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Actalent
Actalent Netherlands Netherlands
2 months ago
Brand New FREELANCE Clinical Research Coordinator Opportunities!
A leading Global patient recruitment provider are working very closely with sites all across Germany. They are looking for a Freelance Clinical Research Coordinator in Leiden, Netherlands.
The Clinical Research Coordinator will have exposure working on clinical trials for their main sponsors. This is an exciting opportunity with candidates to start as soon as possible!
The Clinical Research Coordinator must have minimum 6 months clinical research experience as the CRO need an individual who can work independently as well as part of a team. Day to day responsibilities will involve a lot of patient activity and data entry within the trials on site.
All the three Freelance opportunities are well paid and flexible with hours per week.
What we are looking for is someone with the following Experience:
• 6 months minimum clinical research experience
• Experience using eCRF systems (Rave, Inform, Oracle, Red cap etc)
•... Commutable to the sites as this position will be onsite
• Ability to speak Dutch and English.
Dutch:
Gloednieuwe kansen voor FREELANCE Clinical Research Coordinator!
Een toonaangevende wereldwijde aanbieder van patiëntenwerving werkt nauw samen met locaties in heel Duitsland. Ze zijn op zoek naar een Freelance Clinical Research Coordinator in Leiden, Nederland.
De Clinical Research Coordinator zal bekendheid krijgen bij het werken aan klinische proeven voor hun hoofdsponsors. Dit is een opwindende kans met kandidaten om zo snel mogelijk te beginnen!
De Clinical Research Coordinator moet minimaal 6 maanden klinische onderzoekservaring hebben, aangezien de CRO een persoon nodig heeft die zowel zelfstandig als in teamverband kan werken. De dagelijkse verantwoordelijkheden omvatten veel patiëntactiviteit en gegevensinvoer binnen de onderzoeken ter plaatse.
Alle drie de freelance mogelijkheden zijn goed betaald en flexibel met uren per week.
Wat wij zoeken is iemand met de volgende Ervaring:
• Minimaal 6 maanden klinische onderzoekservaring
• Ervaring met het gebruik van eCRF-systemen (Rave, Inform, Oracle, Red Cap enz.)
• Pendelbaar naar de locaties, aangezien deze functie ter plaatse is
• Nederlands en Engels kunnen spreken.
Job Title: Clinical Research Coordinator
Location: Leiden, Netherlands
Job Type: Contract
Trading as Aerotek. Allegis Group Limited, Maxis 2, Western Road, Bracknell, RG12 1RT, United Kingdom. No. 2876353. Allegis Group Limited operates as an Employment Business and Employment Agency as set out in the Conduct of Employment Agencies and Employment Businesses Regulations 2003. Aerotek and Actalent Services are companies within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Actalent Services, Aston Carter, EASi, Talentis Solutions, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice available at https://www.allegisgroup.com/en-gb/privacy-notices.
To access our Online Privacy Notice, which explains what information we may collect, use, share, and store about you, and describes your rights and choices about this, please go to https://www.allegisgroup.com/en-gb/privacy-notices.
We are part of a global network of companies and as a result, the personal data you provide will be shared within Allegis Group and transferred and processed outside the UK, Switzerland and European Economic Area subject to the protections described in the Allegis Group Online Privacy Notice. We store personal data in the UK, EEA, Switzerland and the USA. If you would like to exercise your privacy rights, please visit the "Contacting Us" section of our Online Privacy Notice at https://www.allegisgroup.com/en-gb/privacy-notices for details on how to contact us. To protect your privacy and security, we may take steps to verify your identity, such as a password and user ID if there is an account associated with your request, or identifying information such as your address or date of birth, before proceeding with your request. If you are resident in the UK, EEA or Switzerland, we will process any access request you make in accordance with our commitments under the UK Data Protection Act, EU-U.S. Privacy Shield or the Swiss-U.S. Privacy Shield
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