Parexel - Remote work

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...

Lead cross-functional clinical trial teams as a Project Specialist at Parexel in Colombia. Utilize your strong project management, Excel, and English skills to drive study delivery and financial metrics. Enjoy a flexible, supportive environment with professional growth opportunities while helping...

Join Parexel as an Investigator Financial Analyst II in the United States. You will steer investigator budget management for crucial clinical projects, translating clinical conduct into financial impact. This role offers a collaborative environment, comprehensive benefits, and flexible working ho...

Lead global clinical trial site activation for a pharmaceutical sponsor. Utilize your 4-6 years of regulatory submission and project management experience in Pharma/CRO. Based in Serbia, you will develop strategies, oversee CRO performance, and ensure efficient, compliant study start-up.