[Hiring] Medical Monitor @PSI CRO

Role Description

As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.

Responsibilities:

• Advise clients, project teams, sites, data safety monitoring boards, regulatory agencies and third-party vendors on medical matters
• Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations
• Review and analysis of clinical data to ensure the safety of study participants in clinical studies
• Ensure that the reported data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
• Address safety issues across the study from sites and the study team
• Review listings for coded events to verify Medical Dictionary for Regulatory activities
• Participate in bid defense meetings
• Assist in Pharmacovigilance activities
• Identify Program risks, and create and implement mitigation strategies with Clinical Operations
• Ability to organise and lead clinical development advisory boards and safety monitoring boards
• Ensure Study team compliance with local regulatory agencies, ICH and GCP guidelines
• Review and sign off clinical documents with respect to medical relevance

Qualifications

• Medical Doctor degree, board certified/completed Fellowship in Internal Medicine
• Prior experience in clinical research/clinical trials
• Familiar and comfortable with clinical concepts, practices and local regulations regarding clinical research trials; experience with TGA interactions leading to drug approval strongly preferred
• Ability to interact with and train clinical monitors and physician investigators, and build constructive, trusting and respectful relationships with colleagues at all levels within and outside the organisation
• Must possess excellent leadership, communication, presentation, and organisational skills and be able to exercise sound critical thinking and problem-solving skills and execute position responsibilities with minimal guidance
• Proficiency with MS Office applications

Benefits

• Join our highly dedicated team of clinical research professionals with +250 Medical Doctors onboard
• Make a tangible difference within a professional and energetic organization founded by scientists