Medical Value Partner

Indonesia, Giacarta, Jakarta

en de fr es ru tr pt zh ja

You will be responsible for :

Medical Plan & Therapeutic Area Expertise

  • Development and execution of medical activities related to the strategy within the Integrated Therapeutic Area (TA) plan.
  • Subject matter expert for the Therapeutic Areas and focus on pipeline shifts, PHC/ RWD, Digital.
  • Understand the current and future (competitive) landscape and healthcare system to identify any (medical) gaps and proactively create solutions.
  • Maintain regular contacts with local investigators for key studies
  • Planning and execution of relevant Medical advisory boards and expert meetings
  • Ensure compliance of contractual engagement of HCPs including review and approval of agreements/grants.

Execution Excellence:

  • Focus on Value based communication: Manage the integrity and accuracy of scientific data communicated both internally and externally for promotional and non-promotional
  • Redefines partnership by working closely with external stakeholders (HCPs,
  • Reimbursement and Policy makers, Patient Advocacy Groups etc.)
  • Ensure optimal mix of medical activities (insight gathering, internal and external knowledge exchange, training, evidence generation) to realize early access to our treatment solutions.
  • Act as Medical Information (MI) Responsible (refer to MI Responsible JD)

Data Generation

  • Identify local data gaps, local studies protocol design, study planning (including budget), input to site selection and feasibility assessment, data dissemination strategy.

Training & Coaching

  • Collaborate with Marketing Partner in training and inducting sales team to ensure the high quality knowledge of Brand and therapy areas

You will demonstrate the following qualifications:

  • Medical doctor* by education from a registered university
  • Professional experience of pharmaceutical industry
  • desirable.
  • Understand the local healthcare system, business (reimbursement and policies) and relevant laws and regulations.
  • Knowledge of drug development process, Clinical trial (ICH/GCP), Good Pharmacovigilance Practice (GVP), Early access programs and Statistics.
  • Experience in the principles and techniques of data analysis, interpretation, clinical value proposition and delivery of scientific presentations
  • Experience in developing good collaboration with external stakeholders and co-creating solutions for patients.
  • Experience in resolving complex issues in matrix organization.
  • Fluent in written and spoken English
  • Agile Methods adoption
  • Digital engagement