Senior Clinical Programmer

TN United Kingdom; United Kingdom; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player seeks two Senior Clinical Programmers to enhance their Global Data Management team in the UK. This exciting role involves leading clinical programming tasks, developing and maintaining clinical database systems, and providing technical expertise to clients. The ideal candidate will possess a strong understanding of regulatory requirements and excellent organizational skills. Join a diverse and inclusive workplace that values innovation and collaboration, offering a unique opportunity to contribute to significant advancements in healthcare.

Qualifications

• Minimum BS in a scientific or health related field or equivalent experience.
• Previous experience as a clinical database developer with leadership experience.

Responsibilities

• Lead Clinical Programmer for multiple studies, ensuring compliance with SOPs.
• Design, develop, and maintain clinical database systems.
• Interface with project teams and external vendors to negotiate timelines.

Skills

Clinical Database Development

Regulatory Compliance

Data Analysis

Communication Skills

Education

Bachelor's Degree in Scientific or Health Related Field

Job description

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Senior Clinical Programmer, united kingdom

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Client:

ProPharma Group

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

baae10def8e9

Job Views:

9

Posted:

26.04.2025

Expiry Date:

10.06.2025

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Job Description:

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Due to growth, we have an immediate need for 2 Senior Clinical Programmers to join our Global Data Management team in the UK.

The Senior Clinical Programmer position is responsible for providing database development services to ProPharma clients.

Main Responsibilities:

• Acts as the Lead Clinical Programmer for one or multiple studies.
• Complete Clinical programmer tasks for assigned studies under minimal supervision according to the study contract and applicable SOPs.
• Design, develop, implement, maintain, and support clinical database systems.
• Offer technical expertise for internal and external clients.
• Code, test, and document databases as per programming standards and clinical validation policies.
• Program database manipulation and conduct data transfers for clients.
• Review Data Validation Plans and Case Report Forms as per area of expertise.
• Add all external data sources such as PK and central lab within the clinical database if integration is requested or required.
• Serve as programming contact to handle database issues within area of expertise.
• Support development and implementation of new technologies.
• Support Information Technology to evaluate new technology upgrades by participating in software change controls.
• Support development, revision and maintenance of core operating procedures and working instructions pertaining to database. development, user acceptance testing and change controls.
• Interface with project team to organize responsibilities and deliverables.
• Establish effective communication and professional relationships with teams and external vendors.
• Interface with Clinical Data Management and corporate team to negotiate timelines.
• Perform administrative tasks within the EDC system, such as site and user management, URL level reviews and/or approvals, and dictionary updates.
• Follow and influence the development of data standards and strategies pertaining to the standards library.

Necessary Skills and Abilities:

• Understanding of the principles of ICH GCP and regulatory requirements is essential.
• Excellent organizational and analytical skills, strong oral and written communication skills, and able to work in a high paced, timeline driven setting.

Educational Requirements:

• Minimum BS in a scientific or health related field or equivalent in years of experience.

Experience Requirements :

• Previous experience as a clinical database developer with at least one year of experience leading a study build.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***