Position:Material Planning and Pricing Associate Job Description: Arrow Electronics is a global provider of products, services, and solutions to industrial and commercial users of electronic components and enterprise computing solutions. Arrow Electronics guides innovation forward for over
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Medical Affairs Specialist ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Summary of Responsibilities: To respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Receive information, record, and report Adverse Drug Reaction in timelines (according to the
Job Overview: Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by Fortrea clients to US, EU, Japan, and ROW health authorities and oversight of the same, as applicable. Summary of Responsibilities: These statements are intended to describe
Interested in a career that matters? The Role & Your Impact: Operating in a collaborative and research-focused environment, the role supports scientists and research associates in delivering relevant Household Care application activities. The position combines laboratory studies,
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the
The Senior Pharmacovigilance Analyst will lead the preparation, review, and submission of RPBR/PBRER and PGR/RMP reports, ensuring compliance with global regulations and mentoring junior staff. Key Responsibilities Lead the preparation and submission of RPBR/PBRER and PGR/RMP
The Mid-Level Pharmacovigilance Analyst will manage the preparation and submission of RPBR/PBRER and PGR/RMP reports, ensuring compliance with regulatory requirements and supporting process improvements. Key Responsibilities Prepare and review RPBR/PBRER and PGR/RMP reports independently. Coordinate with
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice