Clinical Database Programmer
il y a 11 heures
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. The position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. This position plays a critical role on our study teams and a quality, timely database development is instrumental to the company’s success. If you are interested in an exciting career where you have the opportunity to use your knowledge and expertise and can develop and grow your career even further, then this is the position for you
Responsibilities:
- Coordinate with Data Managers to develop and maintain clinical study electronic data capture (ECR) databases according to company and/or sponsor standards;
- Perform quality checks and validation testing in collaboration with colleagues in order to deliver a quality product to our Sponsors;
- Gain and strengthen knowledge in the industry and in multiple electronic data capture systems;
- Be an active member of multiple global project teams, and collaborate across several different functional areas.
Qualifications:
- Bachelor’s degree in computer science, mathematical science, life science or related field;
- Basic level experience in at least one programming language;
- Rave and/or C# or similar programming experience preferred, but not required;
- Flexible and able to support a variety of studies;
- Meticulous attention to detail
Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?:
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
**Awards**
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
**What to Expect Next**
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
-
Experienced Clinical Database Programmer
il y a 11 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob 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...
-
Clinical Database Programmer
il y a 11 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our global business is growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team in our Leuven office. The position will work in a team to develop databases in which clinical data is captured and processed for analysis and reporting. This position plays a...
-
Clinical Data Coordinator
il y a 2 semaines
Leuven, Belgique Oliver James Associates Temps plein**We are looking for a Clinical Data Coordinator for our client in the health sector based in Leuven.** **Job description**: **Responsibilities**: - Create and manage clinical trial databases, including data entry and quality control checks - Work with clinical research staff to collect and organize study data - Generate study reports and ensure accuracy...
-
Clinical Regulatory Affairs Specialist
il y a 10 heures
Leuven, Belgique GC Europe Temps plein**GC Europe NV** is the European subsidiary of **GC Corporation**, a family-owned company with headquarters in Tokyo. It is one of the biggest suppliers of dental products with over 2300 employees all over the world and 4 production branches in Japan, the USA, China and Europe. We supply an entire range of consumer materials, equipment and facilities for...
-
Clinical Trial Manager
il y a 10 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob 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...
-
Clinical Trial Manager
il y a 10 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob 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...
-
Clinical Trial Manager
il y a 10 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob 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...
-
Clinical Trial Manager
il y a 10 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob 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...
-
Clinical Trial Manager
il y a 10 heures
Leuven, Belgique Medpace, Inc. Temps pleinJob 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...
-
Medical Writer
il y a 3 jours
Leuven, Belgique Terumo Europe Temps pleinAt Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
