20 beste vacatures voor de functie van computer vision in de kennemerduinen (nieuwe medewerkers gezocht)

Clinical Research Associate - French Speaking - Any EMEA location
North American Science Associates Ltd. —Amsterdam Centrum
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3 dagen
Senior AI Tech Consultant / Manager (ERP/SAP) - Amsterdam | BCG Platinion
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Principal Data Engineer - Data & AI, Marketplace
Booking.com —Amsterdam Centrum
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- Java
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Senior Art Director – Fashion
INDG —Amsterdam
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Construction Robot Operator, UK
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Senior Technology Consultant (CPG)
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Kids II Inc —Amsterdam
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Airwallex —Amsterdam
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- Salesforce
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Ik wil de nieuwste vacature-alerts ontvangen voor de functie van computer vision in de kennemerduinen

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Clinical Research Associate - French Speaking - Any EMEA location

North American Science Associates Ltd. -
Amsterdam Centrum

Snel solliciteren

Vacaturegegevens

Kwalificaties

Frans
Engels
Onderzoek
Organisatorische vaardigheden
Klinische studies
Computervaardigheden
Communicatieve vaardigheden

Volledige vacaturetekst

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core

Values:

Act with integrity in everything we do.
Provide best-in-class customer experiences.
Develop superior talent and deliver expertise.
Respond with agility and provide timely results.
Embrace collaboration, diverse perspectives and ideas.

Job Description:

Works on assigned studies to ensure that human subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations are followed.
Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicable regulatory guidelines.
May conduct on-site and remote site qualification, site initiation, interim, and site close-out monitoring visits.
Serve as primary point of contact for site questions relating to study enrollment, conduct, and close-out issues: liaise with appropriate study team members as needed.
Communicates through verbal and written communication with site investigator and project team overall site performance, trends, deficiencies, and concerns.
Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc.
Performs study-related training.
Manages the development and maintenance of study documents, processes and systems as assigned.
Ensures quality and completeness of central and site master files. Tracks and maintains required study documents, performs quality control review, manages renewals.
Tracks study site and over all study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance.
Attends internal and external meetings as required.
Provides all job-related progress reports and visit documentation as required.
May support safety activities such as narrative writing, managing the CEC/DSMB, etc.
OUS: Prepares and coordinates submissions to regulatory authorities.
May perform other activities as assigned.

Must be fluent in French residing in one of the NAMSA locations noted above preference is the UK given our client portfolio. This role is external/field based CRA work which will align with the higher travel percentage.

Qualifications & Technical Competencies:

Must be fluent in French residing in one of the locations noted above preference is the UK given our client portfolio. This role is external/field based CRA work which will align with the higher travel percentage.

Work portfolio is a required 8-9 visits per month aligned with 6-8 protocols across approximately 20 sites.

Fluency in English and local language, if different, required.
Higher education degree or equivalent education, training, and experience.
Preferred 2 years clinical trial experience or medical device.
Required 3-5 years monitoring experience.
Able to work independently once trained.
Good verbal and written communication skills.
Strong organizational skills.
Basic computer proficiency.
Understanding of clinical research processes and regulations.
Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required

Snel solliciteren

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computer vision vacatures in de kennemerduinen

Clinical Research Associate - French Speaking - Any EMEA location

AI Solutions Consultant - Amsterdam | BCG Platinion

Senior Data Scientist (ML & Statistical Modelling)

eCommerce Analytics Manager (Measurement Strategy & Customer Analytics)

Intern/Associate Consultant Data Science

Technical Support Engineer

Senior AI Tech Consultant / Manager (ERP/SAP) - Amsterdam | BCG Platinion

Principal Data Engineer - Data & AI, Marketplace

Senior Deep Learning Research Engineer

Software Engineer, Autonomy/Robotics

Junior Product Manager - Smartphones

Senior Art Director – Fashion

Construction Robot Operator, UK

Product Manager - Consumer App

Senior Technology Consultant (CPG)

Associate Category & Product Manager

Senior Applied Scientist

Account Executive - SaaS IA - Benelux

Software Engineer, Search Experience

Staff Product Manager, GTPN

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van computer vision in de kennemerduinen

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