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Senior Medical Advisor
2 semanas atrás
Clinical research medical advisors play a vital role in supervising and executing clinical trial investigations, data collection activities, and clinical operations. They establish and approve scientific methods for designing and implementing clinical protocols, data collection systems, and final reports.
Key Responsibilities:- Validating study designs and assessing trial feasibility based on clinical practice and competitive analysis.
- Driving rapid, high-quality initiation of research centers through specialized contributions in planning phases.
- Providing clinical expertise for interactions with Ethics Committees (IRB/EC) and informed consent language.
- Developing study plans addressing recruitment challenges and ensuring data quality.
- Providing robust training on indications, compounds, and protocols for internal and external stakeholders.
- Leading clinical recruitment strategies using medical insights and patient engagement.
- Supporting regulatory inspections and audits with scientific and clinical knowledge.
- Ensuring safety standards compliance and providing medical opinion on adverse events.
- An advanced scientific degree such as an MD, PhD, or PharmD.
- A strong understanding of clinical development processes and ICH/GCP guidelines.
- A minimum of 3 years of experience in clinical development or clinical practice.
- The ability to lead cross-functional teams and resolve complex clinical issues.
- Excellent written and spoken English communication skills.
- The capacity to deliver high-quality presentations and adapt to different therapeutic areas.
- Subspecialty training or Real-World Evidence (RWE) experience.
- Familiarity with innovative study designs and data sources such as registries or electronic health records.
Health sciences, Clinical Monitoring, Clinical Trial Protocol, Regulatory Compliance, Decision Making, Drug Development, Clinical Trials, Lifesciences, Clinical Research
