Pijush Majumdar
Winnipeg,Canada
Summary
Detail-oriented and highly motivated medical professional with a strong foundation in clinical research and over 10 years of experience in managing patient care operations and drug development, seeking to secure a clinical research coordinator role to contribute to advancement of medical research and patient care. Expertise in developing and implementing effective operational strategies that ensure compliance with FDA safety regulations, alongside a strong track record in data analysis, project management, budgeting, process improvement and optimization. Exceptional interpersonal, organizational, and problem-solving skills facilitate effective collaboration with cross-functional teams to achieve operational excellence.
Overview
17
17
years of professional experience
1
1
Certification
Work History
Study group participant
McMaster University
Hamilton, Canada
09.2023 - Current
- Proficient in ensuring adherence to FDA guidelines, ICH-GCP standards and other relevant regulatory requirements throughout the entire research process
- Skilled in utilizing Electronic Data Capture (EDC) systems and proficient in data entry, validation and maintenance to ensure accuracy and integrity of research data
- Proven track record of successfully identifying, screening and enrolling eligible participants while maintaining high retention rates through effective communication and rapport-building
- Demonstrated ability to develop, implement and oversee detailed study protocols, ensuring accurate data collection and participant safety
- Proficient in coordinating all aspects of clinical trials, including scheduling participant visits, managing investigational products and overseeing study timelines
- Knowledgeable in timely identification, documentation and reporting of adverse events, ensuring compliance with regulatory reporting requirements
Pharmacy manager
Wal-Mart Pharmacy
Winnipeg, Canada
07.2021 - Current
- Evaluated patient records for accuracy, completeness, appropriateness of medication therapy, potential drug-drug interactions, allergies or contraindications
- Collaborated with physicians, nurses and other healthcare providers to optimize patient outcomes through evidence-based medicine protocols
- Ensured compliance with state board regulations by regularly auditing prescription files for accuracy
- Led team meetings to discuss current performance objectives, set new goals and review progress towards achieving organizational goals
- Maintained knowledge of current industry standards concerning pharmaceutical regulations, laws and guidelines
- Provided training, guidance and support to pharmacy staff on the proper use of medications and drug interactions
- Maintained collaboration between governing boards, medical staff, and department heads by attending board meetings and coordinating interdepartmental functioning
- Administered fiscal operations, including accounting, planning budgets, authorizing expenditures, and establishing rates for services
Pharmacy manager
Rexall Pharmacy
Winnipeg, Canada
07.2009 - 06.2021
- Evaluated patient records for accuracy, completeness, appropriateness of medication therapy, potential drug-drug interactions, allergies or contraindications
- Collaborated with physicians, nurses and other healthcare providers to optimize patient outcomes through evidence-based medicine protocols
- Ensured compliance with state board regulations by regularly auditing prescription files for accuracy
- Led team meetings to discuss current performance objectives, set new goals and review progress towards achieving organizational goals
- Maintained knowledge of current industry standards concerning pharmaceutical regulations, laws and guidelines
- Provided training, guidance and support to pharmacy staff on the proper use of medications and drug interactions
- Maintained collaboration between governing boards, medical staff, and department heads by attending board meetings and coordinating interdepartmental functioning
- Administered fiscal operations, including accounting, planning budgets, authorizing expenditures, and establishing rates for services
Formulation Development Scientist
Patheon Inc.
Toronto, Canada
08.2007 - 08.2009
- Prepared reports summarizing information and trends related to manufacturing performance
- Estimated costs, production times, or staffing requirements for new designs
- Troubleshooted new and existing product problems involving designs, materials, and processes
- Incorporated new manufacturing methods and processes to improve existing operations
- Analyzed data from a variety of sources to identify trends in product performance and made recommendations for improvement
- Identified potential areas of improvement within existing processes through process mapping exercises
- Created protocols, reports and presentations summarizing experimental results for scientific meetings, regulatory filings and other stakeholders
- Maintained accurate records of all experimentations conducted in accordance with Good Laboratory Practices
- Conducted literature reviews to stay abreast of current industry developments within the field of drug development sciences
- Reviewed batch documentation prior to release ensuring accuracy according to cGMP regulations
- Managed and coordinated multiple projects while ensuring timely completion
- Collaborated with departmental leaders to establish organizational goals, strategic plans and objectives
Education
Post Graduate Diploma - Applied Clinical Research
McMaster University
CanadaMaster of Science (M.Sc) - Molecular Pathology
University of Western Ontario
CanadaBachelor of Science (B.Sc) - Pharmacy
University of Burdwan
IndiaSkills
- Regulatory compliance
- Data management
- Data analysis
- Protocol adherence
- Clinical trial coordination
- Attention to detail
- Effective communication
- Team collaboration
- Problem-solving
- Ethical awareness
- Adverse event tracking
- Informed consent
- Participant screening
- Study protocols
- Good clinical practice
- Report preparation
- Informed consent process
- Electronic data capture
- Adverse event reporting
- Clinical trial management
Publications
Leptin and endothelin-1 mediated increased extracellular matrix protein production and cardiomyocyte hypertrophy in diabetic heart disease., Diabetes Metabolism Research and Reviews. Pijush Majumdar, Shali Chen, Biju George, Subhrojit Sen, Morris Karmazyn, Subrata Chakrabarti.
Certification
- GCP for Clinical Trials with Investigational Drugs and Biologics (ICH focus)
- Good Clinical Practice (GCP)
- Transportation of Dangerous Goods (TDG/IATA)
Timeline
Study group participant
McMaster University
09.2023 - Current
Pharmacy manager
Wal-Mart Pharmacy
07.2021 - Current
Pharmacy manager
Rexall Pharmacy
07.2009 - 06.2021
Formulation Development Scientist
Patheon Inc.
08.2007 - 08.2009
- GCP for Clinical Trials with Investigational Drugs and Biologics (ICH focus)
- Good Clinical Practice (GCP)
- Transportation of Dangerous Goods (TDG/IATA)
Post Graduate Diploma - Applied Clinical Research
McMaster University
Master of Science (M.Sc) - Molecular Pathology
University of Western Ontario
Bachelor of Science (B.Sc) - Pharmacy
University of Burdwan
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