Jasmine Dhaliwal

About Jasmine Dhaliwal

Accomplished Senior Clinical Trials Associate with more than 8 years of experience in the pharmaceutical sector, specializing in oncology trials. Proficient in managing clinical trials, ensuring compliance with regulations, and developing protocols. Currently focused on safety reporting and Individual Case Safety Reports (ICSRs). Demonstrated ability to collaborate with diverse teams to ensure trials are executed and completed on schedule. Skilled in using various clinical trial management systems (CTMS) and electronic data capture (EDC) tools. Well-versed in GCP guidelines and regulatory requirements. Seeking an opportunity to apply my expertise in a progressive organization dedicated to advancing healthcare solutions.

Experience

1. Clinical Research Specialist Ii

   N-Power Medicine, Inc.

   Mar 2026 — Present

   Serve as the Company’s trusted face to the clinical practice, providing clinical support while advancing research data collection-Interface directly with the healthcare providers and patients-Perform peer review of clinical documentation for data quality and completeness-Partner with Senior CRS to address any clinic or team issues and concerns-Obtain informed consent for N-Power Medicine’s clinical trials-Assist and participate in the site clinical trial initiation and clinical trial(s) activities as assigned-Ensure adherence to study protocols, data completeness and patient consent-Assist in patient recruitment strategies where appropriate-Foster collaborative relationships by effectively communicating with clinical site staff, internal stakeholders, and the N-Power Medicine team by attending site specific meetings-Build and maintain relationships at the clinical site, becoming part of the functional team of practitioners-Ensure quality and integrity of data capture, compliance and confidentiality with N-Power Medicine’s and site’s policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP)-Respond to queries regarding missing, aberrant, or potential outlier data and data verification- escalate to the health care provider as necessary for resolution-Provide proactive input and user experiences for our software. Additional duties and responsibilities as required.

Skills

• Microsoft Office
• Adobe Creative Suite
• Mac Os
• International & Domestic Shipping
• Customer Service
• Receptionist Duties
• Office Administration
• Social Networking
• Ios
• Freight Forwarding
• Air Freight
• Freight
• Ocean Freight
• Customs Regulations
• International Logistics
• Logistics Management
• Logistics
• Shipping
• Transportation
• Warehousing
• Ocean
• Export
• 3pl
• Container
• Import
• Import Export
• Forwarding
• Supply Chain Management
• Transportation Management
• Clinical Operations
• Clinical Trial Management System (Ctms)
• Clinical Research
• Clinical Trials
• Good Clinical Practice (Gcp)
• Clinical Data Management