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Psicro

Psicro

Medical Monitor

Company

Psicro

Role

Medical Monitor

Job type

Full-time

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Salary

Not disclosed by employer

Job description

s 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.

Full-time employment based in Singapore

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
  • 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
  • Medical Doctor degree
  • Board-certification in major therapeutic area (Oncology, Infectious disease, Gastroenterology, Hematology, Internal Medicine) is desirable 
  • Prior experience in Clinical Research.
  • Familiar and comfortable with clinical concepts, practices and local regulations regarding clinical research trials experience with local health authority 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 organization
  • Must possess excellent leadership, communication, presentation, and organizational 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

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

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