Job Description Facilitate /drive drug development for responsible TA/ TAs and develop the scientific part of the brand strategy in alignment with the brand team and the global strategy. Has the overall responsibility to implement the scientific activities in the responsible therapeutic area/s in compliance with applicable policies, procedures and other regulations.
Drug Development/Clinical Research Support: Provide strong scientific input on the global CDPs being the medical expert in the CPO Provide medical expertise/advise for the ICRO/GMO teams: - Lead and/or perform protocol, country and site feasibility. - Provide protocol, Risk management plan & disease training as appropriate at Investigator’s Meetings or scientific forums or internally. - Review and try to resolve local medical issues / questions that arise during the entire course of the trial – if necessary transferring issues to global teams. - Support the regional/global teams on the local level. Develop, review and approve local studies’ documents.
Minimum Requirements MD, pharmacist, and other life sciences with solid medical/technical background and proven competencies, business and market knowledge.