An experienced Senior CRA is required for an initial 6 month contract with a global pharma giant. There is potential for this role to be extended beyond the initial 6 months.What you will be doing: Being responsible for the planning and management of all monitoring and site related activities (including all kinds of site visits on-site and remote) to ensure patient safety, trial delivery in time and quality as well as site inspection readiness at any.Developing a Site Engagement Strategy and engaging with clinical investigators/staff to build and maintain strong relationships.Evaluating and screening of high-quality investigational sites to support clinical development programs.Collaborating with internal and CRO study teams as well as third party vendors and supporting Clinical Project Managers in study management tasks.Conducting co-monitoring visits with internal or CRO personnel to ensure quality of trial and initiating preventive/corrective actions where appropriate.Training of CRO and site personnel on trial-specific requirements.What you can bring to the role: Experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role.B.S., M.S. degree in a life science/biological related field preferred.At least 3 years' experience in monitoring of trials in clinical development environment (all trial phases).Strong knowledge of GCP and regulatory requirements.Strong communication skills, excellent command of English, fluency in any additional language would be an asset.Experience in rare disease trials would be beneficial.What you get in return: The opportunity to be part of a hugely successful global pharmaceutical company.Excellent rates of pay.Remote working flexibility.Job Types: Full-time, ContractContract length: 6 monthsExperience: Independent monitoring: 3 years (preferred)Pharmaceutical industry: 5 years (preferred)Language: English (required)#J-18808-Ljbffr