Experienced Clinical Research Associate

**Clinical Research Associate BE**: **Location** - Leuven, Belgium **Contact name** - Sophie Krakers **Job ref** - 20725 **Published** - 7 months ago **Looking for a CRA in Belgium** For our partner, an organically growing CRO, we are looking for a Clinical Research Associate. This CRO provides phase I-IV clinical development services to the...

reMYND is a clinical stage company developing treatments for Alzheimer’s, Huntington's, epilepsy and other diseases caused by cellular dysfunction. reMYND’s most advanced program is ReS19-T, an investigational compound for the treatment of Alzheimer’s, ready to start Phase 2a. **Open Position: Research Associate** **Your role**: Supporting the...

reMYND is a clinical stage company developing treatments for Alzheimer’s, Huntington's, epilepsy and other diseases caused by cellular dysfunction. reMYND’s most advanced program is ReS19-T, an investigational compound for the treatment of Alzheimer’s, ready to start Phase 2a. **Open Position: Research Associate** **Your role**: Supporting the...

Starting date: ASAP Type of contract: Permanent Location: Leuven, BELGIUM Job offer: Research associate in Chemistry (M/F) - Leuven (BELGIUM) Job description Under the responsibility of a chemical NovAliX Project Manager, you will join a clinical-stage start-up in which you will contribute by molecule syntheses to move forward the research programs on...

**Position**:Research Associate in Chemistry (M/F) **Starting date**:ASAP **Type of contract**:Permanent contract **Location**:Leuven Area, Belgium **Job description**: Under the responsibility of a chemical NovAliX Project Manager, you will join a clinical-stage start-up in which you will contribute by molecule syntheses to move forward the research...

Job Summary: Our global business is growing rapidly, and we are currently seeking a full-time office-based Clinical Database Programmer to join our Data Management team in our Leuven office. This position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. The role requires the ability to...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, Leuven. Clinical Trial Managers with expertise in Oncology/Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to...

Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office/home-based** Experienced Clinical Database Programmer** to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...

Experienced Clinical Database Programmer My Client who is a very successful, mid-size CRO are currently looking for an Experienced Clinical Database Programmer to join their team on a Hybrid bases in one of three locations; Leuven(Belgium), Milan(Italy) or Rotterdam(Netherlands). They are constantly growing, which allows for your personal growth as well as...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Leuven, Belgium. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or to expand to a new therapeutic area....

Company Description PSI is a leading full-service global Contract Research Organization providing a wide range of clinical trial services to the pharmaceutical and biotechnology industry, mainly for the development of clinical drugs. PSI has 2,300+ employees and 40+ affiliates in Europe, North and South America, Asia Pacific and South Africa. Job...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, particularly in our Leuven office. Clinical Trial Managers with expertise in Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, particularly in our Leuven office. Clinical Trial Managers with expertise in Oncology/Hematology are welcome to continue to work in their area of expertise or to...

Description: **Location**: Leuven, Belgium - hybrid **Schedule**: Freelance - 0.2 FTE Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds. TalentSource Life Sciences (the sponsor-dedicated...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, particularly in our Leuven office. Clinical Trial Managers with expertise in Infectious Disease are welcome to continue to work in their area of expertise or to...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, particularly in our Leuven office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Belgium, particularly in our Leuven office. Clinical Trial Managers with expertise in Immunology/GI are welcome to continue to work in their area of expertise or to expand...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

Clinical Data Coordinator | Full-time | CDI | English | Leuven | 1094059 Hays is looking for a Clinical Data Coordinator (CRO) to join our client data management team. **Your responsibilities as a Clinical Data Coordinator (CRO)** In this role, you will have the opportunity to put your analytical skills to use by validating database designs, reporting on...

Our client, a multinational Clinical Research Organization, is currently looking to hire an Account Analyst to join their Finance and Accounting team in Leuven, Belgium. It is a permanent role for a professional who would be responsible for budget oversight for clinical trials and support for various departments throughout the organization. This would...