Accomplished Clinical Research Associate from Lambda Therapeutic Research Ltd, adept in project management and protocol development. Excelled in coordinating site operations, enhancing data collection processes, and leading team training initiatives. Demonstrated proficiency in MS Office, ensuring meticulous report writing and regulatory compliance. Proven track record in improving clinical research outcomes through strategic planning and effective communication.
Overview
5
5
years of professional experience
Work History
Clinical Research Associate
Lambda Therapeutic Research Ltd
12.2018 - 12.2023
Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
Perform sample separation procedures such as centrifugal, aliquoting, and labeling to prepare samples for storage or analysis.
Adhered to procedures, practices and regulatory requirements to maintain health, safety and environmental compliance.
Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues.
Created and maintained database and records filing system to document data on specimen collection, processing and storage.
Liaised with Bio-analysis department personnel to communicate important clinical data and events.
Supported development and delivery of department training to maximize success of clinical research.
Followed Sample storage procedures to comply with protocols and SOP requirements.
Education
Master of Science - Biotechnology
KSV University
India
05.2018
Bachelor of Science - Biotechnology
HNGU University
India
05.2016
Skills
Coordinating site operations and audit coordination
Report Writing and Completing regulatory documents
Sample development
Project Management
Data Collection
GMP
Team Training
Protocol development
Proficient in MS Office
Timeline
Clinical Research Associate
Lambda Therapeutic Research Ltd
12.2018 - 12.2023
Master of Science - Biotechnology
KSV University
Bachelor of Science - Biotechnology
HNGU University
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