Tco Physician Job in Novartis

Tco Physician

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Job Summary

About the Role

Major accountabilities:

  • Provides scientific and medical expertise on assigned clinical projects
  • Contributes to clinical strategy for the Asian region
  • Accountable for all aspects related to wind down projects including review of clinical data, and oversight of all CSR related activities
  • Contributes to clinical trial data medical/scientific review for assigned TCO projects and coordinates data analysis and interpretation including the development of first interpretable results, clinical study report, publications, and internal/external presentations.
  • Builds and maintains high performance cross functional teams in TCO and with partners
  • Manages stakeholder engagements internally and externally
  • Mentors and coaches junior TCO team members
  • Maintains expert knowledge of ICH-GCP, external regulations and procedures, and supplements by training and practice of Novartis SOPs and internal policies. Leads or assists with relevant trainings across TCO India
  • Advocate continuous improvement of quality
  • Ensure all activities of associates comply with company standards and local regulations

Key performance indicators:

  • Management of assigned studies to ensure execution according to timelines, budget and with high quality, ensuring adherence to international and local regulations.
  • Demonstrates excellent scientific writing skills to enable the development of quality trial reporting, and regulatory documents.
  • Effective risk management in design of synopses, operational planning, and clinical execution.
  • Contribution towards objectives set for the department.
  • Feedback from external and internal customers.
  • Adherence to Novartis Values and Behaviors.

Minimum Requirements:

MD required. Board certification or prior industry experience in oncology required.

Experience from early clinical development preferred


Work Experience:

  • >5 years of pharmaceutical/biotech industry experience
  • Experience with oncology trials
  • Experience with early development trials
  • Knowledge of Good Clinical Practice (GCP).
  • Strong operational project and management experience including excellent planning, prioritization, problem solving and organizational skills. Used to managing multiple priorities.
  • Demonstrated operational excellence and scientific contribution to both clinical and preclinical projects.
  • Strategic thinking: ability to network with and influence opinion leaders, clear and logical presentation of complex strategic issues.
  • Clear written and verbal expression of ideas, an active/proactive communicator.
  • Well-developed interpersonal skills, with a proven record of accomplishment of successfully interacting with, influencing and building strong positive relationships.
  • Used to working independently and in a team, being flexible and adapting in a changing environment.

Languages :

  • Fluent oral and written English
Experience Required :

Minimum 5 Years

Vacancy :

2 - 4 Hires

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