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NOVARTIS
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Medical Expert

Medical Expert

NOVARTIS

5 - 10 years

15 - 16 Lacs

Hyderabad

Posted:1 day ago| Platform:

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Skills Required

Internal medicine Scientific writing Hematology Pharma Clinical trials Clinical research Oncology Medical writing biomedical Drug safety

Work Mode

Work from Office

Job Type

Full Time

Job Description

Summary

The Medical Expert in TCO (Translational Clinical Oncology) is the medical leader for assigned global, roll-over and long-term follow-up studies, and studies in the close-out phase. They may also provide medical co-leadership for assigned aspects of one or more global, active, TCO study, under the leadership of a Clinical Program Leader (CPL)
TCO (Translational Clinical Oncology) is a department under Biomedical Research division, and is responsible for designing and executing out early phase (first in human) clinical studies in patients with cancer. It acts as a bridge between drug discovery and late phase clinical development and strives to deliver transformative new medicines for oncology conditions.

About the Role

Major accountabilities:

Provides medical support to Clinical Program Leader (CPL) leading the program. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables.
May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team.
May represents CPL at project team meetings (e.g. CTT) and may provide inputs to project strategy
May represent CPL at Investigator teleconferences including dose escalation meetings and site initiation visits.
Oversees the clinical/scientific elements of TCO related submission documents, including preparation and review of project documentation for Health Authority submission, including briefing books, IBs, Annual Safety Reports, responses to Health Authority questions etc.
Leads the ongoing clinical trial data medical/scientific review across assigned TCO studies and coordinates data analysis and interpretation
Accountable for assigned close-out, roll-over and long-term follow-up studies, ensuring Clinical Study Report review, consistency and quality of clinical study reports (CSR) in collaboration with CSR medical writing team, and publication of studies across assigned TCO projects - either directly as lead author or by providing leadership to the medical writing team
Manages stakeholder engagements internally and externally
Mentors and coaches junior TCO team members in India
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, 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.
Strong evidence of quality medical review of trial data and quality contributions to clinical sections of e.g. protocols, IBs, DSURs and CSRs
Contribution towards objectives set for the department.
Feedback from external and internal stakeholders.
Clearly demonstrates Novartis Values and Behaviors.

Minimum Requirements:

Education:

MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine / pharmacology etc.) with medical council certification required.
Experience in hematology / oncology preferred

Work Experience:

At least 5 years of pharmaceutical/biotech industry experience
At least 2 years of clinical practice experience in the hospital setting.
Experience with oncology clinical trials
Experience with early development clinical trials
Knowledge of Good Clinical Practice (GCP).
Strong operational project 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 key stakeholders, 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.

Skills:

Clinical Monitoring.
Clinical Research.
Clinical Trial Protocol.
Clinical Trials.
Decision Making Skills.
Drug Development.
Health Sciences.
Lifesciences.
Medical Strategy.
Regulatory Compliance.

Languages :

English.

Benefits and Rewards:

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Medical Expert