Parexel - Remote work

Seeking a Senior Data Engineer in India to design and implement robust data solutions on Microsoft Azure. You will leverage expertise in Azure SQL, Synapse, and ETL tools like Qlik and Informatica to ensure data quality and performance. This role involves complex database development, systems int...

Lead GCP quality oversight for clinical trial programs as an Asset Quality Director. Utilize your 10+ years of experience in ICH GCP and risk management to ensure compliance and inspection readiness. This remote role in Argentina requires strategic use of quality data to guide cross-functional st...

Join Parexel Consulting as a Regulatory Affairs Consultant. Leverage your 4-6+ years of CMC regulatory experience to develop strategies for FDA/EMA submissions. Enjoy a fully remote role in the US with flexible work arrangements and global client exposure. Drive product approvals in a supportive,...

Join Parexel as a Clinical Research Associate (CRA) in South Korea. You will ensure patient safety and protocol adherence while managing investigator sites on global projects. We seek degree-qualified candidates with site management experience and strong problem-solving skills. Enjoy flexible wor...

Lead global clinical trials in Oncology or Immunology at Parexel Germany. Utilize your 6+ years of trial management expertise to drive study delivery from planning through execution. Enjoy a supportive, flexible environment with diverse projects and clear career progression. Empower patients by b...

Join Parexel as a Senior/Principal Medical Writer in this FSP role. Author key clinical documents like study reports for regulatory submissions. Enjoy a supportive culture, career development, and competitive benefits including private healthcare. Ideal for a life sciences graduate with excellent...

Lead Site Monitoring and Clinical Operations for global trials in Germany. Utilize your life sciences degree and extensive monitoring expertise to ensure patient safety, protocol compliance, and inspection readiness. Drive risk-based strategies within a supportive, patient-focused environment off...

Join Parexel as a Clinical Study Team Assistant. You will manage the Trial Master File (TMF), ensuring compliance with ICH-GCP and SOPs. This remote/hybrid role requires 2-3 years of clinical administration experience and strong organizational skills. Enjoy a supportive, flexible environment with...

Lead RWD strategy for clinical research across EMEA. This hands-on expert role requires 5+ years in pharma/CRO and strong data analytics. You will develop fit-for-purpose real-world data solutions and manage client and data provider relationships. An advanced degree in life sciences or data scien...