The Senior Data Manager reports to the Data Manager Project Coordinator, serve as primary point of contact to the study team for clinical data related matters and ensure clinical data are managed in compliance with applicable standards, regulatory guidelines and OPIS SOPs. Ensure data is managed in compliance with applicable standards (e.g., CDISC), regulatory guidelines and OPIS SOPs Prepare/validate Data Management documents (CRF, Data Management Plan, Data transfer specifications, etc.) Design/validate the paper and/or electronic Case Report Forms (CRF), including paper PROs (diaries, questionnaires), in co-operation with the Sponsor, and the study team Prepare/validate the eCRF/clinical databases and related tools Prepare and manage change request of database Perform data cleaning activities Perform coding activities of medications and medical terms using medical dictionaries Perform SAE reconciliation when required Manage database lock and freeze before data analysis Prepare, maintain, and archive data management documentation Perform quality controls according to the Data Management Plan Liaise with Sponsor and external stakeholders regarding data management activities Escalate potential risks/issues to Direct Manager Track activities and milestones to ensure timely project deliverables Participate to meetings, kick-off meeting and teleconferences for assigned projects Organize/perform trainings for project team - Collaborate in establishing and maintaining SOPs related to Data Management Promote the introduction of digital technologies and innovative data processing tools and acts as a mentor for junior staff Perform and complete on time all required trainings (study trainings, training on OPIS and/or Sponsor SOPs, all other applicable trainings) by the assigned due date Bachelor’s degree Solid knowledge of ICH-GCP/ISO14155, clinical data management and HA requirements pertaining to pharmaceutical research and specifically to Data Management Digital skills and good knowledge of FDA 21 CFR Part 11 and system validation Solid knowledge on relational databases and programming languages Knowledge of SAS system is a plus Excellent knowledge about Microsoft package Strong commitment to quality English language (fluent reading, writing and verbal skills) Planning and organizational skills Founded in 1998 in Italy and now operating at an international level, OPIS is a full-service science driven biotech focused CRO providing premium trial management for multi-country clinical trials, including state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know-how and experience to guarantee a top-quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.) Please read the information notice on the processing of personal data in the candidates information section of our company website.