Syneos FSP COS 临床试验助理 - Shanghai

Thispositionisresponsibleforassistingclinicalresearchteamsineffectivelyconductingclinicalresearchstudiesbyprovidingadministrationandprojecttracking. · ...

This position is responsible for managing TMF/eTMF in accordance with applicable regulations and guidelines. · ...

The job involves managing clinical trial documents, assisting in the implementation of clinical trials, and performing administrative tasks. The role requires a bachelor's degree in pharmacy/nursing or other life sciences and strong communication skills.Manage TMF/eTMF in accorda ...

This position provides clerical administrative and technical support to one or more business units or clients within Clinical Operations. · Perform activities in compliance with Corporate and Clinical Operations Policies Standard Operating Procedures and Work Instructions. · Assi ...

Job Summary: The position provides clerical, administrative and technical support to business units or clients within Clinical Operations. · Responsibilities: Perform activities according to Corporate and Clinical Operations Policies; assist with site management activities includ ...

The position is responsible for providing clerical, · administrative, and technical administrative support to one or more business units · or clients within Clinical Operations.Candidates familiar with VBA or other automation · technical skills (such as Power Apps, · Power Automa ...

This position is from the recruitment website Hire Ø Bachelor's degree required. Preference to candidates with a clinical medicine or nursing, pharmacy degree Ø 3-5 years working experience in pharmaceutical industry Ø Must have good organization skills, be a team player, functio ...

The clinician will lead clinical study teams and work collaboratively with other study team members to ensure the success of clinical trials. · Co-chairs clinical study team and works collaboratively with other study team members. · Provides clinical and scientific expertise to t ...

Clinician leads clinical study team and works collaboratively with other study team members. Point of accountability to the BU for design, conduct, interpretation and reporting of one or more clinical studies (or elements of those studies). · ...

The Clinical Trial Administrator (CTA) is responsible for performing a variety of research, database, and clerical duties of a complex and technical nature in support of multiple clinical trials. · This position also provides administrative support to clinical teams by reviewing ...

The Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials. · Typical duties will include supporting other members of the local study team, · collecting data required for regulatory submissions, · document tracking contracts financ ...

+The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. · +Perform activities in compliance with applicable Corporate and Clinical Operations Policies, Standard ...

The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. · Bachelor degree or above · Good communication and interpersonal skills · Ability to embrace new technolo ...

The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. · ...

The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. · ...

该职位来源于猎聘此岗位外资Biotech要求1年及以上CTA经验福利培训叠加享受CRO+申办方双重福利 · ...

· Job summary · , · , · bHabilidades: · ...

개에 FSP COS 총하을그와긄 · （ 1.） 2％-3）좋는 CTA선는의, 수월선는 GCP서합로 , · 4. Microsoft Office (찾 D,캔,기) , · 5. ( ) 6.％ ( ) 7.％ English workable <hr class=\ ...

该职位来源于猎聘 FSP Global Pharma · 熟悉并掌握临床试验合同的关键条款 · 审阅项目组往来邮件及合同 · 组织日常与法务团队协同开会就需法务介入的协议条款进行讨论等 · ...

协助项目经理完成临床试验项目支持工作 · 维护和更新临床项目的信息 · 跟进项目进度确保符合计划 · ...