Fast Track Your Career, Clinical Trial Manager

Would you like to build your career within one of the 10 top CROs in a world? Our client is looking for Clinical Trial manager to join their teams in Argentina and Brazil, giving you flexibility and an opportunity to progress your career! Sites are in Buenos Aires and Sao Paolo. There is also an option to work fully remote, for those who have 5+ years of...

Due to the constant growth of the company genuine career progression opportunities are offered for the right individual so will be able to gain loads of relevant experience and further your career in no time. You will become part of a global company so will be able to work not only on local but also international studies. Excellent opportunity to take on new...

Our client, a growing and developing global CRO, offering a great opportunity and career progression, is hiring a Clinical Trial Manager.Our client is based around the globe and are in search of someone based in Brazil, with a great list of benefits, which include:- Career progression- Open communication- Work in a top rated CRO- Stable environment- To work...

Clinical Trial ManagerMy Client who is a full-service clinical CRO is currently looking for a Clinical Trial Manager (PM) to join their team in Buenos Aires, Argentina or San Paolo, Brazil. They provide Phase I to IV clinical development services to biotechnology, pharmaceutical and medical devices companies. They offer an industry recognised 2 month...

Clinical Trial Manager My Client who is a full-service clinical CRO is currently looking for a Clinical Trial Manager (PM) to join their team in Buenos Aires, Argentina or San Paolo, Brazil. They provide Phase I to IV clinical development services to biotechnology, pharmaceutical and medical devices companies. They offer an industry recognised 2 month...

Overview We are currently seeking a Senior Manager, Pharmacovigilance to join our diverse and dynamic team. As the Senior Manager in this role at ICON, you will be responsible for overseeing pharmacovigilance activities to ensure the safety and efficacy of our clinical trials. Your leadership will be critical in maintaining compliance with regulatory...

Job Title Key Responsibilities: Act as a primary contact for investigative sites and ensure all documents required are collected in a timely manner. Collect and track all the necessary documents, perform quality reviews, format and compile final documents for effective and compliant site activation and maintenance without supervision. Ensure high-quality...

Strategic Operational LeadThis role plays a key part in the operational strategy and planning process.It involves participation in strategy development conversations, primary and secondary data collection and analysis, and feasibility and site selection strategies development.Key Responsibilities:Supports the analysis, interpretation, and presentation of...

Parexel FSP is hiring multiple Sr CRAs in Brazil The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the...

International Opportunity for Veeva Specialist – Veeva Clinical / Limfinity / JMP Are you a professional ready to take your expertise global?HCLTech is hiring for a high-impact international project in Mexico City, and we're looking for talented individuals with experience in Veeva Clinical, Limfinity LIMS, and JMP.This is your opportunity to work at the...