Acts as the primary point of contact for trial-specific medical and safety-related questions.
Monitors trial participant safety and provides medical expertise to global clinical studies.
Reviews protocols, safety reports, and clinical study documents while supporting audits and investigator meetings.
PSI is a leading Contract Research Organization with more than 30 years of industry experience, offering a balance between stability and innovation. The company focuses on delivering quality and on-time services across therapeutic indications and is part of an international group of medical professionals.
Serve as the senior EMEA medical expert for CRRT, extracorporeal blood purification, CO2 removal, and anticoagulation.
Lead evidence-generation planning, real-world evidence activities, and scientific communication to shape acute therapy strategy.
Build influential partnerships with key opinion leaders, professional societies, and clinical networks across EMEA.
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. With a nearly 70-year legacy in kidney care, Vantive is building a purpose-driven culture focused on meaningful innovation and improving patients' lives worldwide.
Provide as-needed hematology consultations for clinical trial participants with neutropenia events.
Review blood test results including ANC and recommend appropriate medical follow-up.
Document assessments accurately per study protocols, GCP, and FDA regulations.
Adams Clinical is a clinical trial site network focused on advancing healthcare through high-quality clinical research and diverse patient enrollment. The company emphasizes a culture of respect, transparency, and continuous improvement, with a team dedicated to improving lives through innovation and integrity.
Serve as primary medical and scientific expert for clinical trial protocols and Expanded Access Programs.
Monitor trials to ensure participant safety, data accuracy, and protocol compliance.
Lead protocol development, investigator training, and cross-functional collaboration.
WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trials, expanded access programs, and market access solutions. With 15+ years of experience across 150+ countries, they offer operational scale and a personalised culture.
Provide medical oversight for clinical trials, safeguarding participant safety and ensuring protocol compliance.
Review adverse events and safety data, contributing to regulatory reporting and clinical documentation.
Collaborate with investigators and clinical teams to support study design, execution, and risk management.
This position is listed on behalf of a partner company that manages all applications and next steps. The role supports global clinical research in a remote working environment with cross-functional collaboration.
Provide medical direction and oversight for clinical trials, including safety monitoring and medical data review.
Partner with GCO to build client relationships and support proposals, feasibility, and business development.
Serve as drug development SME, contributing to protocols, training, and medical strategy across studies.
Fortrea is a global contract research organization providing clinical development and trial management services to pharma/biotech. It fosters a collaborative, family-like culture focused on advancing life-saving therapies.