Senior Regulatory Translation Project Lead – Submissions

A leading global clinical research firm in Barcelona is seeking a Senior Translation Project Manager to oversee Regulatory Submissions for Marketing Authorization translation and localization. The ideal candidate will have over 4 years of project management experience in the Language Services industry and be well-versed in client management and regulatory...

Senior Translation Project Manager – Regulatory SubmissionsJoin to apply for the Senior Translation Project Manager – Regulatory Submissions role at IQVIA.SENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONS Working with the wider Project Management team, the Senior Translation Project Manager – Regulatory Submissions is responsible for...

SENIOR TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONSWorking with the wider Project Management team, the Senior Translation Project Manager – Regulatory Submissions is responsible for coordinating and managing the full lifecycle of Regulatory Submissions for Marketing Authorization translation and localization projects to completion whilst ensuring...

A biopharmaceutical solutions organization is seeking a Senior Regulatory Medical Writer to lead medical writing deliverables and coordinate regulatory submissions. This remote position involves managing documents and mentoring junior writers while ensuring compliance with regulatory standards. Ideal candidates have proven expertise in medical writing,...

SENIOR TRANSLATION PROJECT MANAGER  Working with the wider Project Management team, the Senior Translation Project Manager is responsible for coordinating and managing the full lifecycle of translation and localization projects to completion whilst ensuring IQVIA's standards are met.  •    Manage multiple translation and localization projects at any...

Position Title: CMC RA Expert Location: Barcelona Type of Contract: Full-Time / On site PharmEng Technology, an Efor Group of Companies, is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and...

Position Title: CMC RA Expert Location: Barcelona Type of Contract: Full-Time / On site PharmEng Technology, an Efor Group of Companies, is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our dedication to quality, safety, and...

Role holders expertly drive strategic communications excellence to achieve successful submissions and approvals. They develop innovative best practices and improvement initiatives. **Typical Accountabilities** The Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important...

#LI-onsite At CooperSurgical, we are currently looking to recruit a Regulatory Affairs Specialist to join our Global Regulatory Affairs team. This role focuses primarily on the US (FDA), Canada (Health Canada) and Australia (TGA) markets, ensuring compliance and supporting submissions that enable patients and healthcare professionals to access our innovative...

Regulatory Affairs ExpertJob Description:Position Title: CMC RA ExpertLocation: BarcelonaType of Contract: Full-Time / On sitePharmEng Technology, an Efor Group of Companies, is a leading pharmaceutical and biopharmaceutical consulting company committed to providing innovative solutions to the challenges facing our industries. We pride ourselves on our...