Michael Stephens

Sr Dir, Clinical Operations - Global Site Management @Immunovant

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

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WORK HISTORY

Jun 2024 — Present

Sr Dir, Clinical Operations - Global Site Management @Immunovant

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Manchester, GB

Part of the Global Site Management LT responsible for driving clinical site oversight and relationship management ex-US. The role also partners with Clinical Operations/Clinical Development/Medical Affairs/CRO to define strategy for study country footprint and site selection.

EDUCATION

1984 — 1988

Cardiff University / Prifysgol Caerdydd

BS, Clinical Immunology, Toxicolgy & Biochemistry

1988 — 1992

University of Cambridge

PhD (Cantab), Clinical Immunology of HIV infection

SKILLS

Vendor ManagementRegulatory SubmissionsClinical MonitoringDrug DevelopmentClinical DevelopmentCross-Functional Team LeadershipVaccinesFdaClinical TrialsSop21 Cfr Part 11Therapeutic AreasRegulatory AffairsGood Clinical Practice (Gcp)Medical AffairsBiotechnologyVirologyLifesciencesEdcMedical WritingPerformance ManagementClinical OperationsBiopharmaceuticalsClinical Data ManagementElectronic Data Capture (Edc)Standard Operating Procedure (Sop)EndocrinologyImmunologyU.s. Food and Drug Administration (Fda)PharmacovigilanceGastroenterologyCtmsTeam ManagementTeam BuildingClinical ResearchInfectious DiseasesCRORheumatologyHematologyChange Management

ABOUT MICHAEL STEPHENS

More than 25 years dynamic management experience of effectively leading clinical research operations projects, teams & people in UK, US, EU, & Australia- Successful experience of formal meetings with Regulatory Agencies (EMA, FDA, MHRA, PEI, AEMPs and others)- I have delivered both strategic & tactical operational roles within Remote home office, Corporate, Regional or Affiliate settings, including WFH in a full home office set-up for the past 9 years- Achieved positive results in clinical research through effective vendor management, to meet recruitment targets, reporting timelines, and budget limitations whilst maintaining a state of Inspection Readiness- Leadership of Clinical Field Operations teams in the execution of clinical trials using in-house, out-sourced, and hybrid clinical teams, including use of an FSP for US site management and monitoring, and the use of SMOs- I have driven significant change management process initiatives to enhance departmental effectiveness, efficiency & quality- Experience of working in collaboration with Regulatory Affairs colleagues with both the EMA & FDA on the clinical component of BLA/MAA/NDA filings. Goal: To be the best that I can be. Specialties: Clinical Research deliverables to time, quality & budget. Team building & performance management. Organization building and change management. Resource allocation, clinical trial budget forecasting and management. Regulatory inspection readiness and Agency GCP Inspections. CRO/Sponsor relationship management. Clinical site relationship management. Vendor management of IVRS, central laboratories & EDC. On a personal note, my main interests reflect my team player mentality in that they are mainly of a sporting nature. Football, rugby union, cricket and gym training are my favourites, whenever time permits. I am a season ticket holder at my beloved Old Trafford. I also enjoy travel, films, and cooking.

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Michael Stephens — Sr Dir, Clinical Operations - Global Site Management at Immunovant in Manchester, GB | Unifers