Mai Tran, Mpa Email & Phone Number

Menlo Park, Ca, Us

In partnership with scientific leadership, established the company's first Real World Evidence program with several large-scale clinical studies; lead executional strategy of programs under aggressive timelines and program goals; key contributor to regulatory and commercial strategies; serve as the cross-functional lead for multiple programs working closely with clinical, technical, and commercial teams and ensuring alignment with company goals.

Menlo Park, Ca, Us

Served as the program lead for the first implementation and return of results, large-scale interventional study for multi-cancer early detection, which provided the clinical evidence to support the launch of the GRAIL's first commercial product, Galleri. Also established the company's first compassionate use, expanded access study to provide multi-cancer early detection testing to patients in need; led several other strategic work streams which required cross-functional team management and reporting to executive leadership.

Menlo Park, Ca, Us

Served as the program lead for several programs, including a large-scale multi-cancer early detection screening study of 100,000 participants; responsible for cross-functional management of program concept through execution; lead R&D and clinical development work streams.

As the only clinical operations personnel, managed two global Phase I/II studies in pediatric adrenoleukodystrophy (study was conducted in 5 continents) and a natural history study in the US for a stealth start-up environment- Managed multiple CROs (global and local) and vendors (e.g., lab, imaging, data)- Led the development of public relations and social media platforms for both studies- Co-developed partner identification strategy and led the site selection process for both studies

South San Francisco, Ca, Us

- Managed global Phase 2 programs in ultra-rare autoimmune indications; oversee study budgets, timelines, enrollment forecasting, data quality and review, and regulatory aspects of study conduct in accordance with GCP ad ICH guidelines.- Contributed to the company’s first NDA filing and managed critical components of BIMO inspections with favorable results-Cross-functionally managed special projects within Clinical Development meeting goals of the company

San Francisco, California, Us

Directly managed a 90+ member team in clinical operations across three hospital sites for 14 clinical research programs, including a Phase I research unit. Operationalized over 700 clinical trials across four departments in the Cancer Center and School of Medicine. Collaborated with 12 department Chairs and over 50 principal investigators. Rebuilt the clinical research team into a well-trained group to effectively and safely manage the care of cancer patients in clinical trials. Collaborated with hospital administrators to streamline workflow and solve operational challenges. Served as the escalation point for study Sponsors, auditors, department Chairs, and patients. Served as one of the Cancer Center's lead for FDA inspections for clinical trials.

Palo Alto, California, Us

Director on the Board of an organization which fosters opportunities for cross-cultural understanding between the U.S. and Asia

- Managed intervention studies of the "Live Healthy and Live Long" Program which utilizes community-based participatory research to promote and increase colorectal cancer screening in the Vietnamese-American community.- Managed and promoted Health Research Partnerships in Asian Communities, a program to increase community-engaged health research.- Responsible for the operational oversight of programs, projects, and research staff, including grants management (NIH and foundation grants)

Stanford, Ca, Us

- Coordinated clinical trials in the Division of Hematology, with a focus in myelodysplastic syndromes (MDS); Executed industry-sponsored and cooperative Phase I, II, and III studies.- Managed patient treatment plans in collaboration with physicians, nurses, and healthcare staff - Managed research studies from protocol proposal and initiation, budget planning, quality assurance throughout phase of trial, to study closure. - Ensured accuracy of data and compliance for human subjects research per GCP, ICH and local Institutional Review Board policies. Wrote and submitted applications, renewals, and reports to local IRB and FDA. - Maintained positive and trusting relationships with all patients and their families.

Oakland, California, Us

Coordinated clinical research trials in oncology, mainly with breast, prostate, lung, and brain cancers. Worked closely with healthcare staff to implement treatment plan for patients. Managed data and assured quality and accuracy.

Office of Disaster Medical Services: Assisted the planning and implementation process for mass medical emergencies response within the County. Managed fiscal database; managed outside contracts with County contractors and vendors.

Interviewed tuberculosis patients within Santa Clara County to assess missed opportunities and disparities in health care. Interviewed patients in both English and Vietnamese; collected participant data while ensuring participant confidentiality and data integrity. Collaborated with nurse case managers, Communicable Disease Control Dept., and State Health Department in collection and analysis of data.

Masters, Public Administration

Bachelors, Molecular, Cellular, Developmental Biology