Clinical Database Programmer - Entry Level

at  Medpace Inc

3001 Leuven, Vlaams-Brabant, Belgium -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate16 Dec, 2024Not Specified17 Sep, 2024N/ALife Science,Computer ScienceNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

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.

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


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Computer science mathematical science life science or related field

Proficient

1

3001 Leuven, Belgium