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Clinical Scientific Experts Director

Secunderabad, Telangana
Job Code:
  • Biotechnology & Science
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Job Details

Lead and motivate the CSE organization, put appropriate structure in place Hire, build, develop and retain CSE Team including Clinical Scientific Experts and CSE Group Heads to support Global Drug Development clinical projects Deliver CSE contribution to key milestones for clinical Build an organization that owns clinical data review excellence. Lead and drive key strategic projects sponsored by Global Head of Clinical Development Ensure CSE resource planning is in line with Global Drug Development strategy Ensure Quality and Compliance goals are met aligned with local and global policies Provide strong support to the Clinical Development Medical Director day-to-day management of issues as well as preparation of periodic updates to CDLT/GDLT and other internal/ external stakeholders. Support all key milestones for clinical projects Hiring and retention to agreed targets CSE resourcing plan Quality and Compliance Performance management and Career development of CSE team Organizational development activities within the CD line function Role-model Novartis/CD culture Resourcing and delivery of key clinical projects Budgets including travel budgets at agreed to targets. Collaboration and effective partnerships with CDLT, Development Franchise Heads, TA heads, FHGPMs, and other line functions like GCTL, DM, QA Effective, open and inclusive communication Diverse, highly-motivated team in placeMinimum requirements Advanced degree in life sciences/healthcare (or clinically relevant degree) is required. Masters or PharmD. PhD or MD strongly preferred. Fluency in English (spoken & written) 5 years technical and operational experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organization or Academia 7 years experience in team/ matrix management Strong understanding of Global Drug Development processes, objectives and strategy across various disciplines /functions (e.g., development, commercial, providers, payers). Strong scientific background in basic and clinical research with good understanding and knowledge on drug development. Background in Strategic Planning / consultancy an advantage. Strong skills in leading and managing cross-functional projects with significant (visible) business impact. Significant experience, and proven ability to effectively engage & manage associates from widely varying backgrounds & functions within a dispersed and highly matrixed organization. Ability to work and gain trust at all levels of the organization. Ability to influence Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons
Degree: M.Pharm. (Pharmacy) | MD/ MS (Medicine) | Ph.D. (Doctorate)

Additional Degree: B.Sc. (Science)

Experience: 7-12


Clinical Research | Regulatory Affairs
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