Novartis D Pharma Global Program Safety Lead Post Vacancy

Novartis D Pharma Global Program Safety Lead Post Vacancy

Novartis hiring D Pharma candidates for the post of global program safety lead. Pharma job opening 2021. D Pharmacy job 2021. Novartis hiring safety lead. Interested and eligible candidates may apply for the job vacancy and check out all the details for the same below:

Job Title: Global Program Safety Lead

Job Id: 326672BR

Minimum requirements

• Medical Degree or equivalent (preferred), Ph.D., PharmD or equivalent graduate-level health care professional degree required. Specialty Board certification desirable.

• Postgraduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent)

• 3 years clinical experience postdoctoral; At least 5 years are in drug development in a major pharmaceutical company (of which 2 years in a global position), including 2 years in safety at an operational or medical position

• Experience in preparing or contributing to the preparation of clinical safety assessments and regulatory re- ports/submissions involving safety information

• Experience in leading cross-functional, multi-cultural teams; Experience with (safety or others) issue management

• Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics, and writing of publications

Job Description

Your responsibilities include, but are not limited to:

• Provides

expert safety input to the clinical development program for assigned projects/products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Is responsible for safety issue management from the formation of Global Program Team (GPT) through Life Cycle Management.

• Develops and is responsible for key internal Novartis safety documents: reviews these documents regularly and updates as required (e.g. when significant new information is received). Ensures that these, and all other project-related safety documents, are consistent in safety messages.

• Owns the safety strategy and document it in the corresponding documents (e.g. dSPP, SSPT) and leads the production of the medical safety deliverables (e.g. DSUR, PSUR, RMP) for the assigned products.

• Is responsible for overall signal detection, monitoring, evaluation, interpretation, and appropriate management of safety information, based on information from all relevant line functions, post-marketing data, and other sources. To this end, constitutes and runs the Safety Management Team (SMT). Ensures that this team appropriately and timely reviews all medical safety data from various sources (e.g. pre-clinical, clinical trial data post-marketing, literature) throughout the development and post-approval process.

• Responsible for documentation/tracking/record keeping of the assigned compounds’ medical safety activities. Is responsible for initial development and ongoing maintenance of safety information in Core Data Sheet (core global labeling), including addressing safety issues optimally in all project/product labeling indications.

• Is responsible for responses to inquiries from regulatory authorities or health care professionals on safety issues. Leads the preparation of the safety strategy for health authority responses and strategy, in collaboration with other project team members.

• Prepares safety data for health authority review boards (together with the clinical and biostatistical functions). Attends Health Authority Meetings in person, as required. Is responsible for responses to legal queries and Country Organization (CO) requests involving safety issues. Provides integrated safety input into all regulatory documents required during active development.

• Ensures safety information is communicated/escalated to HPS/MPH, HMS HYD, and/or EU Qualified Person in a timely fashion. Facilitates involvement of external experts (e.g. authors of white papers, members of trial-specific data safety monitoring boards, ad-hoc support for HA meetings, etc.).

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