Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team. This position ...
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team. This position ...
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team. This position ...
Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory team. This position ...
Research Database Developer
Cincinnati, OH · On-site
$90K - $120K/yr
Design, develop, and maintain clinical databases and data collection systems * Implement and manage electronic data capture (EDC) systems such as Medidata Rave * Develop, design, and maintain ...
Research Database Developer
Cincinnati, OH · On-site
$90K - $120K/yr
Design, develop, and maintain clinical databases and data collection systems * Implement and manage electronic data capture (EDC) systems such as Medidata Rave * Develop, design, and maintain ...
Research Database Developer
Cincinnati, OH · Remote
$90K - $120K/yr
A thorough understanding of data integrity, secure data handling, and compliance with Good Clinical ... Develop and maintain databases using programming languages such as Visual Basic, Visual Basic for ...
Research Database Developer
Cincinnati, OH · Remote
$90K - $120K/yr
A thorough understanding of data integrity, secure data handling, and compliance with Good Clinical ... Develop and maintain databases using programming languages such as Visual Basic, Visual Basic for ...
Data Manager - Imaging
Cincinnati, OH · On-site
Coordination of data transfers with the clinical database programmers, Project Manager and external recipients; * Coordinate system development and ongoing maintenance in collaboration with the MCL ...
Data Manager - Imaging
Cincinnati, OH · On-site
Coordination of data transfers with the clinical database programmers, Project Manager and external recipients; * Coordinate system development and ongoing maintenance in collaboration with the MCL ...
Coordination of data transfers with the clinical database programmers, Project Manager andexternal recipients; * Coordinate system development and ongoing maintenance in collaboration with the ...
Coordination of data transfers with the clinical database programmers, Project Manager andexternal recipients; * Coordinate system development and ongoing maintenance in collaboration with the ...
Medpace is a full-service clinical contract research organization that provides Phase I-IV clinical ... database specifications. Responsibilities : • Write SAS programs for use in creating analysis ...
Medpace is a full-service clinical contract research organization that provides Phase I-IV clinical ... database specifications. Responsibilities : • Write SAS programs for use in creating analysis ...
Medpace is a full-service clinical contract research organization (CRO) that provides clinical ... write SAS programs, validate databases, and coordinate data management communications.
Medpace is a full-service clinical contract research organization (CRO) that provides clinical ... write SAS programs, validate databases, and coordinate data management communications.
Clinical Trial Data Program Manager
Cleveland, OH · Hybrid
$106K/yr
The Lead Clinical Trial Data Program Manager provides strategic leadership for data management operations, overseeing a team of data managers and database developers while fostering a culture of ...
Clinical Trial Data Program Manager
Cleveland, OH · Hybrid
$106K/yr
The Lead Clinical Trial Data Program Manager provides strategic leadership for data management operations, overseeing a team of data managers and database developers while fostering a culture of ...
Clinical Trial Data Program Manager
Cleveland, OH · Hybrid
$106K/yr
The Lead Clinical Trial Data Program Manager provides strategic leadership for data management operations, overseeing a team of data managers and database developers while fostering a culture of ...
Clinical Trial Data Program Manager
Cleveland, OH · Hybrid
$106K/yr
The Lead Clinical Trial Data Program Manager provides strategic leadership for data management operations, overseeing a team of data managers and database developers while fostering a culture of ...
Senior Data Engineer
$101K - $138K/yr
Basic knowledge of SQL Server databases is required; * Knowledge of C#, Azure development is a ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Senior Data Engineer
$101K - $138K/yr
Basic knowledge of SQL Server databases is required; * Knowledge of C#, Azure development is a ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Executive Director- Clinical Engineering
Cleveland, OH · On-site
$95K - $123K/yr
Word, Excel, and database skills and experience. * Working knowledge of and experience with The Joint Commission ® and other clinical engineering-related regulatory industry standards. * Ability to ...
Executive Director- Clinical Engineering
Cleveland, OH · On-site
$95K - $123K/yr
Word, Excel, and database skills and experience. * Working knowledge of and experience with The Joint Commission ® and other clinical engineering-related regulatory industry standards. * Ability to ...
