Freelance Document Submission Staff

Job Title: Regulatory Submission SpecialistWe are seeking a highly skilled Regulatory Submission Specialist to join our team. The ideal candidate will have extensive knowledge of EU Clinical Trial Applications and experience in regulatory document management.Key Responsibilities:Ensure technical compliance of clinical trial submissions via smooth information...

Job DescriptionThis role involves overseeing the creation and formatting of documents, including dossiers, reports, and submissions, to ensure compliance with regulatory guidelines.The Senior Electronic Document Specialist will work in a fast-paced environment and be responsible for managing electronic documents throughout the preparation process, including...

Regulatory Writing ManagerThis is a critical role that involves crafting and gaining approval for scientific and regulatory submission documents in line with global regulatory standards.Key Responsibilities:Develop regulatory submission documents, including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol...

About the RoleAs a Clinical Trial Submission Management Specialist, you will be responsible for ensuring Clinical Trial Application approvals in the EU throughout the whole study lifecycle. This involves working closely with cross-functional teams to ensure compliance with EU regulations and guidelines.Key responsibilities include preparing submission...

Career Category RegulatoryThe Senior Associate Global Submission Management Americas will help ensure the smooth compliant flow of information between all functional areas internal and external to GRAAS including local offices external partners and regulatory authorities within the North American context This role leads the creation of regulatory...

Job DescriptionRoles & Responsibilities:- Lead/support various Clinical Trial and Marketing Application type submissions and associated Global/Submission Content Plans.- Participation in information system and software update projects as well as ongoing system validations- Serve as point of contact between Amgen's functional contributors and external...

Job DescriptionRoles & Responsibilities:- Be assigned to one or more Amgen products under development to ensure Clinical Trial Application approvals in the EU throughout the whole study lifecycle. As technical experts in the EMA Clinical Trial Information System (CTIS), ensure compliance with the EU Clinical Trials Regulation (EU CTR) for every Clinical...

Freelance Event Executive / CoordinatorWe are seeking experienced Freelance Event Professionals to join our on-ground team for exciting events across the city.As a Freelance Event Executive / Coordinator, you will be responsible for overseeing event setup and execution, coordinating with vendors, staff, and clients, managing crowd control, registrations, and...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...