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Medical Computer Engineer jobs
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- Medpace, Inc.London EC4V 3BJ
- Bachelor’s degree in computer science, mathematical science, life science or related field;
- Medpace is a full-service clinical contract research organization (…
- View all Medpace, Inc. jobs - London jobs - Programmer jobs in London
- Salary Search: Clinical Database Programmer salaries in London
- See popular questions & answers about Medpace, Inc.
- Computer FuturesLondon
- Ensure compliance with relevant medical device standards and regulatory requirements.
- Knowledge of standards such as ISO 14971, IEC 62304, and related medical…
View similar jobs with this employerSThreeBirmingham- Additional certifications in quality management or medical device compliance.
- Experience with Class III medical device validation, testing or quality assurance.
- Working knowledge of ISO 13485 (medical device quality management) and IEC 62304 (medical device software lifecycle).
- Domain: Class III medical device · system validation.
- Professional development in medical device compliance and validation methodologies.
View similar jobs with this employerelix sourcing solutionsMaidstone- Following continued investment and expansion, the business is looking to add a Systems Engineer to support multidisciplinary projects across the full…
View similar jobs with this employerelix sourcing solutionsMaidstone- Following continued investment and expansion, the business is looking to add a Systems Engineer to support multidisciplinary projects across the full…
- SartoriusRoyston
- Annual leave
- Free parking
- Private dental insurance
- Company pension
- Private medical insurance
- Work from home
- In this role, you will develop electronic and firmware solutions, applying them in innovative ways to enable new products and deliver continuous improvements to…
View similar jobs with this employerSThreeBirmingham- Domain: Class III medical device · ISO 13485 · IEC 62304.
- Working knowledge of ISO 13485, IEC 62304 and Class III medical device validation.
Graduate Systems Engineer
Often replies in 3 daysTBG Solutions LtdBarlborough S43- Flexitime
- Referral programme
- Annual leave
- Employee discount
- Free parking
- Additional leave
- From understanding customer requirements and developing software through to testing, integration and commissioning, you’ll gain valuable practical experience…
- Xstrahl LtdWalsall WS8 7DG
- The engineer must be able to communicate clearly and confidently, technical aspects of their work to physicists, scientists, and medical specialists.
- Domain: Class III medical device · Validation and quality assurance.
- Involvement in validating medical device systems that support patient safety and clinical…
- Gold GroupFalmouth
- Verification & validation testing of medical devices.
- Experience in electronic design within medical devices or regulated industries.
View similar jobs with this employerSThreeManchester- System Validation Engineer opportunities in medical device development typically sit within quality-focused teams delivering Class III medical devices under ISO…
- Intuitive SurgicalNewcastle upon Tyne
- 5-10 years of experience as a Field Service Engineer, including experience in the medical device industry.
- We have attracted some of the best and brightest on…
- Domain: Class III medical device · validation and compliance.
- Demonstrated experience with ISO 13485 and IEC 62304 in a medical device or comparable regulated…
Job Post Details
Clinical Database Programmer
Job details
Pay information not provided
Annual leave, Work from home, Company events
Full-time
68 Upper Thames Street, London EC4V 3BJ
Full job description
Job Summary :
Purpose-Driven Work
Collaborative Culture
Continuous Growth & Development
Other Employee Benefits
Please note benefits may vary based on country.
What to Expect Next
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 London 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 critical role on our study teams and 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 (EDC) 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.
- 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 is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace? :
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
-
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
-
- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
-
- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
-
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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