Drew Haigh Email & Phone Number

North Wales, PA, US

Plymouth Meeting, PA, US

• Managed creation of patient narratives, focusing on demographics and outcomes to prioritize patient experiences throughout the trial
• Analyzed data and created easy-to-follow Excel sheets and graphs that consolidated data to support senior management decision-making
• Worked closely with clinical site staff and investigators to obtain accurate study data, ensure protocol compliance, and guarantee patient safety through general correspondence and utilization of Clinical Trial.
• Assisted with the creation and review of various essential study documents, including: RGAs, SRFs, staff training forms, protocols, ICFs, and IBs
• Created and managed thorough enrollment projection tracker, overseeing patient visits throughout trials and ensuring patient enrollment needs were met
• Collected regulatory documentation and maintained TMF/eTMF to ensure compliance with GCP, ICH, regulatory authorities and ethics board requirements

Ashby-de-la-Zouch, Leicestershire, GB

Interact with patients suffering from chronic diseases: Crohn’s disease or ulcerative colitis, forms of inflammatory bowel diseaseCollect and accurately document confidential, medical information from callers, such as: healthcare professionals, patients, or caregiversRecognize and report adverse events experienced by patients while using the program’s.

Plymouth Meeting, PA, US

Took part in the startup and closeout of new infectious disease vaccine clinical trials Participated in the development of templates and protocols to ensure that the program met regulatory and legal guidelines Scheduled meetings with various professionals and research groups and write up accurate meeting minutes to keep track of exchanged information.