This job has expired

Clinical Data Manager OR Senior Clinical Data Manager - P

Start date
29 Oct 2022
Closing date
27 Nov 2022

View more

You need to sign in or create an account to save a job.

Job Details

Location: Belgium - Home Based or Office Based in Brussels

Schedule: Full-time, permanent

CROMSOURCE is a growing international CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Clinical Data Manager II or Senior Clinical Data Manager. The Data Manager will be responsible for controlling, coordinating and performing data management tasks for their assigned projects in order to deliver high quality data for statistical analysis.

Join our team and help us deliver clinical trials that will improve patients' lives.

Main Job Tasks and Responsibilities:
  • Performs data management project duties, such as project set-up, project planning, project review and reporting, project administration, project co-ordination and mentoring, to ensure appropriate quality of data management deliverables within agreed timelines
  • Supervises or performs the creation of the mock CRF
  • Creates the data validation plan and interacts with the eCRF designer during the UAT of the eCRF screens and data validation routines in the EDC environment
  • Is responsible for creation, maintenance and locking/unlocking of the clinical trial database ensuring high-quality data processing
  • Operates all in-house data management processes, including in-house review, data coding, discrepancy management, data validation in clinical trials and clinical investigations
  • Performs communication with (internal and external) clients to guarantee sufficient exchange of relevant information and to maintain good client relationship
  • Liaises with the clinical project manager, medical writer, statistician, computer specialists and monitors to ensure optimal data processing

Education and Experience:
  • Higher education in sciences, medical or paramedical degree, medical information specialist or other equivalent scientific training
  • Excellent knowledge of Data Management workflow and the relevant guidelines for the conduction of clinical trials (e.g. ICH-GCP)
  • Excellent knowledge of clinical trials and clinical investigations
  • Proven practical experience in data management within the conduct of all stages of a clinical trials and clinical investigations
  • Good knowledge of EDC tools in the setup, conduct and closure of clinical studies and clinical investigations
  • Good knowledge of English and local language
  • Good communication skills, team player attitude

Our Benefits:
  • Competitive salary
  • Group and hospitilisation insurance
  • Electronic meal vouchers
  • Internet reimbursement
  • Excellent work-life balance
  • Full performance and development process with end of year reviews
  • Team events and end of year party
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally
  • Employee satisfaction survey - your feedback is important for continuous improvement

The Application Process

Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step.

If you would like to discuss the role before applying through the website @ please contact for more information.

Who will you be working for?


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.

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 Data Manager, Data Management, DM, CDM, Contract Research Organisation, CRO, Permanent
Skills: Clinical Data Manager, Clinical Data Management Location: Belgium Share:

LinkedIn Facebook Twitter Email


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.

Find Us
+44 (0) 1786 468990
6-9 The Square
Stockley Park
UB11 1FW
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert