Laurin Khan Email & Phone Number

-Oversee project delivery process of global Phase II-III clinical trials from startup to closeout, serving as primary point of contact with Clients.-Manage all project activities, resources, and budgets to ensure successful completion of studies and key performance indicators are met.-Contribute to clinical development activities such as protocol, protocol amendment, and ICF writing. -Support process improvement initiatives and provided input into strategic direction for protocol level activities.-Implement robust risk management strategies, identified potential issues and developed mitigation strategies early to minimize disruptions to study operations.-Ensure studies are conducted in compliance with GCP, relevant SOPs, and regulatory requirements.-Provide oversight for development and implementation of project plans across functional areas.-Responsible for maintaining quality and completeness of TMF for all assigned projects.

-Managed all aspects of global Phase II-IV clinical trials from startup to closeout. -Conducted laboratory database setup for clinical trials, ensuring compliance with protocol requirements. -Regularly interfaced with Clients to report study status, ensuring project milestones and deliverables were met on-time, while actively performing quality assurance and risk management activities to maintain project quality. -Managed project budgets to monitor that billing spend does not exceed the allocated budget.-Developed and implemented the Project Management Plan for assigned studies.

Duarte, California, United States

-Led Phase I First-in-Human oncology trials (multiple myeloma), both sponsor-driven and investigator-initiated trials. -Assisted Principal Investigators, Sub-Investigators, and Clinical Research Nurses with the informed consent process and confirming patient eligibility. -Completed and maintained accurate data collection in electronic case report forms (eCRF)-Submitted serious adverse events, unanticipated problems, and protocol deviations to regulatory authorities as appropriate.

-Managed multiple global Phase II-IV clinical trials of various general medicine indications as lead study coordinator.-Completed and maintained accurate data collection in electronic case report forms (eCRF).-Interfaced with study participants to complete study visits per protocol.