Regulatory Medical Writing Operations Lead

**𝗘𝘅𝗰𝗹𝘂𝘀𝗶𝘃𝗲 6 𝗠𝗼𝗻𝘁𝗵 𝗖𝗼𝗻𝘁𝗿𝗮𝗰𝘁 (20 hours) – 𝗠edical Writing Operations Lead – Remote, 𝐔𝐊 **Are you an experienced Medical Writing Operations Lead passionate about pioneering therapies in the biotech industry? Join our innovative client, a pioneer in developing revolutionary CAR-T...

**𝗘𝘅𝗰𝗹𝘂𝘀𝗶𝘃𝗲 6 𝗠𝗼𝗻𝘁𝗵 𝗖𝗼𝗻𝘁𝗿𝗮𝗰𝘁 (20 hours) – 𝗠edical Writing Operations Lead – Remote, 𝐔𝐊 **Are you an experienced Medical Writing Operations Lead passionate about pioneering therapies in the biotech industry? Join our innovative client, a pioneer in developing revolutionary CAR-T...

**𝗘𝘅𝗰𝗹𝘂𝘀𝗶𝘃𝗲 6 𝗠𝗼𝗻𝘁𝗵 𝗖𝗼𝗻𝘁𝗿𝗮𝗰𝘁 (20 hours) – 𝗠edical Writing Operations Lead – Remote, 𝐔𝐊 **Are you an experienced Medical Writing Operations Lead passionate about pioneering therapies in the biotech industry? Join our innovative client, a pioneer in developing revolutionary CAR-T...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

Medical Writer - Contractor Department: Clinical Development Employment Type: Contract / Temp Location: invoX Remote (Rest of world) invoX is a research-driven global biopharmaceutical company using next-generation technology platforms to discover and develop innovative medicines that can change the lives of people around the world. Our vision is...

Parexel is seeking highly motivated and experienced individuals for the position a Senior Regulatory Affairs Associate. This role can be home, or office based in various locations in Europe . As part of our team, you will have the opportunity to work within a collaborative environment and deliver services within your technical expertise. Join us and make a...

Xstrahl is a leading medical technology company that designs and manufactures Medical X-ray Systems used in treatment of cancers and dermatological disorders, as well as a pioneer in the development of advanced X-ray systems for pre-clinical radiation biology research. We are looking for a QARA Engineer who can work as part of the R&D team and support the...

We are looking for a Medical Lead Auditor who will be responsible for the conduct of management system auditing (both scheduled and unannounced) of Medical Device Manufacturers and for conducting audits in accordance with Intertek’s established procedures whilst maintaining a high standard of service delivery. As the Medical Lead Auditor, you will have...

We are looking for a Medical Lead Auditor who will be responsible for the conduct of management system auditing (both scheduled and unannounced) of Medical Device Manufacturers and for conducting audits in accordance with Intertek's established procedures whilst maintaining a high standard of service delivery. As the Medical Lead Auditor, you will have...

Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team. Position...

Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team. Position...

Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remoteCompany Description:We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.Position Overview:As a...

Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remote Company Description: We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies. Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team. Position Overview:...

Medical Writer - Contractor Department: Clinical Development Employment Type: Contract / Temp Location: invoX Remote (Rest of world) Reporting To: Robert Ilaria Description invoX is a research-driven global biopharmaceutical company using next-generation technology platforms to discover and develop innovative medicines that can change the lives of...

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. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

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. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

Corinium Centre, Love Lane Industrial Estate, Cirencester GL7 1YJ, UK Req #233 04 April 2024 Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards,...

Lead with Impact: Join Bioscript Group as a Medical Team Lead Ready to make a difference at the forefront of medical communications? Bioscript Group is searching for a dynamic Medical Team Lead to join our passionate team in the UK. As a Medical Team Lead with us, you'll play a pivotal role in providing operational leadership to internal teams and...

Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device Associate Main Purpose of Job and Objectives: Perform Regulatory tasks to ensure compliance with regulations. Prepare regulatory documentation and submissions for product approvals. Develop regulatory plans/strategies for new products and changes to existing products. ...

WANTED: Senior Editor (maternity cover), The Lead We're looking for someone to step in to help lead our editorial agenda, from commissioning and editing, to writing and strategic planning. Is this you? Apply below.  The Lead - Senior Editor (maternity cover) part-time/on-site  Location : London office Position : Part-time, maternity cover, 6-month...