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Alcon

Sr. Associate, Clinical Research (Non-MD)

Bangaloreonsitesenior

Posted today · via Workday

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About this role

Key Responsibilities: 1. Author, co-author, and support updates to CEPs, CERs, PMCF Plans and Reports, SLR protocols/reports, and related clinical evaluation documentation for assigned medical device products. 2. Apply clinical evaluation requirements, internal procedures, templates, and evidence appraisal expectations to produce clear, traceable, scientifically sound, and audit-ready deliverables. 3. Ensure clinical evaluation deliverables are developed in alignment with EU MDR 2017/745 , applicable MDCG guidance , MEDDEV guidance where relevant, internal procedures, and other applicable regulatory, clinical evaluation, and post-market guidance. 4.…

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1

Skills match

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2

Level fit

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3

Domain experience

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4

Recency

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5

Location fit

This role is based in Bangalore. We weight your proximity and willingness to relocate.

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