The Associate Clinical Project Manager (Sponsor dedicated) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP
Company Description 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
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)
What Youll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given
Snr CRA - Clinical Site Management ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Clinical Research Associate (CRA) - Belgique / België Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a (Senior) Clinical Research Associate in our client dedicated FSP team - Belgium – Make an Impact at the Forefront of Innovation We have successfully supported the top
Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the
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
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
Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based For candidates able to start before December 2026, a discretionary sign‑on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at
Clinical Research Associate II - Sponsor dedicated - Belgium - Home based For candidates able to start before December 2026, a discretionary sign‑on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at
Our client, a global leader in the MedTech industry, is looking for a Senior Clinical Research Associate to support clinical study activities within a MedTech environment. The successful candidate will be responsible for managing clinical activities at study sites conducting
We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance
We are looking for a motivated Clinical Research Associate (CRA) to support the successful execution of clinical studies within an innovative MedTech environment. In this role, you will be responsible for monitoring clinical trial activities across multiple study sites, ensuring
Work ScheduleStandard Office Hours (40/wk) Environmental ConditionsOffice Job Description Join us as a Manager Project Management - Labs – And lead our team to ensure the successful execution of projects, drive operational excellence, and deliver high-quality results. At
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Regulatory Affairs Associate Director - EU Regulatory Lead– Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and
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
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