临床医师(外派) Clinical Research Physician

• Takes medical responsibilities to ensures successful conduct and integrity of all in-scope clinical studies.
• Work as China study physician in China-join global studies or under the supervision from study lead global physicians.
• Contributes to study design and develops appropriate protocol synopsis and protocols/amendments to match China clinical practice and meet regulatory requirement.
• Provides medical monitoring for the trials to review medical data, support to evaluate AEs/SAEs and detect safety signals, to ensure the data with high quality and the safety of participants.
• Supports document preparations for China regulatory filing and registration as a clinical science expert.
• Provides support on the consultation to clinical operation colleagues on protocol design questions and answering protocol related questions from site investigators as a clinical science physician.
• Keeps close connection with global study team during the entire course of the study.
• Coordinates the collection and analysis of clinical data for internal analysis and review.
• Prepares presentations for scientific conferences as well as for clinical study investigator meetings and expert advisory meetings. Develops manuscripts for publication in peer reviewed journals.
• Responsible for interacting and communicating with China KOLs for China development plan and protocol design.
• Coach colleague internally and externally as needed.
• Prelaunch support in this TA.
• Maintains up-to-date medical/scientific knowledge as well as clinical trial landscape and competitive intelligences in the TA.
• Other tasks assigned by line manager as appropriate.

Education, Qualifications, Skills and Experience
Essential
• Master's degree in medical discipline or above
• Experience of management and design of clinical trials；
• Minimum 1 year of experience (only with MD/PhD) in drug development in top MNC or 2 years in medical practice or 2 years in industry related (MA).
Desirable
• PhD in scientific discipline
• Extensive general medical knowledge
• Extensive experience in managing or designing clinical trials
• Thorough knowledge of study analysis and design in all phases of drug development

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.iqvia.com