Provide thorough up-to-date medical, clinical development and relevant commercial expertise to drive Novartis message delivery to key influencers and stakeholders.
Collaborate with CPO, Regional and Global team members in the execution of relevantclinical activities in assigned project(s).
Expertise and Medical support : Contribute medical, clinical expertise and scientific advice to all allied departments in local CPO including support to the local ICRO team for timely execution of studies conducted in the CPO and to DRA in interactions with authorities.
Collaboration : Collaborate effectively with CPO, Regional and Global Teams in the execution of relevant clinical activities, including initial input in protocols and ongoing medical support.
Global teams : May serve as CPO representative on Global Teams, as assigned. Strategy : Drive the C4MPH strategy and contribute to strategic alignment of assigned Development Project(s) and Brand(s) in local BF / BU.
Local studies and publication : Plan, initiate, manage the implementation and drive timely publication of Post Phase III clinicalactivities including local profiling programs when applicable.
Safety : Responsible for local clinical trial oversight of adverse event reporting together with CS&E as well as clinical input into adherence to GCP, and in line with ICH and local regulations.
Investigators : In collaboration with Clinical Operations (ICRO), advise / recommend potential investigators for local and global studies, ensuring the right mix of KOLs.
Medical Affairs / Mktg : May function as the medical product champion. Work as strategic partner with Marketing for Nov Dev project(s) and marketed product(s).
Customers : Meet customers needs and expectations with regards to assigned Brand(s) for delivery of Nov messages to key influencers and stakeholders as the brand champion interface for internal and external customers.
SciOps : Work with Scientific Operations / Medical Scientific Liaisons proactively to ensure market preparation pre- and post-
launch. NP4 / Materials : May create, review, and approve promotional and training material tailored to the needs of the product and according to NP4 and local regulations.
KOLs : Supports SciOps and MICS for proactive data dissemination to reinforce clinical awareness, and develop and maintain the support of KOLs, influencers and key external stakeholders.
Training : Provide comprehensive product / disease and therapies presentations and training to internal and external customers, including the field force, for the accurate delivery of messages in line with global plans.
Image : Maintain ethical standards of CPO operations to contribute proactively to a credible image for CPO in the local Health Care and Medical community.
Management : May lead local clinical
Medical / Veterinary Degree, as per CPO strategy and / or local regulations. Fluent in English (oral and written) CPO country language preferable 1.
Typically would have more than 2 years experience in clinical medicine and / or research 2. Good planning skills. 3. Medical and scientific writing skills.
4. Knowledge of assigned therapeutic area with ability to interact with relevant KOLs. 5. Familiar with all aspects of drug development, GCP and local regulations, including regulations of Promotional materials.
6. Knowledge of clinical trial design statistics and pharmacokinetics. 7. Familiar with marketing principles and strategies.