Farhad Rahaman

Director, Clinical Laboratories @Immunovant

NY, US

1) Oversight of Central Laboratories, including:• Reviewer and signatory for regulated documents provided to laboratories to permit the collection, processing, shipment, and analysis of biological samples from clinical trial participants.• Protocol and amendment review for assessment of laboratory impact against program timelines.• Troubleshoot preanalytical, analytical, and postanalytical issues that impact sample analysis.• Participate and monitor third-party laboratory system version updates.• Foster partnerships with laboratories via standing meetings and on-site visits.• Designated business owner for study contracting. • Partner with data management to ensure appropriate laboratory details in compliance with data transfers. • Participate in the selection and onboarding of new vendors.• Provide laboratory timelines to key stakeholders.• Participate in site-activation/initiation meetings and/or visits.• Facilitate ongoing review of processes to provide continuous improvement recommendations. 2) Oversight of specialty laboratories that validate bioanalytical methods and perform sample analysis for pharmacokinetic, pharmacodynamic, anti-drug antibody, and non-routine biomarker studies.• Review validation and sample analysis plans.• Review and interpret validation data and ensure compliance with regulations.• Manage timelines and logistics for the delivery of biomarker data.• Ensure labs have available investigational product and critical reagents to support Immunovant studies.3) Work closely with Immunovant cross-functional project teams to provide technical input on laboratory procedures.• Participate in periodic Team meetings and provide laboratory updates.• Investigate isolated analytical/logistical issues that could impact participant enrollment.• Identify trends that may require Clinical Labs intervention to improve efficiencies.• Contribute to regulated clinical trial documents (e.g, study protocols).

C.R.T.I online-Certificate of Completion

CRA Professional Development :Clinical trial Monitoring & Research Site Coordination;ICH;GCP, Clinical Research

Iona University

Master of Business Administration (M.B.A.), Financial Management

Concordia University

Bachelor of Science (B.Sc.), Biology