Base pay range
In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training, medical guidance on protocol compliance, ensuring medical congruency at subject and study level and oversight of coding of medical terms. You will be responsible for supporting clinical safety, project, and data management by reviewing critical study materials at study start up stage and data listings through the study duration. You may also assist with reviewing the interim or final data sets and the writing of the final study report. Day to day you will be in regular communication with the medical team (including medical teleconferences), and interfacing with the internal cross functional teams as well as sponsor medical groups throughout the study.
Medical Oversight
- Provide clarity on general protocol questions, and medical guidance for protocols as required
- Serve as medical expert providing guidance on patient eligibility, and investigational product related questions
- Document contacts in accordance with Alimentiv or study specific procedures
- Consult with Alimentiv Medical Director(s), Sponsor Medical group and/or Safety about medical questions pertaining to the indication/compound under study
- Observe and identify safety issues and other trends as
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Medical Monitor in Berlin Arbeitgeber: Alimentiv
Als Arbeitgeber im Bereich klinisches Datenmanagement bieten wir eine dynamische und unterstützende Arbeitsumgebung, die auf Teamarbeit und kontinuierliche Verbesserung ausgerichtet ist. Unsere Mitarbeiter profitieren von umfangreichen Weiterbildungsmöglichkeiten, einem formellen Mentorenprogramm und einem leistungsbasierten Bonusprogramm, das ihre Erfolge anerkennt. Darüber hinaus fördern wir eine positive Unternehmenskultur, die auf Zusammenarbeit und Innovation abzielt, und bieten wettbewerbsfähige Vergütungspakete, die auf die regionalen Gegebenheiten abgestimmt sind.
