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Premium Employer

Sandoz

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4.0

based on 413 Reviews

388 Sandoz Jobs

TCO Physician

Sandoz

4.0

based on 413 Reviews

1-4 years

Hyderabad / Secunderabad

1 vacancy

TCO Physician

Sandoz

posted 2mon ago

Job Role Insights

Flexible timing

Key skills for the job

Pharmacy Data Analysis Clinical Data Management Risk Management GCP CCTV Monitoring

+ 3 more

Job Description

Medical expert for TCO (Translational Clinical Oncology) trials. Provides global medical leadership for TCO wind down studies and global co-leadership for active TCO studies when appropriate.

Job Description

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.