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Responsible for development, review, finalization, and maintenance of clinical trial documents such as informed consent form and other relevant documents

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Centralized Trip Report Reviewer I

Covance India Pharmaceutical Services Private Limited
Bengaluru / Bangalore Mumbai
7-9 years
Not Specified

Management of complex projects under direction of a Project Manager / Director as assigned.

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Operate in accordance with the Adjudication Services Operational Plan in place on assigned project(s).

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Experience with writing, editing and executing automated validation scripts manually and/or using automated tools

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5 Years work experience in Clinical research including a strong working knowledge of the ICH - GCP guidelines and FDA, GMP regulations.

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Responsible for Detailed performance review and Management of Direct reports including: Annual Performance Management & Development(PMD), Individual Development Plan (IDP), Line of sight goals, Shoves & Tugs.

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Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines.

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Management of complex projects under direction of a Project Manager / Director as assigned.

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Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines.

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4 - 6 years of relevant work experience to include data management and database support: EDC systems programming or SAS programming.

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