Parexel - Remote work

Lead our clinical data management for late-phase oncology trials. This role requires 7+ years of pharmaceutical/biotech data management experience, strong project oversight, and CDISC/ICH-GCP proficiency. You will develop risk strategies, ensure data quality, and collaborate with stakeholders. Id...

Join our global team as a Study Physician in Oncology. This critical role provides medical oversight for clinical trials from design to reporting. We seek a qualified physician with pharma/CRO experience and strong analytical skills. This is a US-based position within a collaborative, internation...

Join Parexel's global oncology team as a Medical Director. Utilize your US/Canada board certification to provide expert medical monitoring and safety oversight for cutting-edge cancer trials. This role offers the chance to impact novel therapies, including immuno-oncology, with some travel requir...

Seeking a remote Clinical Study Physician specializing in Oncology. This global role requires an MD with 4+ years of clinical experience and industry/CRO background. You will provide critical medical oversight from trial design to reporting. Enjoy flexible work arrangements and a focus on profess...

Parexel seeks a US/Canadian Board-certified Ophthalmologist to join as a Medical Director. Provide expert medical monitoring, client consultation, and leadership in global ophthalmic drug development. Enjoy a flexible, remote role with a focus on professional growth and a client-focused approach.

Join Parexel in Germany as a Study Physician for key Oncology trials. Provide medical oversight from protocol design to final report, ensuring high-quality data. Requires an MD with 4+ years of clinical practice and ideally industry/CRO experience. This core role offers a chance to shape clinical...

Join Parexel as a Statistical Programmer II, leveraging your SAS expertise (Base, Macro, Graph) and CDISC knowledge (ADaM, SDTM) in clinical trials. This fully remote role in South Africa offers growth through mentorship in a diverse, innovative culture. Contribute to life-changing research, ensu...

Join Parexel as a Senior Medical Writer in the US. Utilize your scientific expertise to author key clinical documents like protocols, study reports, and CTD summaries. This role requires strong writing skills, ICH-GCP knowledge, and collaboration within cross-functional teams. Benefit from a supp...

Lead statistical strategy for global clinical trials as a Senior Manager at Parexel. Utilize your PhD/MS in Statistics and SAS expertise to design studies and ensure regulatory compliance. Enjoy a flexible, supportive environment in Argentina with diverse project exposure and career growth opport...

Join our team in Brazil as a Site Contract Associate. You will draft, negotiate, and finalize clinical trial site agreements, ensuring compliance and protecting client interests. The role requires 2-5 years of CRO experience, a relevant degree, and fluency in English. Utilize your legal and negot...

Join Parexel as a Document Specialist, supporting critical clinical research from a remote Canada position. Utilize your expertise in clinical document formatting and publishing software to ensure submission-ready deliverables. This role offers continuous learning, career growth, and a patient-fo...

Lead centralized monitoring for global clinical trials as a Manager, Data Analysis. Configure and maintain RBQM systems, utilizing programming expertise in R, SQL, or SAS for advanced data analysis and KRI/KPI reporting. This US-based role requires 4+ years of pharma experience and direct RBQM sy...