Meet today's talent at ARC

After graduating from Queens with a Degree in Medicine James Lappin worked as a Doctor in the NHS for 5 years working across a variety of specialties across Northern Ireland. After this James moved to an advisory role at a private health clinic where he fulfilled various functions within the role including quality management, leadership team, client safety, results reporting and training. As the Associate Director Global Regulatory Compliance - Translational Biomarkers, I am responsible for supporting ARC’s clinical consulting service provision, ensuring that client's medical device research is conducted and reported in compliance with global GCP standards, and assisted in the development of medical device technical documentation.

Since early on in life David has always wanted to help people; he thought he could achieve this best through charity and working in Life Sciences. After graduating from University of Bradford with a BSc in Biomedical Science, David started his career as an Animal Technician helping develop and produce vaccines, QC and efficiency tests for animals before moving on to human health. David went on to work for Merck and Veeda Laboratories before he joined ICON development Solutions as a Project Lead for biomarker assays for drug development Phase I-IV clinical trials. David then progressed onto a Senior Project Manager position in QIAGEN introducing CDx products to market such as EGFR, EGFR rare mutations and PIK3CA. Prior to joining the ARC team David also spent a year at Diaceutics and NAMSA bringing several products to market.

After graduating from Queens with a Degree in Medicine James Lappin worked as a Doctor in the NHS for 5 years working across a variety of specialties across Northern Ireland. After this James moved to an advisory role at a private health clinic where he fulfilled various functions within the role including quality management, leadership team, client safety, results reporting and training. As the Associate Director Global Regulatory Compliance - Translational Biomarkers, I am responsible for supporting ARC’s clinical consulting service provision, ensuring that client's medical device research is conducted and reported in compliance with global GCP standards, and assisted in the development of medical device technical documentation.

Since early on in life David has always wanted to help people; he thought he could achieve this best through charity and working in Life Sciences. After graduating from University of Bradford with a BSc in Biomedical Science, David started his career as an Animal Technician helping develop and produce vaccines, QC and efficiency tests for animals before moving on to human health. David went on to work for Merck and Veeda Laboratories before he joined ICON development Solutions as a Project Lead for biomarker assays for drug development Phase I-IV clinical trials. David then progressed onto a Senior Project Manager position in QIAGEN introducing CDx products to market such as EGFR, EGFR rare mutations and PIK3CA. Prior to joining the ARC team David also spent a year at Diaceutics and NAMSA bringing several products to market.