Our clients lead asset is treating aggressive forms of cancer through a novel immunotherapy approach. The company is highly innovative and their technology adopts a versatile approach which is highly effective and has seen success in current patient populations.
Executing clinical development and protocol implementation of key programs.
Duties of the role:
Work cross functionally with clinical, medical and other internal departments
Ensuring proper data collection, analysis and presentation of key trial insights
Contribute to protocol development
Generating regulatory documentation for submissions
Engage with health authorities and regulatory bodies
Provide scientific input for various publications
Actively support the internal research and development teams and contribute to pipeline development
Qualifications and skills required for the role:
MD with 2 – 3 years of relevant industry experience
Oncology experience is advantageous
Highly experienced with protocol design, implementation and development
Exceptional ability to train and educate medical and clinical teams
Excellent knowledge of ICG-GCP guidelines as well as local and international regulations
Ability to interpret analyse and present complicated clinical trial data
Exceptional communication skills and ability to adapt language on an interdisciplinary team
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