医学经理-肿瘤 (MJ001265)-全国
1天前
Chengdu, Sichuan, 中国
ClinChoice昆翎
全职
¥18,000 - ¥25,000 临时
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该职位来源于猎聘 Primary
Responsibilities:
• Develop product clinical development strategy and executive plan under appropriate departmental supervision.
• Skilled in organizing and writing materials related to medical clinical trials of CDE communication meetings, attending face-to-face meetings and communicating with CDE experts when necessary.
• Establish good communication relationship with medical experts in key fields, and close communication about research programs.
• Draft, review, and QC of clinical documents to ensure compliance of documentation to GCP, SOPs.
• Development medical supervision plan and function as a medical monitor in case of need, to ensure the quality and safety of the project, including but not limited to the monitoring of SAE and programme deviation.
• Work closely with CO, RA, BD, PV and other departments, provide advice, support and assistance according to project needs (select of leading PI/ Participate in project meetings and protocol discussion).
• Serve as primary technical contact with client under appropriate departmental supervision.
• Provide medical professional guidance to subordinates.
• Other activities/tasks assigned by supervisor. 任职要求 Qualification
• Ph.
D. in Medical Science, More than 1 years clinical experience in oncology or chronic disease therapeutic area.
• Or master degree major in medical science, More than 3 years clinical experience in oncology or chronic disease therapeutic area.
• Or bachelor degree in medicine, More than 5 years clinical experience in oncology or chronic disease therapeutic area.
• Be familiar with the key points of clinical trials and relevant policies and regulations.
• Languages: Excellent written and read English Excellent oral English are preferred.
Responsibilities:
• Develop product clinical development strategy and executive plan under appropriate departmental supervision.
• Skilled in organizing and writing materials related to medical clinical trials of CDE communication meetings, attending face-to-face meetings and communicating with CDE experts when necessary.
• Establish good communication relationship with medical experts in key fields, and close communication about research programs.
• Draft, review, and QC of clinical documents to ensure compliance of documentation to GCP, SOPs.
• Development medical supervision plan and function as a medical monitor in case of need, to ensure the quality and safety of the project, including but not limited to the monitoring of SAE and programme deviation.
• Work closely with CO, RA, BD, PV and other departments, provide advice, support and assistance according to project needs (select of leading PI/ Participate in project meetings and protocol discussion).
• Serve as primary technical contact with client under appropriate departmental supervision.
• Provide medical professional guidance to subordinates.
• Other activities/tasks assigned by supervisor. 任职要求 Qualification
• Ph.
D. in Medical Science, More than 1 years clinical experience in oncology or chronic disease therapeutic area.
• Or master degree major in medical science, More than 3 years clinical experience in oncology or chronic disease therapeutic area.
• Or bachelor degree in medicine, More than 5 years clinical experience in oncology or chronic disease therapeutic area.
• Be familiar with the key points of clinical trials and relevant policies and regulations.
• Languages: Excellent written and read English Excellent oral English are preferred.