Vacatures Regulatory assistant Nederland

35 vacatures

Regulatory Consultant - IQVIA MedTech (EU, Home-based)

 ...Overview Under general supervision, Prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization...  ...porcedures consistently; provides independent thought to assist in process improvements; • Ability to make decisions on... 

IQVIA

Nederland
10 dagen geleden

Regulatory Affairs Manager

 ...expertise. This role is a great opportunity for an experienced regulatory professional with broad regulatory experience and expertise to...  ...feedback on the quality of technical documents, and may assist in their training and development; • May present to clients at... 

IQVIA

Nederland
26 dagen geleden

Regulatory Affairs Manager - Clinical trials

 ...several years of experience in the professional discipline, works independently under limited supervision. Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.... 

IQVIA

Nederland
5 dagen geleden

Regulatory Senior Manager - EU Chemical Policy

 ...around the world. The successful candidate will have responsibility to oversee Chemours’ chemical policy work. The Senior Regulatory Manager – EU Chemical Policy will ensure the development and execution of proactive advocacy strategies to advance Chemours’ and... 

Chemours

Nederland
28 dagen geleden

Médecins du Monde international network coordinator

 ...v Supervise budget expenditure and approve all financial transactions in collaboration with the Financial Coordinator and Network Assistant v Prepare the annual budget in accordance with annual workplans v Prepare final financial reports Qualifications The ideal... 

MDM

Nederland
11 dagen geleden

Associate Director - Center for Statistics in Drug Development

 ...on state-of-the art design approaches and analysis methods, and assist with data displays and interpretations of data analysis results...  ...design strongly preferred Must have some knowledge of regulatory bodies and compliance within the pharmaceutical and CRO space.... 

IQVIA

Nederland
3 dagen geleden

Quality Assurance Auditor

 ...assigned by QA management: External Audits Management: Assist with preparation and hosting of Sponsor audits of ICON and of Investigational...  ...or Pharma ~2+ years experience working the clinical, regulatory, or quality environment within CRO/ pharmaceutical / healthcare... 

ICON

Nederland
10 dagen geleden

Clinical Research Associate

 ...services as well as vendors You will communicate with internal project teams regarding the progress of the study Support the regulatory team in preparing documents for submissions CRA Requirements: Degree within Life Sciences or something relevant... 

AL2S3 LTD

Nederland
6 dagen geleden

Director, Real-World Evidence Oncology (Post Authorization Studies)

 ...including development of study reports and pertinent sections of regulatory documents, publications, white papers, press releases, etc....  ..., returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory... 

Gilead Sciences

Nederland
11 dagen geleden

Research Pharmacokinetics Director

 ...clinical development plans, and dossiers for product registration. Assist Clinical Pharmacology management in implementing strategic...  ...dossiers for product registration and communicate with local regulatory agencies Ensure quality and timely delivery of the project PK... 

IQVIA

Nederland
3 dagen geleden

Senior Medical Writer - Oncology

 ...succeed and a passion that ensures what we do, we do well. What will you be doing? Researches, writes, and edits clinical and regulatory documents by applying functional expertise and clinical drug development knowledge. Writes clear and concise documents, including... 

ICON

Nederland
29 dagen geleden

Medical Director Oncology/Hematology

 ...you meet the Knowledge, skill, and education requirements for the role? Robust and current knowledge of scientific, clinical, regulatory, commercial, and competitive landscape within Oncology solid Tumour (Essential) Clinical background in Radiotherapy as a board-... 

IQVIA

Nederland
25 dagen geleden

Principal statistician

 ...Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics. Keywords Biostatistician / statistician / stats / CRO / Pharma... 

i-Pharm Consulting

Nederland
12 dagen geleden

Manager, Biostatistics - Global BIOS (Home-Based/Hybrid: UK/Europe)

 ...most complex statistical methods that apply to Phase I-IV clinical trials In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with... 

IQVIA

Nederland
6 dagen geleden

Study Start Up Manager - (Home based, UK/EU) - IQVIA Biotech (Evergreen)

 ...activities for projects or programs. This includes the overall management and oversight of the following processes: site feasibility, regulatory approval, and site contracts. They may be assigned to manage the site start-up activities for a country, region, or entire... 

IQVIA

Nederland
4 dagen geleden

Sr. Product Manager

 ...keeping mission-critical workloads highly available, protecting data everywhere, and providing insights to optimize costs and maintain regulatory readiness. Veritas supports 500+ data sources, 150+ storage targets, 50+ clouds, and any deployment model imaginable. We... 
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Veritas

Nederland
27 dagen geleden