clinical documentation

Senior Manager, Clinical Contracts – EMEAIn order to make an application, simply read through the following job description and make sure to attach relevant documents.Location: Brussels, BelgiumAdditional Location: Antwerp may be considered depending on candidate profileEmployment Type: Permanent, Full-TimeWorking Arrangement: Hybrid, with regular site...

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life...

Join a clinical research team dedicated to generating high-quality clinical evidence that advances patient care. In this role, you will support the successful execution of clinical studies across Europe by coordinating essential clinical trial activities, maintaining study documentation, and partnering with cross-functional teams around the globe. This is an...

Cochlear Limited in Mechelen, Belgium is seeking a highly organized Clinical Trial Assistant for a one-year fixed-term role within the Clinical Operations team. You will support planning, execution and documentation of international clinical trials, coordinating with CPMs, CRAs, sites and external partners to ensure compliant, efficient study conduct.The...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across...

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the...

Clinical Study Associate I Are you passionate about clinical research and interested in contributing to work that improves human health? If so, this opportunity may be a great fit for you. CellCarta is seeking an entry-level Clinical Study Associate (CSA I) to join our dynamic team in Wilrijk, Antwerp. As a leading clinical research organization, we are...

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to...

Are you an experienced freelance CRA and have full-time availability for a project to start asap? You will be welcomed in a global company in which team spirit is key. Job Description As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety...

IQVIA is seeking a senior FTE Medical Writer to deliver clinical documents including CTRs, TDOs/CTPs, CTP amendments, Briefing Books, IBs and IB updates, and submission sections for eye health and inflammation programs.The writer will be embedded in sponsor processes, participate in planning and meetings, and follow sponsor SOPs, EDMS workflows, and...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

CellCarta is seeking a Clinical Study Specialist I to ensure site-level regulatory documentation, monitoring visits, and close-out activities are executed with precision. You will liaise with Project Management, Regulatory Affairs, and QA to maintain audit readiness across oncology trials.The role requires 2+ years in clinical research, GCLP/GDP knowledge,...

Syneos Health, Inc. is seeking a Principal I/II Medical Writer for fully remote work across Italy, UK, Spain, Poland or Ireland. The role focuses on regulatory submissions and clinical documentation support within our Clinical Solutions team.The position offers broad exposure to drug development programs and collaboration with cross-functional teams while...

Alsinova in Belgium is seeking Medical Writers to join our consulting team for client projects across pharma and biotech. You will synthesize literature, draft, edit and update clinical development documents with high technical accuracy.The ideal candidate has at least 1 year of Medical Writing experience, strong English and French writing skills,...

PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. PSI is a leading Contract Research Organisation with 30 years in the industry, offering a...

Clinical Study Specialist I  Are you a clinical operations professional who thrives on precision, compliance, and process efficiency? We are looking for an energetic Clinical Study Specialist I to join our growing Clinical Operations team and support the successful execution of innovative oncology clinical trials. Summary In this role, you will be...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

Non-Clinical Safety Lead To strengthen our Non-Clinical Safety Evaluation group within Early Clinical Development and Translational Science, we are looking for a talented individual for the role of Non-Clinical Safety Lead, based in Braine L'alleud, Belgium or Slough, UK or Cambridge, MA (USA). About The Role As a Non-clinical Safety Lead, you will provide...

Your mission: As a Clinical Project Manager at Cascador/moveUP, you will be responsible for the management of the clinical trials of our partners, ensuring their smooth progress and managing upcoming clinical trials, with the use of our next-generation eCOA/eDiary Platform. You will be in direct contact with our sponsors, academic centers and sites using our...

Don't see an opening that quite matches what you're looking for, or not ready to make a move yet? Let us know! We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the Process Looks Like A Talent Acquisition...