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Vacatures in de zorg

0-15 (totaal 2611 vacatures gevonden)

  • Omschrijving vacature
    Toelichting
  • Verzorgende IG (part-time vaste baan)

    Ben je als Verzorgende IG op zoek naar vaste uren en woonachtig in de omgeving van de Utrechtse Heuvelrug? Dan komen wij graag met je in contact!

    Als verzorgende IG ben je verantwoordelijk voor het welzijn en de zorg van de cliënten vanuit een zelfsturend team. Met als doel dat mensen zolang mogelijk thuis kunnen blijven wonen. Dit betekent dat je naast het leveren van zorg als team ook verantwoordelijk bent voor de coördinatie van de zorg. Zoals het voeren van intake-gesprekken met nieuwe cliënten, het aanvragen van indicaties en het onderhouden van zorggerelateerde contacten rondom de cliënt. Je deelt samen het werkrooster in en hebt een begeleidende rol voor stagiaires en collega's.
     

    Plaats: Utrechtse Heuvelrug
    Naam: Daan BV
  • Project Specialist I

    job ID: 16330

    Position Title: Project Specialist I

    Working Location: Europe - Any INC Office

    Employment Status: Full-Time

    Required Experience: Not Applicable

    Required Education: Not Indicated

    Required Travel: 0

    Job Summary:
    Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we’ve continued to improve what we do.

    We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with INC Research’s Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research.

    We are currently looking to strengthen our Project Management team and are seeking Project Specialist I to our Oncology Business Unit to be based in the United Kingdom or in the Netherlands.
    Core Responsibilities:
    A brief summary of duties you will be involved in:

    • Project Administration - Attends Quick Start camp, Quality Finish Camp, and may attend process review and Kick-Off Meetings and other project meetings as required.
    • Reporting - Assists project team with compliance or maintenance of regulatory standards, Standard Operating Procedures (SOPs), and Work Instructions (WI). Reviews and submits Essential Regulatory Documents for second review
    • Communication - maintains timely and effective communication among team members and site staff. Keeps Project Leadership and Clinical Research Associates (CRAs) fully appraised of sites and study status
    • Training - May train new employees assigned to project

    Skills & Attributes:
    To succeed in this role you will need the following skills/experience:

    • BA/BS in the science/healthcare field, nursing degree, or equivalent combination of education and experience
    • Minimal clinical research experience
    • Basic understanding of the drug development process.
    • Exceptional attention to detail, organizational, interpersonal, and communication skills with demonstration of critical thinking and problem solving skills; ability to perform several tasks simultaneously to meet deadlines
    Why choose us:
    It takes skill and passion to develop medicines the way we do. Don’t worry – if you’ve got the passion part, we’ll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
    We’ve got an attitude at INC: “Can do, I own it.” Absolutely everyone has ownership of what they do here. And because we’re given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
    “We were ranked “Top CRO” to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide).”
    What happens next:
    If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity .
    Plaats: Any INC Office, GB-SRY
    Naam: StepStone
  • CRA III (Netherlands)

    Description

    Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we’ve continued to improve what we do.

    At INC Research, we understand the nuances that differentiate post-approval studies from pre-approval trials – nuances that are critical to consider as early as possible during development to ensure your products reach their full potential.
    Our Post-Approval team is a dedicated clinical operations team with tools and study implementation procedures specifically created for late phase research.
    We are currently looking to strengthen our Clinical Monitoring team in The Nethelands and are seeking CRA III for our Post Approval and Cardiovascular Business Unit to be based in our Amsterdam office. We can also accept home office based workers too.
    Core responsibilities:
    A brief summary of duties you will be involved in:
    ·Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
    ·Data Handling, Reporting, Tracking and administrative tasks
    ·Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.

    Qualifications

    Skills and attributes:

    To succeed in this role you will need the following skills/experience:

    . Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position

    · Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
    · Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines
    · Good command of written and spoken English language
    Why choose us:
    It takes skill and passion to develop medicines the way we do. Don’t worry – if you’ve got the passion part, we’ll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
    We’ve got an attitude at INC: “Can do, I own it.” Absolutely everyone has ownership of what they do here. And because we’re given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
    “We were ranked “Top CRO” to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide).”
    What happens next:
    If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.
    Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract.

    Occasionally required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
    Plaats: Nederland
    Naam: StepStone
  • Clinical Research Associate II - Oncology

    Description

    Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we’ve continued to improve what we do.

    We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with INC Research’s Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research.

    We are currently looking to strengthen our Clinical Monitoring team in the Netherlands and are seeking a CRA II for our Oncology Business Unit.

    A brief summary of duties you will be involved in:

    • Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures

    • Data Handling, Reporting, Tracking and administrative tasks

    • Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines

    Qualifications

    To succeed in this role you will need the following skills/experience:

    • Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position

    • Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO

    • Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines

    • Good command of written and spoken English language

    Why choose us:

    It takes skill and passion to develop medicines the way we do. Don’t worry – if you’ve got the passion part, we’ll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.

    We’ve got an attitude at INC: “Can do, I own it.” Absolutely everyone has ownership of what they do here. And because we’re given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.

    “We were ranked “Top CRO” to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide).”

    What happens next:

    If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.

    Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract.


    Occasionally required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
    Plaats: Amsterdam
    Naam: StepStone
  • Clinical Team Leader

    Description

    Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we’ve continued to improve what we do.

    We are currently looking to strengthen our Clinical Monitoring team and are seeking a Clinical Team Leader who can be office or home based in Western Europe.
    A brief summary of duties you will be involved in as a CTL:
    · Attends Kick-Off, Quick Start, and Investigator meetings.
    · Develops clinical plans and guidelines, including clinical monitoring plans.
    · Assures compliance with monitoring intervals according to the project requirements.
    · Responsible for site assignments for CRAs and reviews site visit reports.
    Qualifications

    To succeed in this role you will need the following skills/experience:

    · Degree educated in the science/health care field or nursing degree, or equivalent
    · Lead CRA experience which includes leading CRA's throughout Europe.
    Why choose us:
    It takes skill and passion to develop medicines the way we do. Don’t worry – if you’ve got the passion part, we’ll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
    We’ve got an attitude at INC: “Can do, I own it.” Absolutely everyone has ownership of what they do here. And because we’re given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
    “We were ranked “Top CRO” to work with in the CenterWatch 2013 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide).”
    What happens next:
    If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.
    Plaats: Madrid
    Naam: StepStone
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