...needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing develo...
...the impact you could have.
Job Purpose:
The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing... ...and diverse teams representative of the patien...
...The Clinical Project Leader (CPL) / Local Study Manager (LSM) is part of the Clinical Study Unit (CSU), and is accountable for the strategic... ...area in terms of study management and conduc...
...Provide scientific expertise, build knowledge and activity based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer s image in the s...
...documents we authored last year. As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory s...
...improve health outcomes that people and communities depend on – now and in the future.
Division Specific Information
As a Senior Medical Writer, you will serve as the primary author by writing and providing in...
...affairs colleagues to support them in implementing the medical activities relevant to the brand plan strategies for specific products and therapy areas as appropriate.
Develop and customize presentations when req...
...As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinica...
About the Role
Position Title: Expert Regulatory Writer
About the role: Expert Regulatory Writer
Location – Hyderabad #LI Hybrid... ...Reports (CSR), Risk Management Plans (RMP), Complex Comm...
