Carly Hadman

WORK HISTORY

EDUCATION

SKILLS

ABOUT CARLY HADMAN

I have worked in the pharmaceutical industry for over 20 years, specialising in Data Management, Pharmacovigilance and Business Analysis. My experience includes- over 14 years experience as a Lead Clinical Data Manager, with CDISC/SDTM expertise, providing oversight management of DM CROs and vendors. Experienced in rare disease, immunology, infectious disease neurology and oncology clinical trials- Lead DM for complex trials, including food effect, dose escalation, multiple arm oncology trials, with data types such as imaging, PK, biomarkers, ePRO, dosimetry and actigraphy- 6 years experience in Clinical Systems, including the implementation and training of new pharmacovigilance databases (EDC) and software, functional specification review, test creation, UAT (including for ETL and E2B), validation, documentation and end user training- 4 years experience in using BusinessObjects, including report creation, review and UAT - Systems Analyst/ SAS Programming experience for clinical trial data- encoding and validation programming- Excellent IT skills including Office, database administration and systems maintenance, BusinessObjects, SAS and Information Management- BSc (Hons) Medical BiochemistrySpecialities: Business Analysis, Clinical Data Management, CDISC, SDTM, CDASH, vendor management, study oversight, Drug Safety/Pharmacovigilance systems, EDC, GCP, User Acceptance Testing, FS review and test script creation, Business Objects Report Developer, Strong excel skills (macros, pivots, VLOOKUPs etc), systems maintenance, MedDRA and SMQs, SAS and SQL. Project management and Prince2 Practitioner.