Mandy Williams Email & Phone Number

Irvine, California, US

Irvine, California, US

Member of a small clinical operations team supporting CDI trials. Duties include but not limited to oversight of vendor activities associated with selection, activation, oversight and closure for PRISM4 study. Responsible for consent form approvals associated with both central and local ethics boards. Collaborate across functional teams to write and revise.

Member of a small clinical operations team, responsible for study start up deliverables for assigned studies that are of moderate to high complexity. Partner with the Clinical Project Manager, Clinical Site Liaison, Site Operations, CRO representatives, investigative sites and other vendors as required to perform study activities. Primary focus was study.

New York, New York, US

Serve as the primary point of Pfizer contact for investigative sites. Relationship duties included but not limited to accountability for site start-up activities through site activation; accountable for building and retaining investigator site relationships and providing support from site recommendations through the life cycle of studies. Activities.

Fort Washington, PA, US

Embedded position within Pfizer to oversee country and regional level activities for Pfizer studies. Responsible for recruitment and retention of investigative sites. Duties included but not limited to site qualification and feasibility reviews, trial recommendations and confirmation, and study start up activities. Serve as liaison between CRO and sites in.

Fort Washington, PA, US

Contracted to industry sponsors to complete study monitoring duties for investigative sites participating in clinical research studies to ensure adherence to ICH-GCP and protocol compliance. Duties included but not limited to sponsor and site communication, issue identification, reporting and resolution, query review and oversight, participation in.

Fort Washington, PA, US

Perform duties as a remote based clinical research associate for pharmaceutical research trials. Oversee SDV and compliance at site level both remotely and at investigative sites. Communicate trial progress, issues/actions related to protocol adherence and compliance and oversee retraining/resolutions as needed.

Oklahoma City, Oklahoma, US

Clinical Research Specialist with Integris Baptist Medical Center Nazhi Zuhdi Transplant Institute.

Research mineral title interest for the development of leasing in the petroleum industry. Create ownership reports based on specified mineral tracts. Transcription of ownership records from Land Patent to present.Includes mineral owners, leasehold owners, working interest, working interest held by production (HBP) and other projects as contracted.

Assist physician with conduction of clinical research studies (Phase IIa-IV). Ensure compliance with regulatory agencies, ethics board regulations, IATA, FDA and OHRP Good Clinical Practice Guidelines, International ICH Guidelines, and local regulations. Responsibilities include by not limited to: regulatory documentation compliance, patient management.

Assist physician in implementing pharmaceutical industry sponsored clinical research studies (Phase II-Phase IV). Ensure compliance with state, ethics and federal regulatory agencies, IATA compliance, as well as ensure all procedures are conducted within the guidelines of OHRP and FDA Good Clinical Practice Guidelines. Responsible for organizing and.

Responsible for management of all aspects of site level clinical trial administration at an SMO. Duties included but not limited to regulatory document completion; study selection and feasibility; investigator recruitment and retention for the SMO; subject recruitment and retention; coordinating communications between subjects, investigators and sponsors.