Clinical Trial / Who We Are / 
Our Staff


Linda Wu, RN, MsN, CCRC Phone: (909) 651-5002
Director of Operations, CTC E-mail: lwu@llu.edu

Ms. Linda Wu works under the auspices of institutional leadership to produce and implement the strategic plan for the Clinical Trial Center. She oversees administration in the areas of clinical trial contracting, financial management, site operation and training, as well as development and promotion.

Ms. Wu received her Master of Science in Nursing from the University of Minnesota in 1993. She has experience as a clinical research coordinator in various therapeutic areas, and as an administrator in both private practice as well as academic research settings. Ms. Wu’s career in clinical research extends domestically and internationally.

Lila Dalton, RN, BSN, CCRP Phone: (909) 651-5002
Associate Director of Operations, CTC E-mail: ldalton@llu.edu

Ms. Lila Dalton provides on-site trial management training and resources to clinical departments. She collaborates with clinical trial site personnel and ancillary service providers to ensure good procedural adherence and clinical trial progress. Furthermore, Ms. Dalton is involved in the advancement of pre-trial services as well as the training of junior staff.

Ms. Dalton has been a Registered Nurse since 1992 and is also certified as a Clinical Research Professional. She received her Bachelor of Science in Nursing from the University of Phoenix in 2011.  She has over thirteen years of experience in the clinical research field, with specialized practice in pediatrics and oncology. Her various roles within clinical research have encompassed nursing, coordination, and management.

Amy Casey, MBA, CRCP Phone: (909) 651-5002
Assistant Director of Clinical Trial Contracts, CTC E-mail: acasey@llu.edu

Ms. Amy Casey is responsible for reviewing, drafting, negotiating, and finalizing trial agreements and clinical confidentiality agreements. She provides training and interacts closely with faculty, staff, administration, students, and industry sponsors throughout the clinical trial agreement process.

In 2006, Ms. Casey received a Masters of Business Administration with an emphasis in Global Business from the University of Redlands. She has worked in the research administration setting for five years, with experience in the Office of Research Affairs, Office of Intellectual Property & Contracts, and most recently the Clinical Trials Working Group.

 

Michael Wilson, Jr., BS, MBA(c) Phone: (909) 651-5002
Senior Financial Analyst, CTC E-mail: miswilson@llu.edu

Mr. Michael Wilson, Jr. works in conjunction with Clinical Trial Center staff as well as university faculty and administration to manage clinical trial financials from commencement to close-out. His areas of responsibility include preparing financial documents, tracking and monitoring financials, responding to inquiries regarding study accounts, invoicing study sponsors, and distributing study compensations.

Mr. Wilson graduated in 2004 from California State University, Northridge with a Bachelor of Science degree in Systems and Operations Management. He is currently completing his Masters in Business Administration at Loma Linda University.  His professional repertoire incorporates over eight years of experience in project financial management, business and personal finance management, as well as commercial insurance billing administration.

 

Cindy Kronbeck

Cindy Kronbeck, LVN   Phone: (909) 651-5002
Research Coordinator, CTC     E-mail: ckronbeck@llu.edu

Ms. Cindy Kronbeck is a research coordinator for the Clinical Trial Center.  She is responsible for the facilitation, implementation and management of clinical trials managed by the Clinical Trial Center.  Ms. Kronbeck coordinates physician care, patient screening, recruitment, patient exams, investigational drug administration, consistent follow-up and documentation of patient’s medical experience, and accurate documentation of research data.

Cindy has been employed with Loma Linda University for over twenty years in various positions.  She has over five years of experience in the clinical research field, including PI-initiated and industry sponsored studies.

 

Megan Russell

Megan E. T. Russell, MA Phone: (909) 651-5002
Regulatory Affairs Coordinator, CTC E-mail: merussell@llu.edu

Mrs. Megan Russell coordinates study regulatory submissions for clinical research projects managed by the Clinical Trial Center.  She is responsible for assisting the PI in the creation and maintenance of all regulatory documentation and assists with study-related analysis. Mrs. Russell coordinates timely communication with the  office of Research Affairs, Research Protection Programs , Principal Investigators, clinical research staff, and project sponsors.  She ensures the quality management of regulatory documents by continuing review and submission of required documents in compliance with Federal, State, and local standards.

Mrs. Russell received a Bachelor of Science in Neuroscience from Brigham Young University and a Master of Arts in Bioethics from the Medical College of Wisconsin.  She has an extensive background in both clinical research and research ethics.

  

 

 

 

 

 

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Rebecca Mijal, BSAS Phone: (909) 651-5002
Regulatory Affairs Coordinator, CTC E-mail: rmijal@llu.edu

 Ms. Rebecca Mijal coordinates study regulatory submissions for grant funded research projects managed by the Clinical Trial Center.  She is responsible for supporting the PI and clinical research staff through timely communication, preparation and submission of all regulatory documentation and ensuring that documents are in compliance with Federal, State, and local laws.  Ms. Mijal also collaborates with Research Affairs, Research Protection Programs, Principal Investigators and clinical research staff to ensure accurate and timely submissions.

Ms. Mijal received a Bachelor of Science in Applied Science from the University of Wisconsin. She has three years of experience as a clinical research associate focusing on various therapeutic areas and has substantial knowledge of the clinical research process.

 

 

 

 

 

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Zeresh King, BSBA Phone: (909) 651-5002
Administrative Secretary, CTC E-mail: zking@llu.edu

Ms. Zeresh King provides administrative support to the CTC.  She works to facilitate the Clinical Trial process by communicating with investigators, coordinators, clinical trials personnel, and Research Affairs to schedule feasibility meetings and coordinate communication.  Zeresh provides secretarial, data, and clerical support to the CTC in order to facilitate the implementation and management of clinical trials.  She also collaborates with departments to coordinate ancillary support for clinical trials.  She maintains knowledge of institutional research resources and research department contacts and respond to inquiries with accurate and timely information.   

Ms. King has been employed with Loma Linda University for three years and has over thirteen years of experience as an Administrative Assistant.  She earned her Bachelor of Science in Business Administration from ITT Technical Institute.  She is currently completing her Masters in International Business with a consentration in Health Services at Keller School of Management.