Responsibilities Ensure the clinical consistency of data used for statistical analyses and clinical study reports Clinical data to be check includes (but not limited to): laboratory results, adverse events, medical...

Ensure the clinical consistency of data used for statistical analyses and clinical study reports Clinical data to be check includes (but not limited to): laboratory results, adverse events, medical history, vital...

Veeva’s Consultant Development Program (CDP) is an accelerated pathway that transforms early-career professionals into high-impact consultants who deliver cloud and AI solutions, helping global Life Sciences companies...

Job Description: About the role: At Takeda, we are a forward‑looking, world‑class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic...

Reporting to the Head of Quality & Regulatory Affairs France / BeNeLux – Pharmacien Responsable, the Regulatory Affairs & Quality Assurance - PRI support the Exploitant for : Taking part into the implementation,...

Pierre Fabre Laboratories, a global leader in dermo-pharmacology, seeks a Clinical Scientist- R&D Pharma to support Clinical Medical Monitoring in oncology trials. Based in Toulouse (Langlade), you will contribute to...

Flexible working This Job is based in Australia Employment Type Full Time, 35 hours per week Duration 3 Years Fixed Term Remuneration Research Level C or D ($155K- $185K) based on experience + 17% Super + Annual leave...