Shailja Chandel
Clinical Research Professional
- Role
- Clinical Operations Specialist at IAVI
- Location
- New York, NY, US
- LinkedIn followers
- 500 followers
About Shailja Chandel
Experienced Clinical Operations Specialist with 12+ years in clinical research, skilled in managing multi-site trials from initiation to closeout. Proficient in site selection, developing and reviewing study documents and plans (protocols, ICFs, eCRFs, monitoring, communication, document management, vendor management plans, etc.), protocol execution, data integrity, regulatory compliance, and cross-functional coordination. Hands-on experience in monitoring and central IRB management.
Experience
Clinical Operations Specialist
Nov 2022 — Present · New York, NY, US
Education
Himachal Pradesh University , Shimla
Bachelor of Science (B.Sc.), Biotechnology
Cliniminds
Postgraduate Diploma, Clinical Research and Clinical Data Management
Monal Public School, Shimla
+2
Skills
- Knowledge of Ich- Gcp Guidelines
- Pharmaceutical Industry
- Sop
- Crf Design
- Protocol Designing
- CRO
- Standard Operating Procedure (Sop)
- Clinical Trials
- Clinical Data Management
- Clinical Research
- Good Clinical Practice (Gcp)
- Informed Consent
- Ich-Gcp
- Biotechnology
- Regulatory Affairs
- Project Planning
- Clinical Development
- Protocol
- Schedule Y
- Microsoft Office
- Life Sciences
- CRO Management
- Gcp
- Principles of Pharmacology
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