Clinical Trial Coordinator

OverviewWe are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc.In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines.As a leader in our research department, you will...

THIS IS A ROLE FOR SOMEONE OPEN TO WORK AS A CONSULTANT FREELANCER LONG TERM FOR TOP PLAYER IN MEDICAL DEVICES. Do you have a first experience in contracting activities for clinical trials ? Are you enthusiastic about clinical trial contracts, budgeting and site negotiation ? You like working in a dynamic, international environment where your strong...

Seeking a skilled contract professional for long-term freelance work with a leading medical device company.Key Responsibilities:Draft and review clinical trial agreements, negotiate terms, and finalize contractsEnsure compliance throughout the contract management processCoordinate with site staff, study teams, legal departments, and finance teamsMaintain...

Job Title: Senior Executive / Specialist - Case Processing Employment Type: Contract About ClinChoice ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and...

OverviewSr CRA II - Sponsor dedicated - Brazil Home BasedJoin to apply for the Sr CRA II - Sponsor dedicated - Brazil Home Based role at Syneos HealthSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.We translate unique clinical, medical affairs and commercial insights into outcomes to...

Job Overview The Senior Regulatory Specialist will be the primary contact with investigative sites during site start-up activities and maintenance. This role is responsible for collecting required documents, ensuring EC/IRB/Third body/Regulatory Authority applications are made within agreed timelines, and that documentation meets applicable regulations and...

OBJETIVO DA POSIÇÃO: Garantir continuidade dos processos junto aos Centros LATAM , através do acompanhamento e da supervisão dos estudos clínicos Assegurar que as práticas e os procedimentos operacionais sejam seguidos corretamente, tanto de forma presencial quanto remota, contribuindo para a melhoria da performance e qualidade das operações dos...

Job OverviewThe Global Feasibility Lead II will play an integral role in operational strategy and planning in the preaward space through participation in strategy development conversations, robust primary and secondary data collection and analysis, and development of feasibility and site selection strategies.In addition, the Global Feasibility Lead II will...

Global Feasibility Lead Ii - Detalhes da Vaga. ? In addition, the Global Feasibility Lead II will be responsible for managing global feasibility projects, working closely with representatives within the company to deliver robust feasibility reports to our customers. ? The Global Feasibility Lead II will transition the site selection strategy to operations in...

Bring more to life.Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.You'll thrive in a culture of belonging where...