parexel

Parexel FSP is hiring a CRA to be home-based in Poland (Trojmiasto/ Koszalin). You will manage oncology site activities, ensure trial integrity, and collaborate with leading experts. The role emphasizes independent site monitoring, strong organization, and the ability to travel as needed.You will join a sponsor-dedicated team with competitive compensation,...

Parexel in Warsaw offers a Regulatory Affairs Consultant role that can be home or office-based. You will bring a few years of Regulatory Affairs experience with CTA submissions from Europe, supporting Parexel and client work. Under a Project Lead you ensure timely, high-quality client deliverables and receive mentoring for complex tasks.The role emphasizes...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Parexel is seeking an experienced Clinical Research Associate to join our Multi-Sponsor Clinical Trials Team in Poland. As CRA, you will build and maintain site relationships, oversee trial delivery from start-up to close-out, and be the single point of contact for sites.Parexel offers world-class tech and training, reduced travel, and a bonus program for...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Parexel FSP in Poland is seeking a remote CRA to manage oncology studies for a single client from a home-based base in Poland. You will supervise site activities, ensure adherence to protocol, and collaborate with industry experts to drive successful outcomes.This role offers a premium salary, attractive benefits, and opportunities to travel and develop your...

Parexel is seeking a Site Contract Associate to support clinical trial site agreements from a home-based role in Poland. You will draft and negotiate contracts, align them with local regulations, and manage the contract lifecycle across regions.You will collaborate with internal teams and external sites to ensure timely, compliant contracting while...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions. The role supports Regional Intelligence, Site Intelligence and Feasibility projects, handling multiple studies and ensuring high-quality data delivery for cross-functional stakeholders.We seek professionals with 2-3 years in clinical...

Parexel FSP in Poland is hiring a Clinical Study Administrator to support study coordination from start‑up to close‑out. The role is based in Warsaw three days a week, with opportunities for progression within a global CRO environment.The CSA will handle trial/site administration, document management, regulatory responsibilities, and budgeting. English...

Parexel is seeking a Director, AI Platforms in a remote role based in Poland or Romania. You will lead platform engineering that powers enterprise AI delivery, owning AI-first stack, environment management, and orchestration while partnering with engineering and compliance teams.You will recruit and mentor a small team of senior ICs, balance vendor...

Parexel is seeking an Investigator Payments Lead – Senior Associate for a remote, 6-Month Fixed Term Contract. You will ensure timely and accurate payments to clinical trial sites and investigators from start-up to closeout, supporting the sponsor’s Clinical Development & Operations through a Functional Service Provider model.Join a fast-paced,...

Parexel FSP in Warsaw, Poland, seeks a Clinical Trial Coordinator to support the study lifecycle from start-up to closure. This office-based role collaborates with the Clinical Research Manager and other team members to ensure smooth site operations and regulatory compliance.The ideal candidate has 1–2 years coordinating clinical trials, fluent Polish plus...

About Parexel Parexel is a leading global clinical development partner delivering insights-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...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

Parexel is seeking a Medical Writer II to join our team across Poland, Spain, Romania, or Serbia. You will support high-quality clinical and regulatory documents, including CTRs, CTPs, IBs, and submission materials, ensuring timely preparation and coordination.You will work with cross-functional teams, manage document timelines, coordinate reviews, and...

Parexel is seeking a Senior Medical Writer to support the development of high-quality clinical and regulatory documents. This embedded role involves coordinating CTRs, CTPs, IBs, and submission documents, while managing timelines and ensuring quality and compliance across the document lifecycle.You will work with cross-functional teams to prepare, review,...

Parexel is seeking a Documentation Specialist / Medical Writer to join a distributed team across Poland, Spain, Romania or Serbia. You will develop and finalize clinical and regulatory documents and manage document workflows within an electronic system, ensuring timely submissions and adherence to quality standards.You will collaborate with cross-functional...