
Medical Development Specialist
2 semanas atrás
Job Overview
- We are seeking a skilled expert to provide clinical guidance on study designs and trial feasibility.
- The ideal candidate will drive fast and high-quality trial site start-up through expert input during planning phases.
- Responsibilities include providing clinical expertise for IRB/EC interactions and informed consent content.
- Developing trial plans that address recruitment challenges and ensure data quality.
- Delivering robust training on indications, compounds, and protocols to internal and external stakeholders.
- Leading clinical recruitment strategies using physician insights and patient engagement.
- Supporting regulatory inspections and audits with scientific and clinical expertise.
- Ensuring adherence to safety standards and providing medical input on adverse events.
Requirements
- Advanced scientific degree is required.
- Strong understanding of clinical development processes and ICH/GCP guidelines is necessary.
- A minimum of 3 years of experience in clinical development or clinical practice is required.
- Proven ability to lead cross-functional teams and resolve complex clinical issues is expected.
- Excellent communication skills in English are a must.
Benefits
Our company culture is built around collaboration, diversity and inclusion, and innovation. We encourage our employees to take ownership of their work and contribute to the growth and success of the organization.
At our organization, we believe that helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other.
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