Mohammad Mahbubur Rahman

Experience

• 

  Novo Nordisk

  Mar 2010 - Feb 2011

  Manager, Medical and Marketing

  • Act in line with ethical standards, company procedures and Way of Management which includes Vision, Policies and Charter which describes Values, Commitments and Fundamentals of the organization.• Ensure optimizing Medical Governance in all activities• Key resource personnel for medical information concerning products and therapeutic interest areas.• Accountable for pharmacovigilance and ensuring any AE passed to the International Product Safety Department. • Ensure that the profile of the organization remains high among stakeholders like doctors, patients, paramedics, associations, etc. by developing and maintaining a close rapport through liaison and networking.• Ensure a close and positive interaction between Medical and Marketing to build sharpen promotional strategies and their implementation.• Accelerate marketing efforts by organizing meetings, conferences, updates, CMEs and publications.• Organize education program based on basic medical knowledge on diabetes control and prevention of its complication for nurses, paramedics and patients in collaboration with government and non-government organization.• Develop, implement and review quality systems and implementation of quality policies within the department.• Educate and train field and marketing personnel regarding all aspects of disease, product and therapy relevant to the promotional strategy.• Responsible for conducting national and multinational study including verifying that the approval of the protocol and all GCP procedures as per the ICH-GCP guideline is followed. Show less

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  GSK

  Jul 2013 - Mar 2019

  Accountable for the governance oversight and implementation of Scientific Engagement principles and operating practices• To secure clinical Research and Development for Bangladesh by ongoing interactions with central GSK research divisions, regulatory authorities, key opinion leaders and investigators to ensure continued involvement in clinical trials.• To negotiate and manage clinical trial legal agreements and budgets between the investigators and GSK• To conduct clinical trials in accordance with ICH, GCP and local Ethics Committees and legislation.• To provide medical support to the marketing division to ensure successful commercialisation of products throughout their life cycles.• To review and approve promotional materials to agreed SOP taking into account latest codes of conduct.• To provide a robust Medical Information Service to both internal and external customers. • To ensure training including Adverse Events and Promotional Code is conducted at induction for all new GSK staff• To maintain a drug safety reporting system in accordance with GSK and legislative requirements as Person Responsible for Pharmacovigilance (PRP) for Bangladesh• As PRP for Bangladesh, have overall accountability for pharmacovigilance, materiovigilance and human safety related activities for all marketed products and products in clinical trials, including all Pharma products, vaccines and for Consumer Healthcare products as per the share service agreement between Consumer Healthcare and Pharma.• To ensure ongoing self-development and training in order to maintain excellent personal performance necessary to maintain GSK’s image as a leader in research and development.• Support implementation of QMS compliant process for medical function for the relevant identified activities as per Target Operating Model Show less

  • Area Medical Operation Director

    Aug 2017 - Mar 2019

  • Director, Clinical R&D and Medical Affairs

    Apr 2014 - Mar 2019

  • Head, Clinical R&D and Medical Affairs

    Jul 2013 - Apr 2014
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  Novo Nordisk

  Mar 2019 - Jul 2021

  • Director, Clinical, Medical, Regulatory & Quality

    Oct 2020 - Jul 2021

  • Head of Clinical, Medical, Regulatory and Quality

    Mar 2019 - Oct 2020
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  Novartis

  Jul 2021 - now

  Chief Scientific Officer