Senior Manager, Clinical Scientist at IQVIA leading clinical activities and collaborating with stakeholders. Manage timelines, draft documents, and ensure high-quality deliverables for clinical research.
Responsibilities
Lead and coordinate various clinical activities
Collaborate with physicians and stakeholders
Manage timelines and clinical synopsis process
Create study design and ensure internal team review
Generate initial drafts and manage review processes
Lead discussions and summarize findings with stakeholders
Ensure accuracy of documentation and consistency across submissions
Requirements
Life Science PhD or MD (or equivalent)
Minimum 5 years of relevant clinical research or related industry experience
2 years and above experience in drafting clinical study synopsis and clinical sections of key regulatory documents (Must have)
Experience in a drug development or pharmaceutical environment
Familiarity with regulatory and sponsor interactions
Demonstrated ability to design and implement complex clinical protocols.
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