Senior Clinical Trial Liaison Lead

Position Summary The Senior Medical Writer/Principal Medical Writer will be responsible for leading the development of high-quality and on-time clinical study documents.Specific responsibilities include clinical document planning, writing, editing/formatting, and performing QC review.Develops documents in compliance with Precision MW Style Guide, Precision...

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...

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...

This position is listed on behalf of a partner company, who manages all applications and next steps.Our partner is looking for a Epic Project Manager based in Spain.This is a senior project management role focused on delivering complex Epic and healthcare IT initiatives from planning through stabilization.You'll lead implementations, Community Connect...

Parexel International is recruiting for a Global Patient and Site Engagement – Clinical Trial Liaison in Spain.This fully remote home-based role involves engaging with KOLs, PIs, and HCPs in Oncology, driving site and patient engagement strategies, and supporting clinical operations.A strong scientific background in oncology and MSL-like experience are...

Thermo Fisher Scientific is seeking a Senior Clinical Safety Lead to manage and coordinate medical safety projects across studies, ensuring compliance and alignment with contracts.You will lead clinical monitoring activities, review safety data, and serve as the primary contact for project teams and alliance leads.The role requires substantial experience in...

Emergo by UL's Human Factors business unit is a global leader in Human Factors Engineering (HFE) services, with team members in the US, Europe, and Asia.Emergo by UL's HF staff consists of human factors professionals who perform research, design, and usability studies primarily for the medical and pharmaceutical industries.We are seeking a service-minded,...

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of high-quality clinical study documents in Spain.You will plan, write, edit, format, and QC protocols, IBs, CSRs and associated narratives with regulatory-compliant content and eCTD readiness.The role requires 5+ years as a Senior Medical Writer or...

Premier Research is looking for a Senior Regulatory Submissions Lead to join our Regulatory Submissions and Contracts team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics.What we do is profoundly connected to saving and improving lives, and we...