Skip to content
clinitude
  • Why work at Clinitude?
  • Contact Us
Email customer support gemango Uncategorized

Clinical Research Associate – Belgium

  • September 26, 2022September 26, 2022

We are looking for Clinical Research Associate(s) to join our team in Belgium.    Supporting the clinical research by selecting the right sites to participate in clinical study, performing initiation visits and monitoring visits to ensure good quality of data and managing the site study team are the key ingredients for this role.  Are you interested to contribute to science, we just ask you to send us your CV and start your CRA carreer.

Your Responsibilities:

  • Perform site selection if applicable, initiation, monitoring and close out visits in accordance with contracted scope of work and good clinical practice.
  • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
  • Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, CRF completion and submission, and data query generation and resolution. May support start-up phase.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Build awareness of features and opportunities of the study site.
  • Collaborate and liaise with study team members for project execution support as appropriate.
  • If applicable can be involved in the review of monitoring documents (e.g. monitoring plan, review of monitoring visit reports….).
  • To implement a quality management plan
  • To ensure timely resolutions for compliance issues

What do we ask from you?

  • basic knowledge of clinical research
  • strong written and verbal communication skills
  • strong organizational and problem-solving skills
  • effective time management
  • ability to establish and maintain effective working relationships with colleagues, managers and clients
  • degree in health care or scientific discipline or equivalent
  • 1 year on site monitoring is a plus, but not a requirement

 

If you are interested, please send us your CV and motivation and get in touch with us at hr@clinitude.com

Uncategorized

Clinical Data Management Lead (CDM Lead)

  • February 5, 2022September 29, 2022

At Clinitude we are looking for a CDM Lead for our office in Cebu, the Philippines.  The CDM Lead at Clinitude manages the end-to-end delivery of services related to data management for several projects.  The CDM Lead will need ensure quality deliverables on time and within budget and to customer satisfaction.  The CDM Lead provides leadership and vision to the team in the areas of project planning, execution and close out.  The CDM Lead will need to comply with Good Clinical Practices (GCP), ISO14155, applicable regulatory guidelines, SOPs, policies and where applicable, CDM guidance documents.

Read more “Clinical Data Management Lead (CDM Lead)” →

Posts navigation

1 2

We Are Looking For..

  • CRA/ Site Support Liaison – Cebu
    October 3, 2022
    Clinitude is a sister company of Gemango Software Read More
  • C# .Net Developer
    September 29, 2022
    We are starting new exciting projects and are looking to expand our current team of .Net Software Engineers. Read More
  • Great unwinding at Kalanggaman Island!Clinical Systems Coordinator – Belgium
    September 26, 2022
    The Clinical Systems Coordinator is responsible for Read More
  • Clinitude happyClinical Data Associate (CDA) – Cebu
    September 26, 2022
    A CDA is accountable for proper capturing, recording, Read More
  • clinitude craClinical Research Associate Liaison (CRA LIAISON) – Cebu
    September 26, 2022
    Have you always been interested in how new drugs/devices are being developed, tested and registered? Clinitude, a long time partner of Gemango is looking to welcome you to become a part of the Cebu CRA team!Read More

Here in Clinitude…

We Work..

Our Belgian office starts its day at 9 AM and our Cebu office starts its day at 2PM, Mondays to Fridays

We Dress..

Business Casual

We Speak..

English

Our Benefits..

  • Personal growth possibilities
  • Above-Industry leave and travel benefits

A Sneak Peak at Clinitude..

Clinitude Valentine's Day 2020!
Valentine’s Day 2020! <3

We Are Located…

Europe Office

Belgium

Alfons Smetsplein 3H1

3000 Leuven

+32 16 58 19 84

US Office

Chicago

10 South Riverside Plaza

Suite 875, Chicago

Illinois, 60606

+1(0) 312 474 6080

Asia Offices

The Philippines

IT Tower 1, Rm. 14B

Ayala Business Park,

6000 Cebu

Empty This

Singapore

8 Marina View,

#43-01 Asia Square, Tower 1,

Singapore, 018960

+65 6407 1163

© Clinitude 2008-2020. All Rights Reserved. Powered by Gemango Software Services Inc.

Follow us on

  • Twitter
  • Facebook
  • LinkedIn