Senior Analyst Clinical Supplies Study Master R&d

Clinical, Regulatory AffairsWe are a fast-growing consultancy assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European regulations.We provide practical solutions in the area of regulatory affairs and quality assurance. We help with the implementation of quality systems, technical documentation and the...

QbD clinical Belgium Clinical Table of Contents Do you want to make an impact as Clinical Research Professional? Do you want to protect the safety & well-being of subjects and guarantee data quality? Do you get energy from daily communication with investigators, study coordinators and study teams? Do GCP ICH E6 R2 and ISO 14155 have no...

Johnson & Johnson is recruiting for a Manager Clinical Supply Integrator, to be located in Titusville, New Jersey; Wayne, PA; or Antwerp, Belgium. This matrix team leader is responsible for end-to-end supply chain management of clinical supplies. Through the Clinical Supply Sub-Team develops supply strategies matching needs of clinical programs and trials...

**Senior Statistical Programmer Analyst - Integrated Data Analytics and Reporting (IDAR)** **Position Summary**: The Senior Statistical Programmer Analyst is an individual contributor with in-depth knowledge of statistical programming methods, languages and data structures who supports data analysis and reporting activities within the Statistical...

Founded in April 2014 in Grenoble (France) as a spin-off of the French Blood Bank (Etablissement Français du Sang, EFS), PDC*line Pharma is a Belgian-French biotech company that is developing a **novel class of off-the-shelf cancer immunotherapies** based on a proprietary Plasmacytoid Dendritic Cell line (PDC*line) pre-loaded with peptides that are derived...

We are looking for an R&D Master Data Manager to support the implementation Johnson & Johnson is seeking an outstanding individual to join our team as an IM Transcend Master Data Manager for R&D. The location of this position is Beerse, Titusville, Horsham or Malvern. At Johnson & Johnson, we believe health is everything. Our strength in healthcare...

**ITM vacancies**: Project coordinator epidemiological study Department of Public Health Epidemiology and Disease Control **Introduction**: The Institute of Tropical Medicine (ITM) in Antwerp aims at the advancement and spread of science that contributes to infectious disease medicine and to public health globally with focus on low - and middle income...

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,...

QbD clinical Belgium Clinical Table of Contents QbD Clinical, part of the QbD group, continues to grow and we are looking for a new colleague who will support us as CTA. What are your main responsibilities? The Clinical Trial Assistant is responsible to assist the Clinical Research Professional (CRP) in the conduct of clinical...

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...

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...

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...

Clinical Belgium Clinical, Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations .  Our objective is to provide manufacturers with practical solutions in the area...

Description: **Location**: Antwerp area, Belgium - office based **Schedule**: Full-time, permanent Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds. TalentSource Life Sciences (the...

As a global Research Organization to the biopharmaceutical industry, **CellCarta (formerly Caprion - HistoGeneX)** provides access to a broad offering of biomarker platforms and services. We partner with our clients to address the most complex scientific testing needs, delivering customized biomarker testing solutions to further the limitless potential of...

Clinical Trial Manager Our client is looking for an experienced Clinical Trial Manager (CTM) to work with a fast rapidly growing organisation. Location: Antwerpen area Start: Mid October Duration: 8 months Type: Freelance Contract Responsibilities may include: - General day to day management of the trial - Weekly reports on the trial team conducted...

**Precision for Medicine is not your typical CRO.** Becoming a member of our growing team, means you will be embarking on an opportunity to work with leading Oncology experts with a niche precision medicine company. We stand out from the crowd with an unusual value proposition; focusing exclusively on Oncology clinical trials that incorporate the use of...

Clinical Belgium Table of Contents Do you want to make an impact as Senior Operations Lead, Clinical Division? Do you get energy from daily communication with study teams and clients? Do the cornerstones of Operations within Clinical Development have no more secrets for you? Then you might be the Senior Operations Lead, Clinical Division we...

Johnson & Johnson is seeking an outstanding individual to join our team as a Manager IM Transcend Advanced Therapies and Clinical Manufacturing for R&D. The location of this position is Beerse, Titusville, Horsham or Malvern. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...

Job SummaryAs a Senior Regulatory Affairs Expert IVD, you will be responsible for managing projects on clinical evidence and technical documentation, ensuring high-quality deliverables and providing expert advice to our customers. This role requires a strong understanding of EU or US IVD Regulation, experience with assay development and (analytical &...