Senior Data Engineer
Cincinnati, OH · On-site
$101K - $138K/yr
Basic knowledge of SQL Server databases is required; * Knowledge of C#, Azure development is a ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Senior Data Engineer
Cincinnati, OH · On-site
$101K - $138K/yr
Basic knowledge of SQL Server databases is required; * Knowledge of C#, Azure development is a ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Senior Data Engineer
$101K - $138K/yr
Basic knowledge of SQL Server databases is required; * Knowledge of C#, Azure development is a ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Senior Data Engineer
$101K - $138K/yr
Basic knowledge of SQL Server databases is required; * Knowledge of C#, Azure development is a ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Clinical Research Associate I
Westerville, OH · On-site
$25 - $27/hr
Perform day-to-day sample and database management, ensuring data accuracy, completeness, and ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Quick apply
Clinical Research Associate I
Westerville, OH · On-site
$25 - $27/hr
Perform day-to-day sample and database management, ensuring data accuracy, completeness, and ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Using SAS, program, validate and maintain mapped database * Program edit checks for external data ... We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and ...
Clinical Database Programmer information
See Ohio salary details
$75.5K is the 25th percentile. Wages below this are outliers.
$66.1K - $78.4K
33% of jobs
The median wage is $88.5K / yr.
$78.4K - $90.7K
21% of jobs
$90.7K - $103K
0% of jobs
$113.4K is the 75th percentile. Wages above this are outliers.
$103K - $115.3K
25% of jobs
$115.3K - $127.7K
1% of jobs
$127.7K - $140K
0% of jobs
$140K - $152.3K
0% of jobs
$152.3K - $164.6K
0% of jobs
$164.6K - $176.9K
3% of jobs
$176.9K - $189.2K
8% of jobs
$189.2K - $201.5K
8% of jobs
$66.1K
$113.1K
$201.5K
How much do clinical database programmer jobs pay per year?
What are the key skills and qualifications needed to thrive in the Clinical Database Programmer position, and why are they important?
To excel as a Clinical Database Programmer, you need a bachelor's degree in computer science or a related field, experience in database design, and a strong understanding of clinical data standards. Proficiency in database management systems (such as Oracle or SQL), knowledge of electronic data capture (EDC) tools like Medidata Rave, and familiarity with programming languages like SAS or SQL are commonly required, along with certifications such as CDISC or Medidata Solutions. Attention to detail, problem-solving ability, and strong communication skills are valuable soft skills for this role. Mastering these competencies is vital for ensuring high-quality, regulatory-compliant clinical trial data and effective collaboration within multidisciplinary research teams.
What is a Clinical Database Programmer job?
A Clinical Database Programmer is responsible for designing, developing, and maintaining databases used in clinical trials. They ensure that data is collected, stored, and managed efficiently while complying with regulatory standards such as CDISC and FDA guidelines. Their role involves creating database structures, writing validation checks, and supporting data analysis to ensure accurate and reliable clinical trial results. They often work with clinical data managers, biostatisticians, and regulatory teams.
What are common responsibilities and team interactions for a Clinical Database Programmer in a typical workweek?
As a Clinical Database Programmer, your primary responsibilities usually include designing, building, and validating clinical trial databases, ensuring data is collected and managed in compliance with industry standards and regulatory requirements. You will frequently collaborate with clinical data managers, biostatisticians, and study coordinators to define data collection requirements and resolve data discrepancies. Team meetings and cross-functional communication are integral parts of the role, as you work together to maintain database integrity throughout the study lifecycle. This collaborative environment provides valuable experience in both technical problem-solving and teamwork, often paving the way for advancement into senior programming or data management positions.
Other
Medical, PTO
Posted 8 days ago
Medpace rating
8.4
Based on 8 frontline employees who took The Breakroom Quiz
15th of 57 rated research
Job description
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Medpace Reference Laboratory 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 previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities- Communicate with internal teams at Medpace Reference Laboratories (MRL) regarding study progress;
- Work closely with the Project Management team to setup, validate, and maintain study databases according to sponsor specifications; and
- Programming responsibilities entail using syntax built specifically for MRL to build custom expressions that meet specific sponsor requests.
- Act as the primary data management contact for ongoing projects, which includes:
- Supplying technical support to internal Medpace personnel;
- Ensuring quality of the database build; and
- Following up on the progress of projects to ensure sponsor timeline expectations are met.
- A minimum of a bachelor's degree is required (preferably in a math, science, or informatics related field).
- Training related to the database build/programming responsibilities is provided once hired for the positions, therefore no prior programming experience is required.
- Ability to prioritize and manage multiple projects simultaneously;
- Excellent verbal and written communication skills;
- Proficient at working in a team environment;
- Strong attention to detail and accuracy; and
- Data entry and data management experience is a plus.
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 6,000 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.
Cincinnati Perks
- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
- 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.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992