Parexel

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...

Lead a clinical operations team in Bengaluru, ensuring high-quality, on-time project delivery. Utilize your substantial clinical research experience to manage, resource, and develop professionals. Drive project success through oversight, consultation, and client liaison in a dynamic CRO environment.

Join Parexel as an EMEA Compliance Officer in Dublin. You will develop and manage the regional compliance program, ensuring adherence to laws and mitigating risks. This role requires strong analytical skills, expertise in EMEA regulations, and excellent stakeholder management. A background in cli...

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...

Join our client's team in Springhouse, PA as a Scientist III in Regulated Immunogenicity & Molecular Bioanalytics. This FSP role requires 3-5 years' experience executing molecular assays like qPCR/dPCR and NGS in a GxP environment. You will generate quality data, ensure compliance, and collaborat...

Seeking an experienced MDM Reltio Engineer in Hyderabad. You will design and implement Reltio solutions, focusing on Trust/Match/Merge rules and data pipelines using Azure Databricks and ADF. The role requires 3+ years of specialized Reltio development expertise and knowledge of key MDM domains. ...