EU CTR Submission Specialist - Warszawa

Bristol Myers Squibb is a company that offers challenging and meaningful work opportunities. The company recognizes the importance of balance and flexibility in its work environment. · Management supports end-to-end regulatory activities for assigned projects. · ...

The EU CTR Submission Specialist is responsible for planning and managing regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). ...

Here you'll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. · Collaborate with stakeholders to define eCTD submission strategies document requirements ensuring alignment with regulatory standards project timeline ...

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. ...

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential jobs which require 100% of shifts onsite at your assigned facility. · ...

Working at Bristol Myers Squibb is a unique opportunity to transform patients' lives through science. · ...

We are recruiting for a Regulatory Affairs Senior Specialist – Publishing to join a growing Regulatory Publishing team at an international Contract Research Organization. · This role can be based remotely (home based) from anywhere in Poland or Bulgaria. · ...

Due to ongoing global expansion Indero is looking to hire a Regulatory Affairs Specialist responsible for preparation and submission of part I and/or part II following EU CTR and other applications created within or outside of the company. · ...

Due to ongoing global expansion Indero is looking to hire a Regulatory Affairs Specialist responsible for preparation submission of regulatory documents submissions in assigned countries ensuring high quality standards coordination of regulatory timelines deadlines for all assign ...

A Finance Operations Specialist will support operational tasks related to E-Billing invoice submission. · ...

+The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. · ...

E-Billing Specialist: Manage end-to-end E-Billing process, ensure billing accuracy, monitor platforms. · ...

Astrellas bietet eine inspirierende Arbeitsumgebung an und ermöglicht es den Mitarbeitern Gutes für Andere zu tun. · ...

Freyr is a fast-growing company specializing in regulatory solutions for the Life Sciences industry. · ...

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. · ...

Roles within the Site Start-Up/Site ID job family are responsible for managing and executing the site identification process in accordance with regulations, SOPs, and project requirements. · ...

The Apparel Color Specialist ensures color accuracy and consistency by evaluating supplier submissions against established standards. · The role supports product quality seasonal timelines design production decisions. ...

We are seeking a Regulatory Affairs Specialist to support the Professional Hygiene and Home Care regulatory programme. · ...

This E-Billing Finance Operations Specialist will support operational tasks related to E-Billing invoice submission. · ...

+Job summary · De Gruyter Brill is seeking a Marketing Manager to join the existing team to develop analytical and product insights for our global marketing teams. · +ResponsibilitiesTrack and report on a range of product and marketing KPIs, · Enhance author engagement initiative ...

As a Study Start-Up Specialist at IQVIA Biotech in Poland, you will partner with biotech companies to transform innovation into patient impact. You will perform tasks associated with Site Activation (SA) activities and work with projects under general supervision. · ...