Wendy Wright

Clinical Project Associate Director @IQVIA

Chelmsford, GB
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Mar 2024 — Present

Clinical Project Associate Director @IQVIA

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EDUCATION

1986 — 1990

University of Surrey

Biochemistry (Medical) BSc, Biochemistry

SKILLS

Clinical MonitoringOncologyPhase IPhase IiClinical Research AssociatesIch-GcpLeukemiaLine ManagementInformed ConsentPhase IiiClinical Data ManagementHaematology OncologyIrasClinical TrialsEdcTherapeutic AreasClinical ResearchCtmsMentoringProstate CancerRegulatory SubmissionsBid PreparationRegulatory DocumentationInformCRORbmGcpClient Facing SkillsClinical DevelopmentPresentation SkillsThird Party VendorsDirect SalesDermatology

ABOUT WENDY WRIGHT

A Clinical Project Associate Director with extensive experience handling all phases of/Phase I,II, and IV clinical trials in Pharmaceutical, Biotech and CRO environments, I have been involved in clinical research since for over 20 years and have worked in a broad range of therapeutic areas. During this time I have managed the full scope of activities as Project Manager, overseeing all functional areas with vendor management, and serving as a primary contact with the sponsor and ensuring that deliverables are provided on time and within budget. My previous experience also includes clinical study management covering activities such as Investigator and site selection, training and mentoring staff, identifying and resolving study site issues, assisting in writing and updating SOPs and overseeing vendors. My knowledge of regulatory inspections has meant that I have successfully supported projects through FDA, MHRA and sponsor audits.Recent studies include specialising in Rare Disease, and Gene Therapy/Paediatrics. Therapeutic experience includes: Oncology ( Solid Tumour, Prostate, Hematologic, and Renal cancer), Dermatology, Emergency Medicine, Hematology, Gynecology, Infectious Diseases, and Gastroenterology.

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Wendy Wright — Clinical Project Associate Director at IQVIA in Chelmsford, GB | Unifers