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Medical Monitor (Internal Medicine)

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Entry-level / graduate
Work from: 

Offer summary

Qualifications:

Medical Doctor degree, Internal Medicine certification, Minimum 10 years medical practice experience, Prior clinical trial experience is a plus, Full working proficiency in English and Portuguese.

Key responsabilities:

  • Advise on medical matters for clinical studies
  • Collaborate on clinical development documents
  • Review clinical data for participant safety
  • Address safety issues and ensure compliance
  • Organize clinical advisory boards and monitor risks
PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large https://www.psi-cro.com/
1001 - 5000 Employees
See more PSI CRO AG offers

Job description

Company Description

PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.

Home-Based in Brazil

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 organize and lead clinical development advisory boards and safety monitoring boards
  • Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines
  • Review and sign off clinical documents with respect to medical relevance.

Qualifications
  • Medical Doctor degree
  • Internal Medicine certification is a must
  • Prior and wide experience in medical practice/patient care (minimum of 10 years)
  • Prior experience working with clinical trials is a plus
  • Prior experience with ICU is a plus
  • Full working proficiency in English and Portuguese
  • Proficiency with MS Office applications
  • Communication, presentation and analytical skills
  • Problem-solving, team and detail-oriented

Additional Information

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.

Required profile

Experience

Level of experience: Entry-level / graduate
Industry :
Pharmaceuticals
Spoken language(s):
EnglishEnglishPortuguese
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Problem Solving
  • Analytical Skills
  • Teamwork
  • Detail Oriented
  • Microsoft Office

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