Parexel

Key Requirements: MBBS or MD from a recognized medical school 2+ years of experience in ICSR medical review Good understanding of medical terminology Experience in pharmacovigilance, drug safety, or c

The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and operational data to support the Data Surveillance process and reviewing project-specific Quality Tolerance Limits. They

The Manager is responsible for the oversight of a team or group. This includes ensuring successful performance and delivery of his/her direct report’s project deliverables, on time with high quality.

An initiation Clinical Research Associate (iCRA) specializing in Pre SIV and Activation tasks will be assigned & accountable for managing and driving the strategy for the startup, Pre SIV and Activati

Specialist, Budgeting and Analysis Key Accountabilities: Relationship Management: Work alongside project team to help develop a partnership with all Parexel departments to assist them in their interac

Key Responsibilities: Design and develop systems and data integrations using MuleSoft Anypoint Platform. Design and develop high-quality APIs and Integrations. Develops unit tests and provides code co

Site Start Up EUCTR II Responsible for planning and submitting the complex EUCTR submission i.e. large phase II and III trials with multiple countries and sites. Job Requirements: In addition to the c

Job Purpose: Lead the development and oversight of Medical Services budgets for proposals and contracts, applying advanced expertise and judgment to deliver high-quality, cost-effective solutions. Ana

Contribute to the development of health economic models that evaluate the cost-effectiveness of health technologies for global reimbursement applications. Perform data analysis, assist in model buildi

Job Summary: The Clinical Trial Submission Lead (CTSL) is responsible for end-to-end planning, coordination, and execution of Clinical Trial Applications (CTA) across EU CTR and Rest of the World (ROW