Clinical Research Medical Advisor

3 semanas atrás

São Paulo, São Paulo, Brasil Healthcare Businesswomen's Association Tempo inteiro

Job Description Summary

Location: São Paulo, Brazil
Relocation Support: Yes
Step into a role where your clinical expertise can truly shape the future of medicine. As a Clinical Research Medical Advisor at Novartis, you'll be at the forefront of driving high-quality clinical trials, ensuring scientific excellence, and accelerating access to innovative treatments. You'll collaborate with cross-functional teams, external experts, and trial sites to bring impactful therapies to patients faster. This is your opportunity to influence trial strategy, enhance patient engagement, and contribute meaningfully to global health outcomes—all while growing your career in a dynamic, purpose-driven environment.

Job Description

Key Responsibilities

  • Validate study designs and assess trial feasibility based on clinical practice and competitive analysis.
  • Drive fast and high-quality trial site start-up through expert input during planning phases.
  • Provide clinical expertise for IRB/EC interactions and informed consent content.
  • Develop trial plans that address recruitment challenges and ensure data quality.
  • Deliver robust training on indications, compounds, and protocols to internal and external stakeholders.
  • Lead clinical recruitment strategies using physician insights and patient engagement.
  • Support regulatory inspections and audits with scientific and clinical expertise.
  • Ensure adherence to safety standards and provide medical input on adverse events.

Essential Requirements

  • Advanced scientific degree (M.D. highly preferred; Ph.D. or Pharm.D. also considered).
  • Strong understanding of clinical development processes and ICH/GCP guidelines.
  • Minimum 3 years of experience in clinical development or clinical practice.
  • Proven ability to lead cross-functional teams and resolve complex clinical issues.
  • Excellent communication skills in English and the local language.
  • Ability to deliver high-quality presentations and adapt across therapeutic areas.

Desirable Requirements

  • Subspecialty training or experience with Real World Evidence (RWE).
  • Familiarity with innovative study designs and data sources such as registries or electronic health records.

Skills Desired

Clinical Monitoring, Clinical Research, Clinical Trial Protocol, Clinical Trials, Decision Making Skills, Drug Development, Health Sciences, Lifesciences, Regulatory Compliance #J-18808-Ljbffr

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