Clinical Trial Assistant, Netherlands - L

Employer
CROMSOURCE
Location
Netherlands
Salary
Competitive
Closing date
24 Sep 2020

View more

Discipline
Clinical Research, Clinical Trials Manager / Administrator
Hours
Full Time
Contract Type
Permanent
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Description:
TalentSource Life Sciences is currently searching for an experienced Clinical Trial Assistant

to join one of our partner companies, a large pharmaceutical company involved in a wide range of therapeutic areas, in Amsterdam, the Netherlands.

The Clinical Trial Assistant (CTA) works within the Clinical Operations team and is responsible for adequate administrative, logistic and operational support to clinical trials from start-up until completion, within defined time lines and in accordance with ICH-GCP and/or other ethical and regulatory requirements and Company procedural documents.

As a CTA you are of course passionate about clinical trials. You manage your work independently, but at the same time you work in collaboration with trial team members on one or several and clinical trials.

The trial team will come to you as you are the reference for the local trial master file.

Main Responsibilities:
  • Responsible for collecting, checking and archiving all essential documents within the study according to GCP guidelines
  • Compile and update the Investigator File and Trial Master File, in collaboration with the CRA (Clinical Research Associate) and CSM (Clinical Study Manager)
  • Enter and upload study data in the various computer systems
  • Planning and taking minutes during study meetings
  • Collecting / requesting, checking and processing various data
  • Enforcement of rules according to SOPs and study milestones


Education and Experience:
  • MBO + working and thinking level
  • Minimum 1 year experience


Experience and Skills:
  • Computer expert and skilled
  • Good expression skills
  • Being able to work independently as well as in a team
  • Preferably knowledge of medical terminology
  • English and Dutch, both orally and in writing
  • Collaboration within the local study team
  • Customer friendliness and satisfaction (internal / external)
  • Flexibility
  • Stress resistance
  • Proactivity
  • Accuracy
  • Project work


Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/job-information/?job-id=HQ00002314

or please contact Alexander.Sourounis@cromsource.com for more information.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Key words: Clinical Trial Assistant
Skills: Clinical Trial Assistant, Administration, eTMF, GCP, MS Office, TMF Location: Netherlands Share:

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CROMSOURCE is an ISO-certified international provider of fully outsourced services to the pharmaceutical, biotechnology and medical device industries, specialised in clinical development and flexible resourcing solutions. CROMSOURCE was founded in 1997 and its successful growth has been built on stability, integrity, and high levels of customer satisfaction. We have grown steadily through offices across all regions of Europe and North America and delivering a comprehensive breadth of services.

Acting through PharmaceuticalMedical Device and Flexible Resourcing Solutions teams, and with a comprehensive portfolio of services, we offer a flexible approach to ensure CROMSOURCE optimally supports the unique needs of each client. This could mean providing regulatory consultancy to a small company at the early stages of a medical device development programme, through to provision of full services to a pharmaceutical company performing an international mega-trial to support registration of their product. Whatever the size and scope of the project, each receives the same level of attention to detail and commitment to delivery of a high quality service within budget and to timelines agreed.

We are experts providing experts and we live by our motto – Advise Agree Deliver. This means we leverage our experience and expertise at the early stages of discussions with our clients to freely advise them on the optimal project plan. We then reach agreement with each client on the scope of service, timelines and budget. CROMSOURCE then commit to deliver those services on time and within budget – according to our End-to-End Guarantee and this commitment to guaranteed delivery is unique in the clinical research environment.

Contact Us
  • 6-9 The Square
  • Stockley Park
  • Hayes
  • UB11 1FW
  • United Kingdom
  • +44 (0) 1786 468990
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