Need advice on clinical trials and study designs

Seeking an experienced professional in clinical research to provide strategic and technical guidance on clinical trial design, registry studies, and real-world evidence (RWE) generation. This role will support the development of evidence strategies in post-marketing phase after the drug is approved. Key Responsibilities Provide expert input on clinical trial design, including protocol development, endpoints, and statistical considerations Advise on the design, implementation, and optimization of patient registries and observational studies Guide real-world evidence (RWE) strategy, Review and provide input on study protocols and publications Identify innovative approaches to evidence generation, including hybrid and pragmatic trial designs Qualifications & Experience Demonstrated expertise in clinical trial methodology, observational research, and RWE generation Experience with registry design and management Proven track record of publications or successful regulatory submissions is a plus Key Skills Ability to translate scientific concepts into actionable strategies Shape evidence generation strategies for innovative therapies How to Apply Please submit your CV and a brief summary of relevant experience in clinical trial design, registry studies, and RWE.