Leader in Clinical Research Excellence

1 dia atrás

São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro US$90.000 - US$120.000
Medical Advisor in Clinical Research

We are seeking a highly skilled Medical Advisor to join our team. As a key member of our clinical research department, you will be responsible for overseeing the execution and interpretation of clinical trial investigations, data collection activities, and clinical operations.

Your primary focus will be on establishing and approving scientific methods for design and implementation of clinical protocols, data collection systems, and final reports. You will also assist in new and ongoing clinical research and trials, ensuring efficiency and timely processing of confidentiality agreements and clinical agreements.

In this role, you will supervise protocol compliance and study closure, manage clinical and regulatory files, and maintain the clinical inventory for distribution to research sites. Additionally, you will interface with study sites, clinical investigators, CROs, and other vendors, selecting, developing, and evaluating personnel to ensure efficient operation of the function.

Key Responsibilities:
  • Validate study designs and assess trial feasibility based on clinical practice and competitive analysis.
  • Drive rapid, high-quality initiation of research centers through specialized contributions in planning phases.
  • Provide clinical expertise for interactions with Ethics Committees (IRB/EC) and informed consent language.
  • Develop study plans addressing recruitment challenges and ensuring data quality.
  • Provide robust training on indications, compounds, and protocols for internal and external stakeholders.
  • Lead clinical recruitment strategies using medical insights and patient engagement.
  • Support regulatory inspections and audits with scientific and clinical knowledge.
  • Ensure safety standards compliance and provide medical opinion on adverse events.
Requirements:
  • Advanced scientific degree (MD highly preferred; PhD or PharmD 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 written and spoken English communication.
  • Ability to deliver high-quality presentations and adapt to different therapeutic areas.
Skills and Qualifications:

Health sciences, Clinical Monitoring, Clinical Trial Protocol, Regulatory Compliance, Decision Making, Drug Development, Clinical Trials, Lifesciences, Clinical Research

Why Join Us: We offer a collaborative environment where talented professionals like you can thrive. By combining your skills and expertise, we aim to achieve breakthroughs that change patients' lives. Ready to make a difference?

Talent Community: If this role isn't right for you, sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up.

Employment Details:
  • Seniority level: Mid-Senior level
  • Employment type: Full-time
  • Job function: Health Care Provider
  • Industries: Pharmaceutical Manufacturing

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