Job Overview: Our FSO team is seeking an Ophthalmology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory experience in
Job Overview: Our FSO team is seeking an Oncology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory experience in
Job Overview: Our FSO team is seeking a General Medicine Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory experience
Under moderate supervision, the Regulatory and Start Up Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages
Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. The Contract Specialist
Principal Medical Writer 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
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
Are you a Clinical Research Manager with hands-on ophthalmology trial experience looking to lead at country and site level on cutting-edge retina studies? This role is for someone who already owns CRM delivery end-to-end and wants
The Clinical Study Administrator (CSA) plays a crucial role in coordinating study activities from start-up to execution and close-out within Country Operations Management (COM). This ensures the quality and consistency of trial deliverables, meeting time, cost,
Our Senior Associate I (Regulatory Affairs Senior Analyst) is actively accountable in daily activities to ensure on time business support such as (but not limited to): - Elaboration of New Synthetic and New Biological medicines dossiers
CEVA Logistics provides global supply chain solutions to connect people, products, and providers all around the world. Present in 170+ countries and with more than 110,000 employees spread over 1,500 sites, we are proud to be
JOB DESCRIPTION Buscamos talentos que possam transformar possibilidades em realidade, que contribuam para nos manter como a melhor e mais completa empresa farmacêutica brasileira, participando da vida das pessoas para que elas vivam mais e melhor.
Buscamos talentos que possam transformar possibilidades em realidade, que contribuam para nos manter como a melhor e mais completa empresa farmacêutica brasileira, participando da vida das pessoas para que elas vivam mais e melhor. Todas as