2024-03-28
- 北京市||北京市||朝阳区
- 5-10年
- 硕士
- 全职
- 1
职位描述:
Main Responsibility:
Provides medical expertise on clinical drug development throughout life-cycle of compound:
•Supports study design, generation of study protocol, CRF, informed consent, Investigators Drug Brochure, Statistical Analysis Plan, and other study material.
•Provides continuous medical monitoring during study conduct, answers site questions on inclusion/exclusion criteria or other protocol questions, evaluates and assesses SAEs and AEs, reviews laboratory and other safety parameters, reviews patient profiles, reviews coded terms for medical history, concomitant medications, adverse events, and provides medical expertise to project teams during life-cycle of study.
•Provides therapeutic training relevant to specific study to the project team or site PI
•Attends and/or presents at investigator, internal and external project team meetings.
•Defines criteria for assesses and evaluates protocol deviations and recommends on actions to be taken. Assumes responsibility for ethical, e.g. medical, aspects of study.
•Contributes to discussions with health authorities, Ethics Committees, investigators, opinion leaders, internal and external clients.
•Supports BD in client contacts to discuss portfolio and development strategies
Qualification
•Master degree above, Medicine, Clinical is must.
•Fluently English is must.
•More than 5 years experiences in clinician or clinical R&D are must.
Personality:
•Positive attitude, drive to do your best, learning attitude
•Trustworthy and reliable for strong sense of responsibility and carefulness.
•patience and meticulousness is prefer.
我们致力于开发针对肿瘤耐药和转移的创新疗法
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电话: 025-58251030
邮箱: office@inxmed.com
公司地址: 南京市江北新区探秘路73号树屋十六栋D-2栋3层
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