Senior Medical Content Specialist for Global Biosimilars
23 hours ago
At Biocon Biologics, we are creating a model for the future of healthcare that prioritizes patient-centricity and affordable innovation. We are a leading company in the biosimilars revolution, where patients come first.
The ideal candidate will be responsible for developing and managing scientific documents that support our strategic objectives. This role requires a strong understanding of clinical research, regulatory requirements, and the ability to communicate complex scientific information clearly and effectively.
Responsibilities:
- Planning, organizing, tracking, and archiving clinical and post-marketing regulatory dossiers.
- Managing stakeholders across line functions and geographies.
- Developing cross-functional skills in publication writing.
- Collaborating with the clinical team in developing and strategizing the Clinical Development Plan.
- Interpreting, representing and summarizing clinical and scientific data
- Managing assigned individual projects and holding complete responsibility throughout the document/project lifecycle.
- Ensuring consistency at all times with compulsory and voluntary codes of conduct, appropriate legislations and compliance with internal SOPs.
- Mentoring and coaching direct reportees, if any.
Qualifications:
Bachelor's degree required; advanced degree preferred (e.g., MS, Ph.D., or MD).
Minimum 3 years of medical affairs, medical writing, patient access, and advocacy experience in the biopharmaceutical industry.
Salary: $80,000 - $100,000 per annum.
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