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,...

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.

Seeking a Senior Power Apps Developer with 6+ years in the Clinical domain. You will design and develop complex solutions using Microsoft Power Platform (Power Apps, Automate, BI) and SharePoint. This India-based role requires strong technical skills and offers the chance to support key business ...

Seeking a skilled Program Coordinator to provide expert project support for an Account Team. This remote role in India requires advanced MS Office skills and strong organizational abilities to manage multiple projects within deadlines. Experience in medical communications is a plus. Join a compan...

Seeking a Scientific Specialist with 5-8 years of medical communications experience. This remote role in India involves developing high-quality scientific content and managing projects for key clients. Ideal candidates possess a Life Sciences degree, strong writing skills, and expertise in data i...

Seeking a Senior Physician in Patient Safety to provide expert pharmacovigilance and medical review for clinical trials and post-marketing products. This remote role in Canada/US requires an MD with 3-5 years of drug safety experience and board certification. You will ensure regulatory compliance...