Senior Clinical Trial Liaison Lead

About ParexelParexel is a leading global clinical development partner delivering insight-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care...

Parexel is seeking a Global Patient and Site Engagement – Clinical Trial Liaison to join our Spain team in a remote/home-based capacity. You will engage sites and patients, build relationships with investigators, and support operational excellence to ensure studies are compliant and patient-focused.The role emphasizes cross-functional collaboration,...

TFS Health Science invites a Freelance Clinical Database Programming Process Lead to join our CDS Group Management team. This 1.0 FTE role focuses on building a scalable DBP capability, defining governance, and guiding validation, testing and documentation across multiple EDC platforms. Based remotely across the UK, Germany, Poland, Portugal, Spain or...

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...

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of high-quality clinical study documents in Spain. This role requires planning, writing, editing, and QC of documents like protocols, IBs, CSRs, and narratives with strict adherence to regulatory guidelines.You will ensure alignment with ICH, FDA,...

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...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.Essential Functions of the job: Preferred location:...

Start Up Lead Home based MadridAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

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...