A JOB AT CTS !

Medewerker CTS

For me Clinical Trial Service stands for a no-nonsense company that always thinks in possibilities instead of impossibilities. There’s a big involvement of the employees and it feels good to work with a team that is always looking for a suitable solution for every issue. Kindness, good working atmosphere, nice colleagues, straight forward and do what needs to be done are the key words for me at CTS.

 

Pauline Ophuis, Finance Department

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Medewerker CTS

Since I joined CTS as Clinical Research Associate/Project Manager in 2003,  CTS is my perfect employer. Flexible, open and dynamic in projects and mangement, warm and committed as long term colleagues, great office with designer art, reflecting the wow- factor of CTS. Continuous impulses of new developments in our business and expansion of activities are always welcome at CTS. With CTS professional enthousiasm is a way of life. In my 26 years in Clinical Research, I am committed to this company and it’s culture. For me it feels like a great match, with hopefully many more years to come.

Jolanda Schoenmakers

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Medewerker CTS

In the past year i have been working for Clinical Trial Service BV as a Research Nurse. I was involved with several clinical trial studies by visiting patients at home to perform study specific related activities. It was a great pleasure to work for and with Mirjam and her team. They are accessible, have knowledge and are motivated to achieve the best results.I can recommend anyone to work for or with Clinical Trial Service BV.

Eun Joo, Research Nurse Clinical Trial Service

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Medewerker CTS

Sinds een half jaar werk ik met veel plezier als research-verpleegkundige bij CTS. Het werk is erg afwisselend en ik waardeer de grote mate van flexibiliteit die ik krijg. CTS zorgt dat iedereen goed wordt voorbereid op projecten en is altijd bereikbaar voor overleg. Werken bij CTS betekend een interessante baan met leuke collega's, veel mogelijkheden en een betrokken team! 

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Medewerker CTS

Clinical Trial Service biedt mij een professionele werkomgeving, een comfortabele werksfeer en gezellige en ter zake kundige collega's. Het kleinschalige karakter van de organisatie, met de internationale reikwijdte zorgt voor efficiënte communicatie en bedrijfsvoering. Kortom: een werkgever naar mijn hart!
Marcel Hagmanns - Business Development

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Verpleegkundigen omgeving Gent (Belgie) gezocht.

Verpleegkundigen omgeving Gent gezocht
Wij zijn op zoek naar geregistreerde verpleegkundigen die meerdere keren per week patiënten thuis kunnen bezoeken, in de regio Gent.
Wij zoeken iemand die:
• Meerdere ochtenden (vóór 08:00 uur) per week beschikbaar is, bij voorkeur ook in het weekend;
• Ervaring heeft met subcutane injecties bij kinderen of gespecialiseerd kinderverpleegkundige is;
• Ervaring heeft met klinische studies of daar graag meer over wil weten;
• Bereid is om te reizen en in het bezit is van een auto en rijbewijs.
Vergoeding: per uur, reistijd is werktijd en kilometers worden vergoed.
Dit project is heel goed te combineren met je huidige baan.

Interesse of meer weten?
Stuur je CV en korte motivatie naar: contact@clinicaltrialservice.com Je kunt ons ook bellen: +31 53 5362220 (vraag naar Moniek Leffers of Mirjam Bruggink). We horen graag van je!

Vacancy Clinical Research Associate (CRA)

A CRA or Clinical Trial Monitor supervises medical scientific research initiated by pharmaceutical companies, medical aids companies or medical researchers. You oversee quality control with regard to the running of research and safeguarding of patient safety.

You work in a team but are also independent during visits to research centres. Your daily andweekly schedules are very dynamic, ranging from days at the office to long working days in hospital throughout the Netherlands (and sometimes Belgium).

Your work is very varied. You know the trial protocol inside out. It is important to have excellent social skills and a good spoken and written command of Dutch and English. You area good presenter and professional on the phone.

You carry out source document verification: you compare the data in the Case Report Form with the information in the patients’ medical status. You are conscientious at recording all the performed research actions. You also check whether the research is executed in accordance with the research protocol and the legislation and regulations. You take corrective measures if research workers divert from protocol and function as everyone’s go-to person.

An especially interesting and dynamic job which enables you to develop socially and scientifically. Each new trial is a new challenge, always exciting and full of surprises. It is essential that you build and maintain a valuable and long-term professional relationship with our clients, medical researchers and research workers, pharmacists and laboratory workers.

