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水平: Associate
工作类型: Full-time
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工作内容
- Salary: up to 103 CHF ph (all incl)
- REF Number: 00051714
- Consultant: Jocelyn Blackham
- Contact: 0041 (0) 800 106 106
- Date Published: 21.09.2021
- Sector: Basel Area
- Location: PRATTELN, Experienced, Senior/Team Leader
- Discipline: Clinical - Clinical Operations
The key responsibilities of the Senior Clinical Trial Scientist will include:
- Developing a soundunderstanding of the science and medicine related to an indication and trial and performing literature searches as needed to keep knowledge up to date
- Managing deliverables such as clinical trial protocol and related documents such as the ICF, study committee charters, study guidelines/instructions, PD code list, subject narratives, and the CSR
- Providing input into and reviews cross-functional trial documents such as the SAP, ESP requirements and specifications, monitoring guidelines, data review manual
- Participating in discussions with external experts
- Performing data review and medical monitoring during the conduct of the trial
- Providing scientific input into responses for IRBs/ECs and HAs
- Coordinating/managing the study committees
- PhD, Pharm D, MSc or equivalent university degree in life or health sciences
- Previous experience in working experience in clinical development, in a contract research organization (CRO) or pharmaceutical company
- Experience/Knowledge in the filed of kidney diseases and/or autoimmune diseases is desirable
- Previous experience in either the planning, set-up, conduct, closing, and reporting of phase II and III clinical studies from a scientific perspective is an asset
- Previous experience in either the planning, set-up, conduct, closing, and reporting of phase II and III clinical studies from a scientific perspective (candidate with clinical trial experience is preferred) This is an excellent opportunity to join a growing pharmaceutical company.
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最后期限: 08-06-2024
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