When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Key Accountabilities:
General Accountabilities
Accountable for building, forecasting and managing the Clinical Trial Budget
Leads the China core study team; manages, facilitates and documents core study team meetings (e.g. meeting agendas & minutes, action logs and decision logs) and facilitates effective decision making.
Ensures adequate China study team resources and leads study team chartering to ensure that study team structure, including sub-teams, are effective and efficient
Fosters optimal China study team health including formal team effectiveness assessments and action planning
Manages China study team communications to ensure cross-functional connectivity among study team members and supporting functional lines
Compliance with Parexel standards
Comply with required training curriculum.
Complete timesheets accurately as required.
Submit expense reports as required.
Update CV as required.
Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements
Strong Communication Skills
Demonstrated project management / leadership experience
Skills:
Broad experience in a Clinical Trial Execution discipline
Strong Communication Skills
Demonstrated project management / leadership experience
Knowledge and Experience:
Keen problem-solving skills.
Fluent in both oral and written English.
Fluent in host country language required.
At least 8 years in clinical practices
Education
Minimum of BS in relevant overall industry experience and at least one year in project management
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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