Contribute to trials' design and planning, collaborating for robust and scientifically sound protocols.
Oversee clinical trial execution, ensuring protocol adherence and compliance, collaborating with operations to monitor progress and address challenges effectively.
Analyze trial data, interpret results, and contribute to study reports. Collaborate with statisticians to ensure appropriate analysis methodologies are applied.
Aid in regulatory document preparation, including IND applications. Contribute to responses for queries and inspections.
Collaborate with teams and partners. Present trial updates at internal meetings and scientific conferences effectively.
Requirements:
Hold a degree or Master's in a relevant scientific field, bringing 3-10 years of clinical research experience.
Strong background in immunotherapy and a solid understanding of cancer biology.
Familiarity with regulatory requirements and guidelines for clinical trial conduct.
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