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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Project Manager International home care service

Clinical Trial Service BV is een contract research organisatie gespecialiseerd in het opzetten en uitvoeren van medisch-wetenschappelijk onderzoek (clinical trials) in Europa en daarbuiten.

Vanwege een significante groei van ons bedrijf gaan wij het project managers team van de internationale home care service uitbreiden. Daarom zijn wij op zoek naar een Project Manager die internationale projecten coördineert. 

Wij zoeken een project manager die:

  • Bij voorkeur verpleegkundige is of een paramedische opleiding op HBO/WO niveau heeft afgerond;
  • Inzetbaar is op korte termijn;
  • Een baan zoekt voor 0.8-1.0 FTE
  • Ervaring heeft met klinische studies;
  • Woonachtig is in de regio Enschede;
  • De Engelse taal machtig is in woord en geschrift;
  • Goed communiceert;
  • Een goede organisator is;
  • Sociaal vaardig en collegiaal is.

Vergoeding: salaris in overleg.

Clinical Trial Service BV is een uniek bedrijf dat al 27 jaar medisch wetenschappelijk onderzoek uitvoert. We hebben goede arbeidsvoorwaarden en een bijzonder leuke en goede werksfeer. Kijk op onze website voor meer informatie:

www.clinicaltrialservice.com

Interesse of meer weten?
Stuur je CV en korte motivatie naar: mirjam.bruggink@clinicaltrialservice.com Je kunt ons ook bellen: 053 5362220 (vraag naar Mirjam Bruggink) of 0654281271

We horen graag van je!

Wij zien jouw sollicitatie graag tegemoet.

Hartelijke groet,

Het team van Clinical Trial Service BV

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

Vacancy Ervaren Research Verpleegkundige in Groningen (Fulltime)

Clinical Trial Service B.V. is op zoek naar een ervaren research verpleegkundige, bekend met het uitvoeren van medisch-wetenschappelijk onderzoek (clinical trials) en goede kennis van wet- en regelgeving waaronder Good Clinical Practice.

Start: maart / april 2020
Periode: 1 jaar – mogelijk verlenging van 1 of 2 jaar
Locatie: UMCG

De taken zullen bestaan uit het plannen en uitvoeren van de patiënten bezoeken, het invoeren van data in het (e)CRF, het bijhouden van formulieren, administratie en Investigators Site File. Er wordt verwacht dat je goed communiceert met het studie team, dat je een pro-actieve en initiatiefrijke teamplayer bent.

Wij zoeken een ervaren research verpleegkundige die:
– Bij voorkeur ICH-GCP getraind is
– Venapunctie kan uitvoeren
– (e)CRFs kan invullen
– Over goede communicatie eigenschappen beschikt
– Flexibel, meedenkend en initiatief-rijk is

Wij bieden goede werkomstandigheden en een goed salaris.

Ben jij op zoek naar een leuke research baan, voldoe je aan het profiel en ben je full time beschikbaar, stuur dan een motivatie brief en CV met een uitgebreide beschrijving van jouw werkervaring naar onderstaand email adres. Als meer wilt weten over de functie mail of bel ons dan met jouw vragen.

Clinical Trial Service BV
Marieke Bons, Manager Home Care Service
marieke.bons@clinicaltrialservice.com
Tel: 0654244210 of 0535362220
Bereikbaar op maandag, dinsdag, donderdag en vrijdag

Clinical Trial Service BV is een Contract Research Organisatie, sinds 1993, gespecialiseerd in internationale home care service voor clinical trials, het detacheren van research verpleegkundigen voor clinical trials in ziekenhuizen en onderzoeksinstellingen en voert project management en monitoring uit.

Op onze website tref je uitgebreide informatie over Clinical Trial Service BV: www.clinicaltrialservice.com

Apply now !

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