SAHER ZAIDI
Shrewsbury,USA
Summary
Experienced with coordinating research studies and managing project timelines. Utilizes organizational skills and attention to detail to ensure accuracy and compliance. Knowledge of data collection methodologies and participant engagement strategies.
Overview
13
13
years of professional experience
Work History
Data Review Assistant
Charles River Laboratories
06.2023 - 06.2025
- Collaborate with chemists and principal investigator scientists to understand data requirements and expectations for individual clinical studies
- Safeguarded sensitive information through proper documentation handling, data entry, and record maintenance procedures.
- Improved data management by creating comprehensive databases for easier access to critical information.
Data Analyst/Program Coordinator
R-Research Endocrinology Clinic/IMI Worldwide
01.2020 - 05.2023
- Monitored performance metrics closely to evaluate areas requiring intervention or adjustment, making data-informed decisions that contributed positively towards overall results
- Collaborating with global social work teams to produce a quarterly medical newsletter, involving outreach and research for multiple global social/clinical projects
Research Coordinator
Journey to Wellness, Inc.
01.2019 - 06.2019
- Implementation of data interface connecting all local substance abuse clinics for purpose of streamlining data collection and management processes
- Conducted independent practicum research study field research, collecting samples, and documenting data.
- Managed patient recruitment, informed consent process and data entry to support trial objectives.
Clinical Supply Specialist
PAREXEL International
09.2013 - 08.2017
- Conducted regular audits of inventory levels to identify discrepancies and implement corrective measures promptly.
- Spearheaded the adoption of new technology to improve tracking and management of clinical supplies.
- Liaised with other healthcare facilities during times of need, coordinating resource sharing and support to maintain optimal patient care.
Clinical Logistics Assistant
PAREXEL International
05.2012 - 09.2013
- Prepared reports tracking information such as purchase orders, inventory numbers, and invoicing activities.
- Managed purchase order processing from initiation to completion, verifying accuracy at each stage to prevent errors or delays in fulfillment using clinical trial management systems (CTMS)
Education
Master of Science - Epidemiology and Biostatistics
University of Massachusetts
Amherst, MA05-2021
Post Graduate Diploma - Clinical Research and Regulatory Affairs
Toronto Institute of Pharmaceutical Technology (TIPT)
Toronto, Ontario01.2010
Bachelor of Science - Neuroscience and Health Studies
University of Toronto
Toronto, Ontario06-2008
Skills
- Regulatory Comprehension (IRB, GCP, NDA)
- Patient Recruitment/Enrollment
- Stata (Statistical Analysis Software)
- Detailed oriented, organization skills
- Strong interpersonal communication skills
- Ability to multitask and manage time efficiently
- Data organization, collection, analysis
- Research design, experimental design
- Qualitative research, quantitative research
- Scientific writing, report preparation
- Project oversight
- Quality assurance
Timeline
Data Review Assistant
Charles River Laboratories
06.2023 - 06.2025
Data Analyst/Program Coordinator
R-Research Endocrinology Clinic/IMI Worldwide
01.2020 - 05.2023
Research Coordinator
Journey to Wellness, Inc.
01.2019 - 06.2019
Clinical Supply Specialist
PAREXEL International
09.2013 - 08.2017
Clinical Logistics Assistant
PAREXEL International
05.2012 - 09.2013
Master of Science - Epidemiology and Biostatistics
University of Massachusetts
Post Graduate Diploma - Clinical Research and Regulatory Affairs
Toronto Institute of Pharmaceutical Technology (TIPT)
Bachelor of Science - Neuroscience and Health Studies
University of Toronto
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