iconplc - IT - Software Development, Hybrid work

Join ICON plc in Shanghai as a Clinical Research Associate II. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and drive clinical innovation. Enjoy benefits like health insurance, retirement planning, and global employee support. Advanc...

Senior Clinical Python Programmer sought by ICON plc in Bangalore, India. Leverage 4+ years of experience in clinical data, Python, and SDTM to lead data science solutions for clinical trials. Drive innovation with PySpark, Spotfire, or Power BI in a dynamic, inclusive environment. Enjoy competit...

Seeking a skilled Biopharm Clinical Research Associate in Taipei, Taiwan. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring ICH-GCP compliance and patient safety. Requires a Bachelor's in science/healthcare and 2+ years of CRA experience with strong organ...

Senior Project Manager (Laboratory) sought by ICON in Blue Bell, PA. Lead clinical trial design, analyze complex medical data, and oversee lab operations to ensure quality and timeline adherence. Requires 5+ years in clinical labs/trials, 3+ years PM experience, and a life sciences degree. Enjoy ...

Regulatory Affairs Specialist needed in Bogota, Colombia. Join ICON, a world-leading clinical research organization. You will manage regulatory submissions, amendments, and health record maintenance for Colombian authorities. Requires a Pharmaceutical Chemist degree, 1+ year of regulatory experie...

ICON seeks a Clinical Research Associate II in Hangzhou, China, to design and analyze clinical trials. You will ensure protocol compliance, data integrity, and patient safety while conducting site visits. Requires a Bachelor’s degree, 2+ years of CRA experience, and ICH-GCP knowledge. Benefits in...

Join ICON plc as a Clinical Data Coordinator I in Warsaw, Poland. You will design and analyze clinical trials, interpret medical data, and support innovative treatments. Requires a Master’s in Life Sciences or Healthcare, basic clinical data management knowledge, and familiarity with Medidata or ...

Join our team as a Senior Clinical Validation Analyst in Bangalore. Utilize your 5+ years of EDC expertise, primarily in Medidata Rave, to validate and test clinical trial systems. You will lead UAT coordination, ensure compliance, and support study builds. We offer competitive health insurance, ...

Seeking a Senior Data Scientist specializing in Data Management for an office-based role in Blue Bell, PA or Raleigh, NC. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient linkage methodologies. This role offers competitive benefits and the chance t...