Tejaswi Appalarowthu

Angestellt, Clinical Data Manager, University Hospital, Ludwig-Maximilians-Universität (LMU)

München, Deutschland

Fähigkeiten und Kenntnisse

Rave
Inform
OC-RDC
Project Management
DSG eCaselink
Adobe InDesign
CRF Designing
ICH-GCP
Clinical Trails
Clinical Research
CRO Management
Clinical Pharmacy
Good Clinical Practice
Life Sciences
User Acceptance Testing
Protocol
Standard operating procedure
Clinical Data Management
SAS (basics)
Data Quality Control
Review Edit Checks
Data Validation
SAE Listings
SAE Reconciliation
Medical Coding
CRF Design
DSG ecaselink
DB Startup/DB Lock
Data Cleaning
Status Reports
Client/Vendor Management
SAS Listings/Review/Validation
Oncology
Neurology
Gastroenterology
Diabetes
Audiology
Hold German Job Seeker Visa
Open for jobs based in any city within Germany
CDISC Standards
SDTM and AdAM
TLFs
Statistical Programming
eCRF design
EDC system set up
Data coding
Query generation
Data Review
Database release
Data validation plans and other study specific pro
Medidata Rave
Monitoring
Englische Sprache

Werdegang

Berufserfahrung von Tejaswi Appalarowthu

  • Bis heute 4 Jahre und 4 Monate, seit Feb. 2020

    Clinical Data Manager

    University Hospital, Ludwig-Maximilians-Universität (LMU)

  • 7 Monate, Nov. 2018 - Mai 2019

    Clinical Data Coordinator 1

    Navitas Life Sciences

    Experienced Clinical Data Manager with a demonstrated history of working in the pharmaceuticals industry. Skilled in Clinical Research, Validation, Clinical Trials, and Good Clinical Practice (GCP). Proficient in all data management activities (Start-up, Conduct, and final lock) and strong understanding of regulatory procedures. Successfully managed studies over Electronic Data Capture like Medidata Rave, Inform, DSG eCaselink, OC-RDC etc.

  • 3 Jahre und 7 Monate, Mai 2015 - Nov. 2018

    Clinical Data Specialist

    IQVIA

  • 1 Jahr, Apr. 2014 - März 2015

    Research Associate

    Core Clinical LLC

    • Active participation on project management understanding process through – protocol study design, CRF Development research deliverables and methodologies [regulatory environment – CDSCO, USFDA].

Ausbildung von Tejaswi Appalarowthu

  • 2 Jahre und 1 Monat, Juni 2011 - Juni 2013

    Mpharmacy

    Rajiv Gandhi University of Health Sciences

    Pharmacology

  • 4 Jahre, Juni 2007 - Mai 2011

    BPharmacy

    Acharya Nagarjuna University

Sprachen

  • Deutsch

    Grundlagen

  • Englisch

    Fließend

Interessen

German language(A2 Level)
SAS Programming
Reading books
Listening music
Gardening

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