CRA II in Oncology

Syneos Health is seeking a CRA II in Oncology to work in a home-based setting in the Paris area. The successful candidate will be responsible for performing site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance. Key responsibilities include: Evaluating the overall performance of site and site staff, providing recommendations, and escalating serious issues to the project team Verifying the process of obtaining informed consent and protecting subject/patient confidentiality Assessing site processes, conducting source document reviews, and verifying clinical data accuracy and completeness Applying query resolution techniques and providing guidance to site staff Managing investigational product inventory, reconciliation, and storage and security Reviewing the Investigator Site File and Trial Master File for accuracy and completeness Documenting activities and supporting subject/patient recruitment, retention, and awareness strategies Understanding project scope, budgets, and timelines, and managing site-level activities to meet project objectives Acting as a primary liaison with study site personnel and attending investigator meetings and sponsor face-to-face meetings Providing guidance on audit readiness standards and supporting preparation for audits The ideal candidate will have: A Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements Excellent communication, presentation, and interpersonal skills Ability to manage required travel of up to 75% on a regular basis Syneos Health offers a range of benefits, including career development and progression opportunities, supportive and engaged line management, technical and therapeutic area training, peer recognition, and total rewards programs. Job Data by YubHub .