
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
đ„ 20 hours ago
đșđž United States â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Manager
đŠ H1B Visa Sponsor
đ» Ghost score 10%
Where this job comes from
Posted on Parexel's careers page, not through a job board
First seen by Remote Rocketship 20 hours ago
Still open on Parexel's site. Checked 3 minutes ago.

10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Adapt draft site feasibility questionnaires into an electronic survey platform and format them âą Apply branching, conditional logic, and scoring parameters determined by the Feasibility Lead âą Develop survey reporting templates within the survey platform or external systems âą Conduct quality checks on potential investigators before survey outreach âą Cross-check available CDAs before survey launch âą Load identified site lists into the survey management system and ensure planned investigators are included âą Launch surveys and monitor and maintain survey preparation and management âą Reconcile survey status and ensure notes and details are appropriately documented âą Identify, collate, research, and update invalid or missing contact details âą Report and monitor country-level responses to support early risk and mitigation planning âą Execute the agreed site identification strategy, including priority site designation âą Apply the agreed communication strategy and supporting materials âą Facilitate revisions to survey content, scoring parameters, and site and country lists âą Monitor site CDA negotiations and disseminate internal status updates âą Complete survey closure tasks, including site notifications
âą BA or equivalent âą 3-5 years industry related experience
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đ° Series C on 2021-11
â° Full Time
đĄ Mid-level
đ Senior
đ Manager
đŠ H1B Visa Sponsor