Parexel

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. ...

Join our finance team in Hyderabad as a Cash Management Specialist. You will manage Oracle cash modules, perform critical bank reconciliations, and ensure timely monthly closes. The role requires 1-3 years' experience, strong accounting knowledge, and reconciliation skills. Ideal candidates are a...

Join Parexel's Statistical Programming team in Hyderabad as a Statistical Programmer II. You will analyze clinical trial data using SAS to assess safety and efficacy across diverse therapeutic areas. This role requires strong analytical skills, proficiency in SAS, and knowledge of ICH-GCP. We off...

Join Parexel in Hyderabad as a Senior Statistical Programmer. Lead projects, analyze clinical trial data, and ensure safety/efficacy assessments. Enjoy extensive training, a supportive environment, and diverse therapeutic exposure. Leverage your SAS skills to help bring new treatments to patients...

Lead cross-functional teams to deliver patient-focused clinical trials in Rixensart. This senior project specialist role requires a science degree and strong project management skills. You will ensure quality, manage timelines, and drive life-changing treatments to market. Enjoy a supportive envi...

Seeking a Site Contract Associate II in Bengaluru to manage clinical trial site agreements. You will draft, negotiate, and finalize contracts, ensuring compliance and protecting client interests. The role requires 2-5 years of CRO experience, strong legal/analytical skills, and fluency in English.