Parvesh SinghRangra
@parveshsinghrangra
Clinical Data Scientist with 4+ years' oncology and vaccine clinical data management experience.
What I'm looking for
I am a Clinical Data Scientist with over four years of progressive experience in clinical data management across oncology, vaccine, respiratory, and neurology studies. I have supported end-to-end CDM activities from study setup through database lock and closeout, working with eCRFs, third-party data and SAE reconciliation.
I have applied data quality frameworks, developed Data Quality Plans (DQP/DQPM), performed UAT, and prepared study status reports and listings to support clinical teams. I have hands-on experience with Medidata Rave, Oracle Clinical, RDC, and other clinical data systems.
Throughout my roles I have managed lab data integration and reconciliation, executed advanced data cleaning and query resolution, and contributed to training and process documentation. I routinely ensure SOP and GCP compliance and support inspections, audits and database validation activities.
I seek to deliver accurate, high-quality clinical data to enable timely, compliant study decisions and improved patient safety, while continuing to expand my technical and trial leadership capabilities.
Experience
Work history, roles, and key accomplishments
Provided data management input and performed DM activities for study start-up, UAT, data reconciliation and ongoing data review for clinical trials including COVID-19 studies; developed proposals and listings to resolve data issues and generated study status reports for trial teams.
Clinical Data Associate II
Thermo Fisher Scientific
Apr 2023 - May 2025 (2 years 1 month)
Performed advanced data cleaning, SAE and third-party vendor reconciliation, generated and resolved data queries, and produced project-specific status reports to ensure data accuracy and compliance with GCP and SOPs.
Clinical Data Associate
Tech Observer
Dec 2021 - Mar 2023 (1 year 3 months)
Managed project document control, DMTMF/e-filing, CRF review and UAT coordination; created and tracked data clarification forms and performed basic QC to maintain data validity and SOP compliance.
Associate Clinical Research
Artemis Hospital
Feb 2021 - Nov 2021 (9 months)
Coordinated clinical trial activities including informed consent, subject recruitment and follow-up, lab coordination, IP handling, AE/SAE reporting, monitoring visit support and trial documentation in compliance with GCP.
Education
Degrees, certifications, and relevant coursework
Sardar Bhagwan Singh Post Graduate Institute of Biomedical Sciences & Research
Bachelor of Pharmacy, Pharmacy
2015 - 2019
Completed a Bachelor of Pharmacy degree with coursework and training in pharmaceutical sciences and clinical trial-related practices.
Tech stack
Software and tools used professionally
Availability
Location
Authorized to work in
Job categories
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