HARSH PATEL
Calgary
Summary
Highly knowledgeable in fundamental chemistry concepts, including equilibrium, kinetics, thermodynamics, chemical bonding, and atomic structure. Proficient in hands-on laboratory procedures such as titrations, spectroscopy, chromatography, and safe chemical handling. Cultivates critical thinking abilities to assess experimental findings, scientific literature, and chemical phenomena. Skilled in effectively conveying scientific ideas through presentations and written reports. Proven track record as a professional researcher with expertise in conducting and analyzing scientific studies. Experienced in data collection, statistical analysis, and technical writing. Recognized for strong collaboration within teams, adaptability, and consistently delivering impactful results. Exceptional at managing multiple projects and meeting deadlines with precision and efficiency.
Overview
3
3
years of professional experience
Work History
Research associate
Veeda Clinical Research
03.2023 - 12.2023
- Performed and executed laboratory techniques as per methods independently, following the company’s Standard Operating Procedures (SOP) to carry out analyses
- Ensure that the validation plan outlines the target scope (such as the range of analyte concentrations and matrices) and the objective of the method validation (such as accuracy, precision, specificity, etc.) explicitly
- Verify that the validation methodology has a defined experimental design (number of replicates, controls, etc.) and the right statistical techniques and acceptance criteria
- Verify procedures for sample collection, storage, preparation, and analysis to ensure they are appropriate and documented
- Determine that the study plan includes the necessary quality control methods (such as calibration standards and QC samples) to guarantee the validity and dependability of the results
- Examine the completeness, accuracy, and traceability of raw data, such as chromatograms, spectra, and other analytical data, by verifying their integrity
- Make sure that all experiments are consistent by comparing the raw data to the predicted results
- Find and examine any unusual outcomes or procedure deviations that are recorded in the raw data
- Maintained cleanliness by making sure all equipment, tools and materials are cleaned
- Proficient in applying Good Manufacturing Practice (GMP) and regulatory requirements to ensure compliance with company’s standards and requirements
Analyst and Senior Analyst
Cliantha Research
10.2020 - 02.2023
- Company Overview: (Bio-analytical Lab)
- Assure correct sample handling to preserve integrity and avoid contamination
- Check to see if transportation, storage, and collection procedures are being followed
- Analyse whether the liquid-liquid extraction (LLE), solid-phase extraction (SPE), or protein precipitation (PPT) techniques are appropriate and validated for the particular analytes in plasma, urine, or blood
- Examine the calibration procedures for pipettes that are used once and again
- Make that they abide by the guidelines provided by the manufacturer, global standards, and legal requirements
- Analyse the accuracy and manner of preparation of the stock solutions
- Follow Good Laboratory Practice (GLP) for stability testing and appropriate storage conditions
- Verify the working solution preparation procedure, taking note of the dilution factors and computations
- Make sure the concentration is accurate and consistent before using it for sample analysis
- Examine documentation procedures to make sure they abide by GDP regulations
- This entails keeping thorough records of the techniques used for sample preparation, extraction, calibration, and data processing
- Make that sample handling and extraction practices follow GCP requirements for clinical research
- This covers protocol adherence, informed consent, and ethical issues
- Check to see if the lab meets GLP requirements for research using bioanalysis
- This covers equipment calibration, maintenance, validation, and facility organisation
- Check if BA-BE study compliance with regulatory regulations (such as FDA and EMA) is being met
- Make sure that the pharmacokinetic data's accuracy and repeatability are supported by the extraction techniques
- (Bio-analytical Lab)
Education
M.sc - Chemistry
KSV
Gujarat04.2019
B.sc - Chemistry
Gujarat university
Gujarat06.2016
Skills
- GLP
- GCP
- WHMIS
- Team collaboration
- Communication & Organization Skills
- Computer Literacy
- Calibration of micro pipette
- Single pipette
- Repeat pipette
- TLC
- PH
- Titration
- Ion Exchange Chromatography
- HPLC
- GC
- Analytical method validation
- Method development
- Analysis of data
- Reporting
- Microscopy
- Aseptic technic
- Extraction of LLE
- SPE
- PPT methods
- Data interpretation
- Scientific writing
- Research and analysis
- Data collection
- Quantitative research
- Laboratory techniques
- Research planning
- Qualitative research
- Clinical research
- Lab safety
- Computer programming
- Ethics compliance
Languages
English
Professional Working
Hindi
Full Professional
Gujarati
Native or Bilingual
Instrument Skills
- Calibration of micro pipette, Single pipette, repeat pipette.
- Able to perform various analytical techniques: TLC, pH, Titration, Ion Exchange Chromatography, HPLC, GC, Calibration etc.
- Perform Sample and Standard Preparation as per analytical methods, GMP, SOPs, and safety regulations.
- Knowledge of analytical method validation, method development Analysis of data and reporting.
- Carried out medical laboratory procedures using skills in microscopy, microbiology, aseptic technique.
- Perform extraction of LLE, SPE, PPT methods.
Timeline
Research associate
Veeda Clinical Research
03.2023 - 12.2023
Analyst and Senior Analyst
Cliantha Research
10.2020 - 02.2023
M.sc - Chemistry
KSV
B.sc - Chemistry
Gujarat university
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