Clinical Research Associate - BioPharmaceutical (Yearly Contract)
ประกาศจากแหล่งภายนอกคุณสมัครได้โดยตรง — เราจะพาคุณไปยังหน้าสมัครงานของบริษัท ไม่ต้องสมัครสมาชิก ไม่มีคนกลาง ไม่ต้องล็อกอิน ThaiJobz
รายละเอียดงาน
Key Responsibilities
- Ensures the processes for Study Delivery are executed through the development of study reports tools, facilitation of the study delivery system and maintenance of the system
- As an expert, ensures delivery of a centrally managed study management service across clinical studies from start up to reporting
- Serve as main contact and works closely with the Document Management group until the Clinical Study Report is finalised
- Initiates and maintains production of study documents, ensuring template and version compliance
- Creates or imports clinical-regulatory documents into the Global Electronic Library according to the Global Document List
- Interfaces with Data Management Centre or Data Management Enablement representatives to facilitate the delivery of study related documents
- Manages and coordinates tracking of study materials and equipment
- Monitors administrative tasks during the study process, audits and regulatory inspections, according to company policies
- Acts as a technical owner within Patient Safety with a deep understanding of processes and internal regulations
- Keeps own knowledge of best practices and new relevant developments up to date
- Liaises with compliance team members to improve regulatory processes within the team
- Identifies opportunities to improve the methodology and provide practical solutions for clinical development
Qualifications
- Essential: Bachelor's degree in relevant discipline
- Experience of Study Management within a pharmaceutical or clinical background
- Knowledge of relevant legislation and new developments in the area of Clinical Development and Study Management
- Desirable: Advanced degree within the field
- Professional certification
- Understanding of multiple aspects within Study Management
Key Relationships
- Internal: Study management function; Other AstraZeneca employees
- External: External service providers and regulatory bodies
About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world's most serious diseases. At AstraZeneca, we're dedicated to being a Great Place to Work where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.
คุณสมบัติผู้สมัคร
- ประสบการณ์
- 3-5 ปี
- การศึกษา
- ไม่ระบุ
