Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
Human Resources Associate Department: Human Resources Employment Type: Full Time Location: Milan, IL (4905) Reporting To: Amanda Laffoon Compensation: $21.00 - $24.00 / hour Description Are you passionate about helping people and creating exceptional employee experiences? Do
Line of ServiceAdvisory Industry/SectorFS X-Sector SpecialismRisk Management LevelSenior Associate Job Description & Summary Focused on relationships, you are building meaningful client connections, and learning how to manage and inspire others. Navigating increasingly complex situations, you are growing
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Sr. Site Contracts Associate IQVIA Biotech Italy - Homebased IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise
Line of ServiceAdvisory Industry/SectorNot Applicable SpecialismDeals Management LevelAssociate Job Description & SummaryPwC Advisory Corporate Finance supporta clienti industriali e finanziari nelle operazioni di finanza straordinaria, tra cui acquisizioni, dismissioni, ristrutturazioni e operazioni strategiche complesse. All’interno di
About the role: Gartner’s Consulting business is an extension of Gartner’s industry-leading IT Research. From CIOs, to leaders in business and government, we help Gartner clients across enterprises translate insights into transformational actions and achieve their mission-critical
About the role: Gartner’s Consulting business is an extension of Gartner’s industry-leading IT Research. From CIOs, to leaders in business and government, we help Gartner clients across enterprises translate insights into transformational actions and achieve their mission-critical
Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary Of Responsibilities Responsible for all
Fortrea is seeking a Senior Clinical Research Associate to lead site monitoring and site management for multicenter clinical studies in Italy. You will ensure adherence to company and sponsor SOPs, regulatory guidelines, and study plans, while coordinating with
Clinical Research Associate, Sponsor Dedicated – Italy Join to apply for the Clinical Research Associate, Sponsor Dedicated – Italy role at IQVIA Responsibilities Performing site selection, initiation, monitoring and close‑out visits Supporting the development of a subject recruitment plan Evaluating
IQVIA seeks an Experienced Clinical Research Associate to work from home in Italy. You will perform site monitoring and site management to ensure studies are conducted per protocol, GCP, and ICH guidelines. You will coordinate monitoring visits and
Senior Clinical Research Associate 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 at the
BeOne Medicine is seeking an experienced Clinical Research Associate to monitor oncology/hematology trials across sites. You will perform feasibility, site selection, and monitoring visits in line with ICH-GCP and internal SOPs, ensuring data quality and safety. Collaboration with
Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
We are looking for a motivated Clinical Research professional to join our Clinical Operations team. This role is designed for someone with a scientific/life sciences degree and initial experience in clinical research, such as a Clinical Trial Assistant