Senior Site Partner 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
Company Description PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time
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
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Job Title : TMF Associate Employment Type :Full time, Permanent Job Reports To : Manager, TMF Operations Department/Unit Name : TMF Operations Job Summary : Responsible for the management of the Trial Master File (TMF) content and associated processes during the
About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research
Who We Are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Worldwide Clinical Trials in Toledo, Spain is seeking an experienced Clinical Operations Site Manager to drive data quality and site performance in multicenter studies. You will ensure timely data submission, manage regulatory documents, support TMF filing, and
Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. For those with medical and/or health/life science interest and background
As a Regulatory Affairs Associate at Parexel Consulting, you will support clinical trial submissions to regulatory authorities, focusing on projects in Brazil. This role offers an opportunity to develop skills in regulatory affairs and clinical research while
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience,
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience,
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience,
The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions comply with
Work Here Matters Everywhere Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Trial Delivery Specialist - Clinical Trial Coordination Our client is a leading global biopharmaceutical company advancing vaccines, general medicines, and specialty medicines to prevent and treat disease. As an