Parexel - Remote work

Join Parexel as a Senior Clinical Research Associate (CRA) in the United States. You will ensure trial conduct and patient safety, monitoring sites with 60-80% travel. Requires 3+ years monitoring experience, ICH/GCP knowledge, and fluency in English. Work on global projects with career growth in...

Join Parexel's Biostatistics team in Taiwan to support new treatment efficacy and safety. Utilize your statistical expertise in clinical trials, from protocol input to analysis plans. This role offers project leadership, client interaction, and flexible work arrangements. Experience with SAS and ...

Join Parexel as a Senior CRA II in Turkey. Utilize your 5+ years of monitoring experience, ideally in Oncology, to ensure patient safety and GCP compliance. Manage site operations and enjoy a supportive environment with flexible work arrangements. This FSP role offers global project exposure with...

Join Parexel as a Data Surveillance Analyst. Utilize your clinical data experience and SAS/SQL skills to analyze trends and manage risks in a fully flexible, home-based role. You will develop Data Surveillance Plans and present key findings, ensuring study quality and patient welfare. We offer co...

Join Parexel's Patient Safety team in India as a Japanese-speaking Specialist. You will manage adverse event case processing, safety reporting, and ensure compliance with global regulations. This role requires strong drug safety knowledge, analytical skills, and proficiency in database searches. ...

Join Parexel Consulting as a Regulatory Affairs Consultant specializing in Labelling. Utilize your 8+ years of industry experience to develop global regulatory strategies for biopharmaceutical and medical device clients. This remote role in Australia offers diverse client exposure, career growth,...

Lead global clinical trials for Biotech clients at Parexel. This project leadership role requires 2+ years of CRO/Biotech experience managing cross-functional teams, budgets, and timelines. Enjoy a supportive, flexible environment with diverse therapeutic areas and clear career progression in the...

Lead global clinical trials as a Project Leader at Parexel's Biotech Division. This remote US role requires 2+ years of CRO/biotech experience managing cross-functional teams, budgets, and timelines. Enjoy a supportive, empowered environment with flexible work arrangements and diverse therapeutic...

Join Parexel as a Senior Regulatory Associate. Leverage your 5+ years of Regulatory Affairs CMC experience to develop global strategies for biopharma clients. Author key submissions and ensure compliance across multiple regions. Enjoy flexible work, career growth, and a supportive global environm...

Join Parexel as a Senior Statistical Programmer in Poland or Serbia. Utilize your 5+ years of SAS programming and CDISC expertise to analyze clinical trial data. Enjoy a supportive environment with flexible work, career growth, and performance bonuses. Help accelerate new treatments for patients.

Join Parexel as a Clinical Research Associate (CRA) in South Korea. You will monitor clinical trial sites, ensuring patient safety and protocol integrity. We require fluency in Japanese and Korean (or Taiwanese Mandarin), a life sciences degree, and site management experience. Enjoy a patient-foc...

Join Parexel as a Senior Statistical Programmer, fully home-based in Serbia. Utilize your 5+ years of SAS programming and CDISC expertise to analyze clinical trial data and support submissions. Enjoy a flexible role with extensive training, a supportive environment, and long-term career growth in...