Senior Medical Writer — Remote, Part‑Time, Regulatory

Syneos Health, Inc. is seeking a Senior Medical Writer to join the Europe home-based FSP team. You will lead medical writing deliverables across studies, ensuring scientific clarity and regulatory compliance while coordinating with cross-functional teams. The role is full-time, remote across Europe, with potential for modest travel. We value experience in...

Principal Medical Writer / Sr Principal medical Writer- Sponsor-dedicated Updated: Today Location: Remote, Spain Job ID:25113363-OTHLOC-3529-2DMAD-2DR Description Principal Medical Writer / Sr Principal medical Writer- Sponsor-dedicated Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We...

Senior Medical Writer - Europe / home based - FSP Team Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources...

JOB DESCRIPTION Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where...

ICON Clinical Research is seeking a Senior Medical Writer to lead medical writing strategies for clinical projects. You will own regulatory documents, contribute to protocol and CSR development, and mentor junior writers while coordinating with study teams to meet timelines. The role requires strong regulatory expertise, high-quality writing, and...

About the Role We’re looking for a Senior Game Developer to bring fresh ideas, strong technical expertise, and a passion for building high-quality games. This role is ideal for someone who enjoys working close to the engine, developing new features, and continuously improving performance and scalability. You’ll be part of a team that values ownership,...

Work as a senior data coordinator on clinical and non-clinical trials; producing and validating eCRFs and databases to excellent quality whilst adhering to deliverable timelines. Producing, reviewing and updating eCRF specifications and sections of the Data Handling Manual. Leading clinical coding activities and management of third party data and eCRFs in...

Senior/Principal Statistical Programmer SAS + R (Remote) Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is...