Education and experience

Have you completed a (para)medical Higher Vocational Education or University Degree, and do you have experience with medical scientific research, preferably as CRA, please apply.

Terms of employment

Clinial Trial Service BV offers excellent terms of employment and a pleasant working environment.

Interested?

Mirjam Bruggink, CEO
mirjam.bruggink@clinicaltrialservice.com
Tel: +31 53 5362220 or +31 654 281 271

Vacancy Research Nurse/Onderzoeksverpleegkundige Site Care

CTS’s Research Nurses understand that a study patient requires a slightly different approach than an ordinary patient. The patient’s safety and protection are of the utmost importance. The Research Nurses will report any side effect in accordance with the protocol’s requirements.

The Research Nurses have knowledge of the informed consent procedure in clinical studies and will inform the researcher immediately if a patient has questions or doubts about the trial. They will also no longer perform study-specific actions after a patient has withdrawn his consent.

The Research Nurses are trained in ICH-GCP. Improvements to study-specific documents will therefore be made according to ICH-GCP.

The Research Nurses perform tasks of a clinical study delegated by the researcher inaccordance with the protocol by means of Standard Operating Procedures and/or work regulations, safeguarding the quality of the collected study data. Digressions from protocolwill immediately be reported to the researcher

CTS Research Nurses can be deployed flexibly, are experienced BIG-registered nurses and have a good written and spoken command of Dutch and English. They maintain good relationships with patients and the research centre.

Our Research Nurses Site Care work in a hospital or research institute on a specific project.

Main tasks/skills (dependent on study)

-Nurse (BIG registration)
-performing study-specific tasks according to protocol
-administering drugs
-blood sampling (independently), experience with centrifugation
-Basic Life Support/ up-to- date resuscitation training
-collecting study data
-communicating with researcher and patients
-written and spoken command of Dutch and English
-willing to see patient at research institute
-preferably some experience in clinical research
-preferably trained in ICH-GCP
-available (flexibly) at short notice
-preferably in possession of a car and driving license B

Terms of employment

Clinial Trial Service BV offers excellent terms of employment and a pleasant working environment.

Interested?

Mirjam Bruggink, CEO
mirjam.bruggink@clinicaltrialservice.com
Tel: +31 53 5362220 or +31 654 281 271

Vacancy Onderzoeksverpleegkundige Home Care

CTS’s Research Nurses understand that a study patient requires a slightly different approach than an ordinary patient. The patient’s safety and protection are of the utmost importance. The Research Nurses will report any side effect in accordance with the protocol’s requirements.

The Research Nurses have knowledge of the informed consent procedure in clinical studies and will inform the researcher immediately if a patient has questions or doubts about the trial. They will also no longer perform study-specific actions after a patient has withdrawn his consent.

The Research Nurses are trained in ICH-GCP. Improvements to study-specific documents will therefore be made according to ICH-GCP.

The Research Nurses perform tasks of a clinical study delegated by the researcher inaccordance with the protocol by means of Standard Operating Procedures and/or work regulations, safeguarding the quality of the collected study data. Digressions from protocolwill immediately be reported to the researcher

CTS Research Nurses can be deployed flexibly, are experienced BIG-registered nurses and have a good written and spoken command of Dutch and English.They maintain good relationships with the researcher, Country Study managers and patients.

Our Research Nurses visit patients at home. Recruitment of patients with a rare indication or who are difficult to recruit or who have difficulty going to a research centre, can still be included in a study. CTS Research Nurses have that little bit of extra opportunity or time to level with the patient at a personal level, which may prevent premature drop-out.

Main tasks/skills (dependent on study)

-Nurse (BIG registration)
-performing study-specific tasks according to protocol
-administering drugs
-blood sampling (independently), experience with centrifugation
-Basic Life Support/ up-to- date resuscitation training
-collecting study data
-communicating with researcher and patients
-written and spoken command of Dutch and English
-willing to see patient at research institute
-preferably some experience in clinical research
-preferably trained in ICH-GCP
-available (flexibly) at short notice
-preferably in possession of a car and driving license B

Terms of employment

Clinial Trial Service BV offers excellent terms of employment and a pleasant working environment.

Interested?

Mirjam Bruggink, CEO
mirjam.bruggink@clinicaltrialservice.com
Tel: +31 53 5362220 or +31 654 281 271

Apply now !

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  • We will contact you on short notice upon receiving your application.
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