Lowongan Novartis (Dibuka : 27 Juni 2012)


Informasi Detail Lowongan

Medical Science Liaison
Perusahaan
Novartis
Lokasi
Jakarta, Jakarta
Dibuka: 27 Juni 2012 - 11 bulan yang lalu


Kirim Lamaran

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Novartis memberikan persyaratan, ketentuan dan spesifikasi pekerjaan sebagai Medical Science Liaison yang akan ditempatkan di Jakarta, Jakarta.

Dibawah ini rincian lengkap persyaratan, spesifikasi lowongan pekerjaan, jadual wawancara dan alamat serta kontak (email / nomor telepon) perusahaan Novartis. Untuk mengirimkan lamaran, klik pada tombol 'Kirim Lamaran Sekarang' dibawah.

Spesifikasi dan Persyaratan Pelamar Pekerjaan Novartis

Build scientific partnerships with healthcare professionals and decision makers to build advocacy. Strategically prepare and support the development, launch and commercialization of drug products through education of KOLs/Key Stakeholders, education of the scientific community and KOLs, clinical trial support, and by the scientific exchange seeking external insight to shape Novartis commercial and development programs.

KOL Management & Medical Support 1. Contributes to mapping / profiling of KOL/decision makers in line with segmentation 2. Develop professional relationships, build advocacy and gain contributions of KOL/decision makers. 3. Collect, analyze and report insights that may impact Novartis development plans /trial designs. 4. Provide and discuss scientific information and data to healthcare professionals to ensure quality and accuracy of medical and scientific information on new treatment options including Novartis products and selected areas of therapeutic interest. 5. Liaise and provide up-to-date medical support to relevant external groups to facilitate listing of products in medical guidelines, formularies to impact pricing and health-economic discussions. 6. Provide speaker training to health care professionals to support the best use of new therapies developed and commercialized by Novartis.

Clinical Development Support 7. Contribute to the identification of appropriate clinical investigators and facilitates placement into Novartis sponsored clinical trials. 8. Support the investigational sites, as needed , as part of a cross-functional team with ICRO and the Medical Advisor and others as appropriate. 9. Identify clinical investigators with research proposals that are consistent with our product development strategies and facilitate the Investigator-Initiated Research Protocol (IIRP) process including study completion, presentation, and publication, as appropriate. 10. Support the investigators to comply with the IIRP process in accordance with the guidelines and NIPs, providing knowledge and guidance for legal and financial local regulations, as appropriate.

Information Management/Insights 11. Collaborate with Novartis colleagues to actively support medical and scientific meetings by collecting and interpreting insights /presentations/ results. 12. Evaluate the impact of competitive information to share internally and externally as post-meeting deliverables.

Internal Novartis Support 13. Provide medical support and training (i.e. disease state and product) to Novartis colleagues (e.g. sales reps, CRAs, etc.). 14. Screen business opportunities. 15. Serve as a resource for projects and collaborate with internal colleagues. 16. Collaborate with Medical Advisors/TA Medical Teams and other cross-functional groups (i.e. Marketing Teams, KAM). Minimum requirements Required: be considered as a peer of the customer base. MD, pharmacist, with solid medical/technical back-ground and proven competencies influencing skills, clinical research insight, business and market know-ledge.

Fluent in English & Local Language (oral and written).

1. Proven ability to develop and foster peer-to-peer, credible relationships in order to educate and negotiate KOL/decision makers. 2. Working knowledge of the Healthcare System and of the research procedures as well as the ICH guidelines, GCP and other ethical guidelines relevant to the pharmaceutical industry, 3. Thorough knowledge of clinical medicine, disease management, and medical research in at least one therapeutic area. 4. Ability to synthesize recent scientific information, analyze them within strategic and regulatory settings. 5. Strong personal integrity, and customer focus. 6. Excellent interpersonal communication, negotiation and advanced presentation skills. 7. Effectively contribute to work on multifunctional teams. 8. Must be able to adapt, organize, prioritize, and work effectively in a constantly changing field-based environment.
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