...plain text, focused on key accountabilities or duties.
Ideally no more than 75 words.
Avoid internal jargon or acronyms.
The Specialist supports the planning, organization, and review of routine submissions...
...The Document Coordinator is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
The Document Coordinator will interact with cli...
Directly supports electronic submission of regulatory documents / applications including IND, CTA, NDA, BLA, MAA, etc. through formatting, processing, and compilation of Word and PDF documents to the appropriate client specifications.
Formats a...
...Employment Type: Full Time, Permanent
Education
UG: Any Graduate
PG: Any Postgraduate, MBA/PGDM in Any Specialization
Doctorate: Doctorate Not Required
Skills: regulatory affairs,publishing,electr...
...regulatory submissions and activities for products throughout the life-cycle of a product in compliance with Health Canada regulatory requirements... ...to junior staff in the creation of sub...
...for CT under the EU Regulation.
Position Responsibilities
Manage the signing of clinical trial documentation such as powers of attorney, expected to be able to coordinate many signing at the same time.
Prov...
...and build upon each other to achieve results
Minimum Qualifications
Bachelor s degree in statistics, biostatistics, mathematics, computer science or life sciences required
At least 8 years programming exper...
...listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, the Sandoz associates. This...
...reconciliation to ensure timely submissions are in accordance with FDA regulations as well as meeting all Novartis requirements for submission-related activities
Proactively identify issues, gaps, and trade-offs ...
