Main tasks

✓ Under the oversight of the Medical Director as well as Evidence Generation Leads, you contribute:

• in setting-up of global medical peri-launch activities on glioma
• to the development of MSL & Local Medical Leads training materials on Vorasidenib
• to coordinate global/local/network animation to address country medical strategy needs
• to review and develop medical scientific publications & information in relation with the therapeutic domain

✓ Under the oversight of the Evidence Generation Lead, autonomous & proactive contribution of the programs, from conception to realization:

• Engagement with experts and support of the RWE Steering Committee
• Analysis and interpretation the results of the study, validation of study reports
• Contribution to internal and external communication of study results (Abstracts, publications, posters…),
• Design of clinical studies (phase IIIb and IV) and other evidence-generation programs: rationale, synopsis, protocols, technical documents…
• For IIT Program management: provide critical input on proposed third party concepts from investigator-initiated trials and collaborations
• Sub-contracting: support drafting of the specifications & definition of deliverables, follow-up of subcontracted activities with institutions and hospitals taking part in investigators sponsor studies & RWE collaborations

✓ Work in close collaboration:

• with the key medical affairs stakeholders: evidence generation lead, medical communication lead, publication manager, local medical leads and MSLs
• With other departments and be their main contact for the activities you coordinate: R&D, global marketing and market access, affiliates
• With external partners: experts, cooperative groups, investigators, vendors (CROs, agencies…)

✓ Good practices:

• Regarding medico-scientific, operational and legal
• In compliance with internal procedures (SOP), applicable regulation (GCP, GVP) and compliance rules (Fair Market Value).

Your strengths

• Strong interest for medical & scientific understanding, clinical & medical practice
• Previous experience in clinical studies management is a plus (Phase 3b, Real World Evidence, early access patient programs, Investigator-Initiated Trial programs)
• Oncology therapeutic area knowledge is optional, but willingness to learn and adaptation capability is needed.
• Ability to work globally and cross functionally, and to contribute to multiple projects with an analytical vision & strong synthesis capabilities
• Excellent communication skills in working with cross-functional and multi-cultural teams (oral and written English)
• Positive and committed attitude, solution and results driven, collaborative mindset

Your background

PhD student in Medicine or Pharmacy - complementary business school curriculum is a plus

Your experience with us

• Join an experienced, dynamic and multicultural team with diverse backgrounds !
• Duration : 6 months
• Contract : internship
• Location : Suresnes & remote work

Description du profil :

Profil recherché

• Medicine or Pharmacy student or life sciences, such as biology, biochemistry, or business school with life science

Vos points forts

• Strong interest for medical & scientific understanding, clinical & medical practice
• Previous experience in clinical studies management is a plus (Phase 3b, Real World Evidence, early access patient programs, IIT Program)
• Oncology therapeutic area knowledge is optional, but willingness to learn and adaptation capability is needed.
• Ability to work globally and cross functionally, and to contribute to multiple projects with strategic, analytical vision and business understanding
• Excellent communication skills in working with cross-functional and multi-cultural teams (oral and written English)
• Positive and committed attitude, solution and results driven, collaborative mindset

Notre proposition 

• Intégration à une équipe expérimentée et hyper dynamique
• Durée du stage : 6 mois/12 mois
• Type de contrat : stage/alternance
• Lieu : Suresnes et télétravail