Preeti Singh
About Preeti Singh
Preeti Singh is a Clinical Trials Associate at Bristol Myers Squibb in Melbourne, Australia, with extensive experience in clinical research and trials management.
Title
Preeti Singh is currently serving as a Clinical Trials Associate at Bristol Myers Squibb in Melbourne, Victoria, Australia. Her experience encompasses various roles in the clinical research field, demonstrating a diverse skill set and deep industry knowledge.
Professional Experience
Preeti Singh began her career as a General Dentist at Jaipur Dental College in Jaipur, India. She transitioned to Excel Life Sciences Pvt. Ltd. where she served as a Clinical Trial Assistant and then as a Clinical Research Coordinator in New Delhi. She later joined Kings Langley Dental Surgery as a Dental Assistant in Sydney, Australia. From 2019 to 2021, she worked with PCI Pharma Services as a Clinical Trials Logistics Associate before her current role at Bristol Myers Squibb.
Educational Background
Preeti Singh earned her Bachelor’s Degree in Dental Surgery (BDS) from Rajasthan University of Health Sciences, Jaipur. Following this, she completed a diploma in clinical research and pharmacovigilance from ICRI. Her educational background has provided a strong foundation for her career in clinical research and trials.
Clinical Trials Expertise
Preeti Singh has substantial expertise in managing clinical trials, including handling site feasibility, start-up, ethics submission, and study close-out processes. She has managed four different studies and organized study visits for over 70 patients, maintaining Trial Master Files (TMF) and recording data on electronic Case Report Forms (eCRF).
Skills and Specializations
Preeti Singh possesses robust skills in various aspects of clinical trials, such as regulatory affairs, feasibility assessment, data monitoring, SOP drafting, statistical analysis, adherence to ICH/GCP guidelines, and CTMS management. She is also proficient in protocol designing, EDC, study start-up and close-out operations, coordinating with Clinical Research Associates (CRAs), managing eCRFs, and informed consent forms.