Medical Monitor

Alimentiv; Berlin; On-site; EUR 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in Berlin is looking for a medical professional to provide guidance on clinical protocols and ensure compliance during studies. Responsibilities include reviewing study materials, supporting safety management, and collaborating effectively with internal teams. Candidates should have a strong background in medical oversight within clinical settings.

Qualifications

• Experience in providing medical guidance in clinical settings.
• Ability to communicate effectively with cross-functional teams.
• Familiarity with clinical trial protocols and medical oversight.

Responsibilities

• Provide unbiased medical guidance to clinical sites and study teams.
• Assure protocol compliance and medical congruency.
• Review critical study materials and assist in writing final reports.

Job description

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