Parexel

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...

Join our team as a Data Surveillance Analyst in South Africa. Utilize your SAS/SQL skills and CluePoints experience to analyze clinical data, identify risks, and support monitoring plans. Enjoy a fully flexible, remote role with competitive benefits and a focus on work-life balance.

Join our Baltimore Early Phase Clinical Unit as a Clinical Research Nurse. Administer novel compounds and monitor participant safety in first-in-human trials. Requires an active Maryland RN license, 2+ years clinical experience, and BLS/ACLS certification. We offer competitive benefits, a bonus p...

Seeking a Microbiologist with an Environmental Monitoring focus for a long-term FSP role in Rahway, NJ. This onsite position requires a Bachelor's degree and 2+ years of GMP pharmaceutical microbiology experience, including EM sampling and technical writing. The role offers full benefits, PTO, an...

Join our team in Australia as a Feasibility Specialist for clinical trials. You will conduct research and data analysis to identify optimal trial sites and investigators. This role requires business proficiency in Korean and English, along with expertise in clinical systems (CTMS) and stakeholder...