2022- View certificate

Proven Tips for Managing Your Time
LinkedInAug 2021 - View certificate

Interpersonal Communication
LinkedInJun 2021 - View certificate

Efficient Time Management
LinkedInJun 2021 - View certificate

Mental Health Studies
AlisonAug 2020
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