Clinical Research Jobs in International

Job descriptionWoodston Personnel are seeking an experienced and dedicated Consultant Paediatric Radiologist to join a leading healthcare institution in Saudi Arabia. This Physician will be responsible for performing procedural and consultative duties assigned by the Department Chairman and Section...

Job descriptionWoodston Personnel are seeking an experienced and accomplished Consultant in Womens Imaging to join a prestigious hospital in Saudi Arabia. This physician is responsible for performing procedural and consultative duties assigned by the Department Chairman and Section Head. Main Duties...

Job descriptionWoodston Personnel are seeking a highly qualified and experienced Consultant in Nuclear Medicine to join a prestigious hospital in Saudi Arabia. This is an exceptional opportunity for an accomplished Nuclear Medicine physician to contribute to the delivery of advanced diagnostic and t...

Job descriptionWoodston Personnel are seeking an experienced and accomplished Consultant Interventional Neuroradiologist to join a prestigious hospital in Saudi Arabia. This is an outstanding opportunity to contribute to an advanced neurosciences programme within a world-class clinical environment e...

Leads and manages all facets of customer relationships and account strategy across a portfolio of commercial and security hardware accounts. Drives the execution of integrated programs that align field marketing initiatives with sales objectives to maximize the impact of company products within comm...

PRIMARY FUNCTIONThe Sr. MSL serves to advance science and standards of care for patients healthcare providers and payers and ensure they can access all the practical and clinically relevant information and solutions they need to use  AbbVies products efficiently and safely. Collectively as members o...

The Senior Medical Director will lead late-stage clinical development programs in Oncology including pivotal Phase III trials and registration studies. Responsibilities include independently contributing to and executing on the clinical strategy serving as Medical Monitor supporting regulatory submi...

Start your career in clinical research streamlining communication maintaining systems and managing documents & information.Office-based - ZagrebThe scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling procur...

The Research Compliance Coordinator reflects the mission vision and values of Northwestern Medicine adheres to the organizations Code of Ethics and Corporate Compliance Program and complies with all relevant policies procedures guidelines and all other regulatory and accreditation standards.The Rese...

Union: Non-UnionNew or Replacement: NewNumber of Vacancies: 1Site: Toronto General Hospital Department: DMOHReports to: Senior Research Program Manager Hours: 37.5 hours per weekSalary: $27.56 to $41.34 per hourShifts: DayStatus: Permanent Full-time Closing Date: February 20 2026Position SummaryThis...

The HTA Writer is responsible for providing clinical EUHTA document support to the JCA core team ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process.Provides HTA writing expertise for multiple compounds and/or projec...

Hybrid role in Mississauga ON CanadaSite ManagementEnsures exchange of information and documentation with sites and vendorsEnsures order receipt inventory storage distribution return/recall and reconciliation of clinical suppliesEnsures regulatory and ethics committee submissions and notificationsEn...

Te Whiwhinga mahi The opportunityWe are seeking a Research Assistant Neurogenetics to support research activities within the School of Medicine in the Faculty of Medical and Health this role you will contribute to neurogenetics research by assisting with data collection data entry participant coo...

The Clinical Systems Manager will provide leadership change management and expert level support and maintenance in the administration and optimisation of clinical trial systems and digital platforms to prioritise and ensure the efficient use of operational and business resources and services.The Cli...

Union: Non-UnionNew or Replacement Role: ReplacementNumber of vacancies: 1Site: Toronto Rehab - University CentreDepartment: Fellowship & Education Special ProjectSalary:   $28.42 to $35.52 per hourReports to: Program Medical DirectorHours: 37.5 hr/weekShifts: Monday to Friday 8:30am to 4:30pmStatus...

Job SummaryWestern Digital is seeking a seasoned Government Affairs & Policy Manager to lead its public policy engagement and regulatory strategy in Malaysia. This role will be instrumental in shaping the companys relationship with government stakeholders regulatory bodies and industry associations...

The Regulatory Manager France is responsible for ensuring full compliance with national regulatory requirements and supporting the organizations commercial and operational activities across the French market. This role oversees mandatory declarations labeling and artwork compliance and regulatory c...

Job DescriptionThis role combines the accountability of a clinical research manager and certain elements of a GCTO country lead role. Holders of this position are accountable for:The performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations Our...

Job OverviewDirect a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. Work with senior leadership in formulating effective strategic goals and objectives for designated organization...

Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet c...