Lead Medical Writer - Latam 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
The Chief Medical Affairs Office’s Evidence Generation (Ev Gen) Platform is responsible for establishing global scientific leadership and stature through the generation of integrated, end-to-end observational real-world evidence serving all therapeutic areas from proof of concept
The position is for a seasoned individual contributor dedicated to supporting the development, digitization and evolution of an Integrated Evidence Plan, evolving that plan & incorporating into relevant governance documents, and other duties. The Head serve
Work Schedule Standard (Mon-Fri) Environmental Conditions Office At Thermo Fisher Scientific Inc., our mission is to make the world healthier, cleaner, and safer. As a Sr CM Analyst I, you will play a pivotal role in
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description : Continually makes efforts to increase knowledge base and professional skills in areas such as programming, technology and techniques, clinical trials, and the pharmaceutical industry by working
Updated : Today Location : Remote, SP, Brazil Job ID : -OTHLOC-7341-2DR - Not ready to apply?- Join our Talent Network Description Principal / Senior Medical Writer - with proven strong clinical document writing experience- Syneos
JOB DESCRIPTION We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and
Xenon7 is seeking a talented and motivated Real-World Evidence (RWE) Data Scientist to join our team. As an RWE Data Scientist, you will play a crucial role in leveraging real-world data to generate insights and evidence
Principal Biostatistician | Clinical Trials | (FSP - Pharma company) Immunology Phase II/III ¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan. Who will you
Principal Biostatistician | Clinical Trials | (FSP - Pharma company) Immunology Phase II/III Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud.
Principal Biostatistician | Clinical Trials | (FSP - Pharma company) Immunology Phase II/III Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud.
Principal Biostatistician | Clinical Trials | (FSP - Pharma company) Immunology Phase II/III Who will you be working with? This global CRO that offers flexible Functional Service Provider (FSP) solutions to a diverse range of clients
Projects Managers are crucial to the success of Clinical Trials managed by Indero. They are the main point of contact internally as well as externally, ensuring all activities and deliverables are completed on time, on budget,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as a Medical Director M-SERM - And lead our efforts in medical safety evaluation and risk management. What You’ll Do: • Maintain understanding of methods for recording
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Description Senior Programmer Analyst Join Us as a Senior Programmer Analyst – Make an Impact at the Forefront of Innovation The Senior Programmer Analyst performs advanced bioinformatics programming activities
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Safety Committee Specialist – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides
Description Principal / Senior Medical Writer - with proven strong clinical document writing experience Principal / Senior Medical Writer - with proven strong clinical document writing experience Syneos Health® is a leading fully-integrated life sciences services