Clinical Programmer

4 weeks ago


United Kingdom Planet Pharma Full time

Title: Lead Clinical Programmer (RAVE)

Company: Biotech

Location: remote based in UK

Employment Type: Permanent


The Lead Clinical Programmer responsible for managing one or more studies. Tasks include designing, developing, and maintaining clinical databases, ensuring compliance with study contracts and SOPs. Key duties involve coding, testing, and documenting databases, integrating external data, and resolving database issues. You’ll collaborate with project teams, manage timelines, support technology upgrades, and maintain core procedures.


Skills and Qualifications:

  • Strong knowledge of ICH GCP and regulatory requirements.
  • Experience with RAVE EDC build.
  • Excellent organizational, communication, and analytical skills.
  • BS in a scientific/health field or equivalent experience.
  • At least one year of study build leadership experience.



  • United Kingdom Worldwide Clinical Trials Full time

    External Description:Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials,...


  • United Kingdom Worldwide Clinical Trials Full time

    External Description: Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical...

  • Statistical Programmer

    2 months ago


    United Kingdom Worldwide Clinical Trials Full time

    External Description:Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials,...


  • United Kingdom Worldwide Clinical Trials Full time

    It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of almost 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. What Global Programming does...

  • Clinical Programmer

    2 weeks ago


    United Kingdom AL Solutions Full time

    About the Role:The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support accurate...

  • Clinical Programmer

    4 days ago


    United Kingdom AL Solutions Full time

    About the Role:The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support accurate...

  • Senior SAS Programmer

    4 weeks ago


    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    1 month ago


    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    1 month ago


    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    1 month ago


    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...

  • Senior SAS Programmer

    1 month ago


    United Kingdom MAC Clinical Research Full time

    We are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...


  • United Kingdom MAC Clinical Research Full time

    supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and...


  • United Kingdom MAC Clinical Research Full time

    supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and...

  • RAVE Programmer

    4 weeks ago


    United Kingdom Planet Pharma Full time

    Planet Pharma is currently recruiting for a Clinical RAVE Programmer to work on a permanent and remote basis in the UK.Main Responsibilities: Acts as the Lead Clinical Programmer Complete Clinical programmer tasks for assigned studies under minimal supervision according to the study contract and applicable SOPs. Design, develop, implement, maintain, and...

  • RAVE Programmer

    2 months ago


    United Kingdom Planet Pharma Full time

    Planet Pharma is currently recruiting for a Clinical RAVE Programmer to work on a permanent and remote basis in the UK.Main Responsibilities: Acts as the Lead Clinical Programmer Complete Clinical programmer tasks for assigned studies under minimal supervision according to the study contract and applicable SOPs. Design, develop, implement, maintain, and...

  • Senior SAS Programmer

    3 weeks ago


    United Kingdom Warman O'Brien Full time

    Senior Statistical Programmer – FSP | Global CRO | Fully Remote | UK | Europe | In this role, you will lead programming activities for complex clinical studies, manage resources, allocate tasks, and track progress to meet project timelines and quality standards. Lead programming for multiple complex studies. 5+ years of experience in statistical...


  • United Kingdom Veramed Full time

    Join Our Team as a Statistical Programming Trainer - R Language! We are excited to invite an experienced Statistical Programming Trainer to develop and implement R language training programs for our permanent SAS programming workforce. This unique role offers the opportunity to make a significant impact within our organization and help shape the future of...


  • united kingdom Clyde Munro Dental Group Full time

    Embark on Your Scottish Dental Adventure: The Overseas Explorer Programme Are you an internationally trained Dentist, ready to explore new horizons and elevate your career? Clyde Munro, Scotland's leading dental group, is excited to launch the Overseas Explorer Programme . This exclusive 1-year support programme is designed to welcome talented...


  • United Kingdom Loveday & Co Full time

    Who We Are Loveday & Co. offers over 100 years of combined experience in elderly care, healthcare and hospitality. Loveday is recognised as the premier provider of luxury care services in London. 37 bed luxury hospitality driven residential nursing care set within a Grade II listed building in 16 acres of landscaped grounds catering to residential nursing...


  • United Kingdom CAPITA HAAS Full time

    Troubles Permanent Disablement Payment Scheme Clinical Assessor RoleWe are seeking a skilled and compassionate Clinical Assessor to join our team at CAPITA HAAS. As a Clinical Assessor, you will play a critical role in evaluating the permanent disablement caused by Troubles-Related Incidents and determining the level of disablement for applicants to the...