10 beste vacatures voor de functie van clinical research in brussel hoofdstad (nieuwe medewerkers gezocht)

Clinical Research Associate - French Speaking - Any EMEA location
North American Science Associates Ltd. —Brussel-Hoofdstad
- Onderzoek
- Master
- Organisatorische vaardigheden
Snel solliciteren
3 dagen
Health Economic and Outcomes Research Manager M/F/D
MSD —Brussel
- Voltijds
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- Doctoraat
- Onderzoek
Medical Development Program - Physician (New to Industry)
UCB —Anderlecht
- Onderzoek
9 dagen
Medicine Specialist (Fluent in French) - Freelance AI Trainer Project
Meridial —Brussel
- € 8 - € 65 per uur
- Thuiswerk
- Geneeskunde
- Doctoraat
- Master
(Associate) Medical Director - Neurology
Thermo Fisher Scientific —Brussel
- Voltijds
- Bachelor
4 dagen
Project and Services Assistant
EORTC —Brussel
- Voltijds
- Microsoft Excel
- Microsoft Outlook
- Onderzoek
9 dagen
Data Science Lead
UCB —Anderlecht
- Geneeskunde
- Doctoraat
- Master
Medical Advisor Opthalmology /New Products (M/F/D)
MSD —Brussel
- Voltijds
- Doctoraat
- Verkoopervaring
- Onderzoek
9 dagen
Clinical fellow - microbiologie
UZ Brussel —Jette
- Voltijds
- Geneeskunde
- Onderzoek
- Master
- Reiskosten vergoeding
- Openbaar vervoer vergoeding
Clinical Trial Supply Manager – Brussels, Belgium (F/M)
Sotec Consulting —Brussel
- Voltijds
- Master
- Managementervaring
- Communicatieve vaardigheden

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Clinical Research Associate - French Speaking - Any EMEA location

North American Science Associates Ltd. -
Brussel-Hoofdstad

Snel solliciteren

Vacaturegegevens

3 dagen geleden

Kwalificaties

Frans
Onderzoek
Master
Organisatorische vaardigheden
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

Verfijn je zoekopdracht

clinical research vacatures in brussel hoofdstad

Clinical Research Associate - French Speaking - Any EMEA location

Health Economic and Outcomes Research Manager M/F/D

Medical Development Program - Physician (New to Industry)

Medicine Specialist (Fluent in French) - Freelance AI Trainer Project

(Associate) Medical Director - Neurology

Project and Services Assistant

Data Science Lead

Medical Advisor Opthalmology /New Products (M/F/D)

Clinical fellow - microbiologie

Clinical Trial Supply Manager – Brussels, Belgium (F/M)

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van clinical research in brussel hoofdstad

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