Tele Research Associate (Remote Work)

Primarily a training and development role this position will support and observe clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. This role will have exposure and training in all aspects of the clinical site monitoring services whilst providing monitoring and site management activities for full-service studies assessing for protocol SOP and regulatory compliance. Responsibilities include site management activities to help drive investigative site and patient recruitment compliance and oversight. Conduct remote data review support data query and closure activities support Risk Based Monitoring (RBM) activities assess data collection and (regulatory) document collection perform remote and onsite activities for investigational sites including site contacts qualification initiation monitoring and close out visits under supervision and/or independently and in accordance with corporate sponsor and regulatory (ICH GCP and other) standards and guidelines. Conducts and documents remote site contacts which could include remote site initiation monitoring and close out visits. Conduct remote data review of EDC CTMS RBM and other clinical systems to ensure alignment with SOPs study guidelines and GCP best practices. Remotely monitor resolve and/or facilitate resolution of queries arising out of regular and/or safety reviews adverse events and other data management activities throughout the trial.
Coordinate delivery of clinical sites communications collaborating with project teams to ensure investigational sites are provided accurate ongoing data updates information and feedback on project/regulatory guidelines and objectives throughout the project life cycle.
Site Setup and Startup Support
Identify and recruit site investigators coordinate the movement and delivery of trial materials samples tests and forms including investigational medicinal product protocols SOPs CRFs project documents forms and support tools.
Ensure SOPs in place to optimize patient recruitment providing guidance to site teams of inclusion/exclusion criteria.
Training and Development
Support and observe primary assigned CRAs at both onsite and remote visits.
Support Lead CRAs with remote site management activities.
Participate on all study related activities including but not limited to trainings team meetings and provide any necessary updates to the study team.
For one CRA position supporting Flemish sites in Belgium Dutch language skills are required.
Home-based
We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. If you would like more information about how your data is processed please contact us.