Key Accountabilities: He should be responsible for authoring clinical evaluation reports, clinical evaluation plans, post-market surveillance reports, and periodic safety update reports He must be fully aware of the literature search, screening, and summarization of articles He must know how to perform data fact check of the documents authored Ensure documents comply with the client/regulatory requirements Participate in client calls per project requirements Compliance to quality, confidentiality, and security He should adhere and follow quality systems, processes and policies He must comply to training and specifications PAN INDIA
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