Clinical Trial Educator

The CTSC collaborates with global and country teams to ensure all information and documentation for the submission to EMA Clinical Trial Information System (CTIS) are provided in a timely manner basis throughout the lifecycle of a clinical trial. Principal Responsibilities: 1 Lead the operational EU CTR Submission strategy development, planning and...

Johnson & Johnson, through its operating companies, is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. We strive to provide scientifically sound, high quality products and services to help heal, cure...

Johnson & Johnson is recruiting for an Analyst II, Trial Supply Planner to be located in Beerse, Belgium. Remote work options may be considered on a case-by-case basis and if approved by the company. For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business...

**About Johnson & Johnson** We are looking for a Trial Supply Planning Lead. This individual contributor is responsible for planning the Pack & Label and Distribution activities of Patient Kits to meet First-Patient-In (FPI) date and consistently meet Successful Patient Dose target throughout the lifecycle of a J&J Pharma R&D trial, within budget....

Within our Clinical & Statistical Programming (C&SP) organization we are looking for experienced individuals with in-depth programming and visualization competencies to join our Clinical Data Analytics & Reporting (CDA&R) team. This is an exciting opportunity to be part of an innovative group that is pivotal in defining our next generation data and...

We are looking for a driven Senior Site Manager (Clinical Research Associate) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in Late Development (phase 1b-2-3). As Senior Site Manager, you will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating...

We are looking for a driven Senior Site Manager (Senior Clinical Research Associate) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in Late Development (phase 1b-2-3). As Senior Site Manager, you will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating...

The Scientist Clinical Pharmacokinetics (PK Scientist) role within Clinical Pharmacology and Pharmacometrics (CPP) responsible for (in collaboration with the CPP Leader), the following activities of end-to-end Phase 1 study execution of Clinical Pharmacology Phase 1-owned studies including: protocol development, pharmacokinetic/pharmacodynamic data analysis,...

The Clinical Pharmacology (CP) PK Scientist role within Clinical Pharmacology and Pharmacometrics (CPP) is responsible for (in collaboration with the Clinical Pharmacology Leader), the following activities of end-to-end Phase 1 study execution of Clinical Pharmacology Phase 1 studies including: protocol development, pharmacokinetic/pharmacodynamic data...

Johnson and Johnson is currently seeking a **Director, Clinical Research Equity **located in Beerse, Belgium; Basel, Switzerland; OR High Wycombe, United Kingdom. For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the...

**Position Summary**: The Program Development Leader (PDL) is accountable for the operational execution of the Clinical Development Plan (CDP). As a disease area thought partner, the PDL is responsible for the development of the program-level strategy and ensuring cross-functional alignment, identifying, and resolving program-level risks that may impact...

We are looking for a driven Senior Site Manager (Clinical Research Associate) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in Late Development (phase 1b-2-3). As Senior Site Manager, you will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating...

Het Clinical Distribution Team binnen de DELIVER afdeling van Johnson & Johnson werft kandidaten voor een Customer Service Medewerker Clinical Distribution (M/V/X) voor de locatie Beerse. Wat je zal gaan doen: Je komt als Customer Service Medewerker Clinical Distribution terecht in het Clinical Distribution team binnen de DELIVER afdeling van Johnson &...

J&J Innovative Medicine is recruiting for a Team lead Clinical Distribution, located in Beerse, Belgium. As team lead within the Clinical Distribution team, you'll be part of Distribution Network team at DC Beerse within J&J DELIVER EMEA. This dynamic and motivated team of ~12 distribution specialists coordinates up to 250 clinical trials which are...

We are looking for a driven Senior Local Compliance Specialist to join our Clinical Operations team in Belgium and The Netherlands but also supporting the local compliance team in The Nordics (Sweden, Denmark and Finland). You will contribute to a coordinated and comprehensive local quality and compliance approach to ensure our clinical trials will be...

Johnson & Johnson is currently seeking a **Senior Site Manager **ED&CP **to your our team in Beerse, Belgium. A Senior Site Manager ED&CP may contribute to process improvement, training and mentoring of other Site Managers. **Principal Responsibilities**: Participates in site assessments, conducts pre-trial site assessment visits and/or participates to...

Johnson & Johnson is currently seeking a Clinical Forecasting Specialist (CFS), located in Belgium. Your key responsibilities: - Leading validation of drivers, reconciling and maintaining data accuracy for Planisware and UCT systems as well as providing insightful decision support using reporting platforms (e.g. Tableau, Spotfire, UCT, Viz Café) for...

Essential tasks and responsibilities: Leading the Operational QA groups in the pilot plants of Beerse, Schaffhausen and Leiden Advanced Therapies to ensure that the GMP activities as manufacturing, packaging and labelling of Investigational Medicinal Product (IMP) can be carried out as required by legislation and ensures quality and compliance of the IMP...

**Statistical Programming Lead - Integrated Data Analytics and Reporting (IDAR)** **Position Summary**: The Statistical Programming Lead is an experienced Statistical Programmer with advanced knowledge of statistical programming methods, languages and data structures and capabilities in leading analysis and reporting activities and programming teams in...

Position Summary: The Innovative Health (IH) Organization has been created to drive meaningful impact to participant health and wellbeing by reinventing the clinical trial experience. The Innovative Health organization connects teams across development to novel capabilities and solutions, unleashing the potential of innovation to drive broader access to...