We are looking for Medical Monitor to join our MedSci Consulting and Excellence group.
Medical Monitor (MM) provides medical expertise and oversight for the entire clinical trial, from initial study design through final study close-out.
Main responsibilities:
- Develop and update medical monitoring SOPs
- Develop and update study-specific Medical Monitoring Plan
- Consult involved personnel in medical issues during study design development and study protocol writing
- Review applicable study documents (Study Protocol and Protocol Amendments, IB, CRF, Final Study Report, Safety Management Plan, relevant project instructions, etc.)
- Consult investigators, Sponsor and OCT team in medical issues throughout the study (regarding AE and other safety events or concerns, eligibility criteria, dosing, and other relevant questions)
- Assist in pharmacovigilance activities
- Attend project related meetings and trainings (including Investigator’s Meetings)
- Provide therapeutic and relevant project specific trainings
- Liaise with Key Opinion Leaders, Data Monitoring Committees and other relevant parties involved in the study
- Review subject targeted data according to Medical Monitoring Plan
- Participate in Data Review Meetings
- Provide input on medical topics for Question-and-Answer Logs and Newsletters, as needed
Requirements:
- MD or Pharm D degree
- At least 3 years of clinical research experience
- At least 1 year of experience as a medical advisor or medical monitor
- Experience in oncology projects is a plus
- Medical practitioner experience is preferred
- Advanced English, both written and spoken
We offer:
- Challenging job in a highly qualified team
- Employee-friendly work environment
- Competitive salary
- Professional growth in clinical research field
If you want a career that makes a difference, then you are the person we’ve been looking for and OCT is the place for you!
Apply today!
