Principal Medical Writer: Regulatory Submissions Lead

Principal Medical Writer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking Senior or Principal Medical Writer to join our...

**Certara**: Certara (CERT) is the largest and most comprehensive provider of strategic drug development, modeling & simulation and regulatory science services. We partner with biopharmaceutical businesses to optimize drug development decisions and accelerate the drug development process. At Certara, you will play an important role helping our clients...

Principal Medical WriterICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking Senior or Principal Medical Writer to join our...

**At Certara, we accelerate medicines to patients by partnering with life science innovators.** **Certara**: Certara (CERT) is the largest and most comprehensive provider of strategic drug development, modeling & simulation and regulatory science services. We partner with biopharmaceutical businesses to optimize drug development decisions and accelerate the...

A global biopharmaceutical services company is seeking a Medical Writer to support clinical documentation and regulatory submissions. The ideal candidate should have a Bachelor's in Life Sciences, significant experience in medical writing, and strong interpersonal skills. This role involves authoring Clinical Study Reports, managing documentation quality,...

When our values align, there's no limit to what we can achieve.Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. We believe in our values,Parexel are recruiting for either a within our groupThe FSP...

This role is for one of the Weekday's clientsMin Experience: 8 yearsLocation: EuropeJobType: full-timeWe are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory operations and system implementations. The ideal candidate will play a critical role in managing...

A cutting-edge medical technology firm in Paris seeks an experienced Regulatory Affairs professional to develop innovative regulatory strategies for AI/ML-enabled medical devices. This role involves preparing submissions, serving as a liaison with regulatory bodies, and ensuring compliance. Ideal candidates will have over 6 years of relevant experience,...

Senior Medical Writer ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Medical Writer to join our diverse and...

Cmed is seeking a Medical Writer with regulatory medical writing experience for this client dedicated opportunity. Experience with at least 2 of the documents: abbreviated protocol, protocol, and subsequent amendments, amended protocols, clinical study reports (all phases), lay summary of results, narratives, Clinical modules of CTDs, Q&A, P70, investigators...