Principal Responsibilities
- Contribute to the TA strategy through researching the medical environment identifying and building relationships with KEEs and through the planning preparation of advisory board meetings.
- Participate in program meetings to stay updated on the latest progress and provide expert opinions as needed to support team discussion and decision-making.
- Act as a point of contact for global clinical development expert
- Review and provide expert input on program related documents (e.g. protocol IB)
- Review and/or provide expert input on documents for regulatory interactions (e.g. briefing document for PMDA Orphan drug designation application)
- Review and provide expert input on relevant parts of filing documents (e.g. CTD J-PI RMP).
- Prepare responses to clinical part of PMDA inquiries in collaboration with JPTL and other JPT members.
- Contribute to discussion of PADG team in collaboration with JPTL and medical affairs.
- Review and expert input on publication strategy and contents/quality of publications.
- (In case of a Japan stand-alone study) create study documents (e.g. protocol concept sheet)
Qualifications
- Minimum of eight (8) years of experience in drug development in pharmaceuticals biopharmaceuticals or biotechnology.
- Experience in Phases 1 to 3 as a clinical scientist.
- (Preferred) Experience working in a global pharmaceutical company
- Extensive experience as a clinical scientist including KEEs engagement AdB meetings preparation of clinical documents (e.g. protocol IB) regulatory interactions filing preparation and post-filing inquiry resolution.
- Knowledge of local regulations and guidances
- English skills that enables communication with global team.
Education
- Life Science related bachelors degree
Others
- Business Trip Available; Visit to mainly domestic medical institutions/doctors domestic conferences etc.
Date Posted
0
Closing Date
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Required Experience:
Director