Parexel

Parexel seeks a Site Contract Associate II to join its Site Contracts team, supporting the DACH region remotely from Serbia or Romania. This role requires fluent German and English, focusing on negotiating, finalizing, and executing clinical study agreements and amendments. Ideal candidates posse...

Senior Manager, Third Party Quality Lead (FSP) sought in Brazil. Leverage 7+ years of pharma experience to oversee GCP quality risk management for clinical trial vendors. Drive compliance, audits, and CAPA processes while fostering a culture of quality. Lead global quality discussions and ensure ...

Senior Clinical Research Associate sought in Israel for a dedicated client role. Leverage 5+ years of oncology and site management expertise to oversee all monitoring visits. Join Parexel to mentor junior CRAs, work with world-class technology, and drive global drug development. Enjoy a premium s...

Join Parexel as a Regulatory Affairs Consultant (Labelling) for a remote role in Switzerland. Leverage your German fluency and CCDS expertise to manage global labelling lifecycles for biopharma clients. Drive regulatory strategies, ensure Swissmedic compliance, and support harmonization in a coll...

Parexel seeks a Workday Change Management Specialist to drive global HCM adoption. You will develop communications and training materials for diverse audiences, leveraging AI tools and SharePoint. Ideal candidates have 2-3 years of change management experience and Workday HCM knowledge. This UK-b...

Join a leading Early Phase Clinical Unit in Berlin as an Associate Clinical Research Physician. You will act as co-investigator on Phase I/II trials, ensuring participant safety and regulatory compliance (ICH-GCP, German Drug Law). We require a medical degree (Approbation), fluency in English and...

Fixed Assets Specialist needed in Hyderabad to manage asset registers, depreciation, and reconciliations. Requires 1-3 years of accounting experience, Excel proficiency, and strong communication skills. Oracle, GL, or R2R experience is a plus. Join a collaborative team ensuring SOX compliance and...

We are seeking a detail-oriented Depot Technician in Schönefeld, Germany, to manage clinical trial materials. You will handle receiving, stocking, picking, packing, and dispatching, while ensuring strict GxP and SOP compliance. Ideal candidates possess warehouse/logistics experience, strong organ...

Join Parexel as an Initiation Clinical Research Associate in Brazil. We seek a detail-oriented, self-starter with strong problem-solving skills to manage site start-up activities, including CDA negotiation and TMF management. This role offers flexible work arrangements and requires excellent comm...

Join Parexel as a Site Care Partner (CRA) in the United States and accelerate patient access to life-changing treatments. Leverage your GCP/ICH expertise to manage investigator sites, drive start-up activities, and build strong cross-functional relationships. We seek a detail-oriented, self-start...

Join Parexel in Buenos Aires as a Desktop Support Technician. Provide first-level IT support, configure laptops, and deploy workstations in a clinical research environment. Requires 1-2 years of experience, Windows/macOS proficiency, and advanced English. Grow your career with a global leader adv...

Join Parexel as a Clinical Research Associate (CRA) in Early Development Oncology, covering the Northeast US. Leverage your 3+ years of site monitoring experience and GCP/FDA expertise to oversee clinical trials from activation to database lock. Enjoy 60-80% travel, flexible work arrangements, an...