... achieve their goals. The Senior Clinical Research Associate will function operationally ... : Monitor on-site and remotely clinical trials in accordance with TFS ... . Possess the understanding of Good Clinical Practice regulations, ICH guidelines. Ability ...
... specializing in Patient Recruitment for Clinical Trials to lead and oversee patient recruitment strategies across multiple clinical studies. In this role, you ... with Stakeholders: Work closely with clinical operations, study sponsors, CROs, site ...
... for a highly committed Senior Clinical Marketing Specialist (d f m) ... Maastricht (Netherlands). As a Senior Clinical Marketing Specialist at Abiomed within ... accurate marketing materials, including brochures, clinical dossiers, white papers, and other ...
... for a highly committed Senior Clinical Marketing Specialist (d f m) ... Maastricht (Netherlands). As a Senior Clinical Marketing Specialist at Abiomed within ... accurate marketing materials, including brochures, clinical dossiers, white papers, and other ...
... team in Global Clinical Science and grow with exciting challenges As a member of our clinical team you shape the growth ... options Driving clinical and medical negotiations with Ethics ... of experience in clinical research and development, preferably in ...
... - mit dem Konzept der LEADING NURSE. Wir gewährleisten trotz des Fachkräftemangels ... mit dem Konzept der LEADING NURSE bereits die Pflegeorganisation der Zukunft ... . Neugierig? Werden Sie als LEADING NURSE fachliche Leitung und planen, steuern ...
... , and close-out visits for clinical trials. Ensuring protocol compliance, data ... years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH- ...
... , and close-out visits for clinical trials. Ensuring protocol compliance, data ... years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH- ...
... , and close-out visits for clinical trials. Ensuring protocol compliance, data ... years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH- ...
... , and close-out visits for clinical trials. Ensuring protocol compliance, data ... years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH- ...