Vishvas Patel
Edmonton,Canada
Summary
Results-oriented and detail-driven clinical research professional with a strong background in protocol adherence, data integrity, and regulatory compliance. I am seeking a challenging role as a Clinical Research Coordinator. Where I can leverage my three years of experience to contribute to the success of innovative clinical trials. I am dedicated to ensuring the highest standards of ethical conduct and playing a key role in advancing healthcare solutions.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Pharmacy Assistant Team Lead
Bayshore Specialty RX
01.2023 - Current
- Provide training to new team members and develop and revise SOP for IV preparation
- Assists the pharmacist in preparing required infusion supplies for delivery of medication, Assists the pharmacist in programming pumps and infusion devices for medication delivery
- Communicate with the insurance company and resolve issues related to drug benefit
- Assists the pharmacist in entering prescriptions into the prescription software (Kroll), and filling/billing such prescriptions
- Collecting ADR and reporting ADR to the Bayshore PV department in 24 hr
Clinical Research Coordinator (Dermatology/Cardiovascular/Cancer)
Clianta Research Limited
11.2019 - 12.2022
- Study Coordination: oversee the day-to-day operations of clinical trials, ensuring compliance with protocols, regulations, and ethical standards
- Participant Recruitment: Actively recruiting and screening eligible participants for clinical trials, explaining the study procedures and obtaining informed consent
- Data Collection and Management: Collecting and documenting study data accurately, maintaining records, and ensuring data integrity
- Protocol Adherence: Ensuring that all study procedures are conducted according to the approved protocol and regulatory requirements
- Communication: Serving as a liaison between study participants, investigators, sponsors, and regulatory agencies, providing updates and addressing concerns
- Safety Monitoring: Monitoring participant safety throughout the study, reporting adverse events, and following up as necessary
- Regulatory Compliance: Maintaining regulatory documents, obtaining necessary approvals, and ensuring compliance with institutional and regulatory guidelines
- Quality Assurance: Implementing quality control measures to ensure the accuracy and reliability of study data
- Study Close-Out: Coordinating study close-out activities, including data analysis, reporting, and archiving of study documents
Education
CLINICAL RESEARCH, DRUG SAFETY AND PHARMACOVIGILANCE -
ACADEMY OF APPLIED PHARMACEUTICALSCIENCE
Toronto, ONTARIO08.2018
PHARM D -
K.B. INSTITUTE OF PHARAMCUTICAL EDUCATION AND RESEARCH
GANDHINAGAR, INDIA05.2017
BUSINESS MANAGEMENT LEVEL 1 -
MIDDLESEX UNIVERSITY LONDON
LONDON, ENGLAND01.2011
Skills
- Knowledge of regulations and guidelines
- Project management skills
- Interpersonal skills
- Attention to detail
- Data collection
- Electronic Data Capture
- Safety Reporting
Certification
- Clinical Research Regulation and Good Clinical Practice (GCP), 2017
- Legislation, guidelines and Ethics in Clinical Research and drug safety, 2017
- Pharmacovigilance Regulation and good Pharmacovigilance Practices (GVP), 2017
- Medical Device safety and clinical trial, 2018
- GCP And GVP inspection and Audits, 2018
- SCORA, 2018
- Project Management, 2018
Publications
- Clinical Similarity of Biosimilars and Reference Drugs: A Comprehensive Review and New Hope for Public Health in a New Frontier, Curr Drug Res Rev, 11/02/23, 10.2174/0125899775246113231018080526
- Unveiling the modulation of Nogo receptor in neurodegeneration and plasticity: Novel aspect and future horizon in new frontier, Biochemical Pharmacology, 02/23, 10.1016/j.bcp.2023.115461
- Revamping the innate or innate-like immune cell-based therapy for hepatocellular carcinoma: new mechanistic insights and advanced opportunities, Med Oncol, 01/21/23, 10.1007/s12032-023-01948-4
- Assessment of potential drug-drug interactions among outpatients in a tertiary care hospital: focusing on the role of P-glycoprotein and CYP3a4 (retrospective observational study), HELIYON, 10/27/22
- Emerging Pathophysiological Mechanisms Linking Diabetes Mellitus and Alzheimer’s Disease: An Old Wine in a New Bottle, 01/01/22
- Triple-negative breast cancer management: A review of conventional and contemporary treatment strategy, Future Journal of Pharmaceutical and Health Study, 2022
- Medication knowledge and its effect on Biochemical laboratory parameters, Indian Journal of Applied Research, 03/2021
Languages
English
Full Professional
Timeline
Pharmacy Assistant Team Lead
Bayshore Specialty RX
01.2023 - Current
Clinical Research Coordinator (Dermatology/Cardiovascular/Cancer)
Clianta Research Limited
11.2019 - 12.2022
PHARM D -
K.B. INSTITUTE OF PHARAMCUTICAL EDUCATION AND RESEARCH
BUSINESS MANAGEMENT LEVEL 1 -
MIDDLESEX UNIVERSITY LONDON
- Clinical Research Regulation and Good Clinical Practice (GCP), 2017
- Legislation, guidelines and Ethics in Clinical Research and drug safety, 2017
- Pharmacovigilance Regulation and good Pharmacovigilance Practices (GVP), 2017
- Medical Device safety and clinical trial, 2018
- GCP And GVP inspection and Audits, 2018
- SCORA, 2018
- Project Management, 2018
CLINICAL RESEARCH, DRUG SAFETY AND PHARMACOVIGILANCE -
ACADEMY OF APPLIED PHARMACEUTICALSCIENCE
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