Global Study Leader
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An innovative company, which is a subsidary of a leading pharmaceutical company, is seeking a Global Study Leader to join their team in Shanghai, China
Role Responsibilities:
- Lead and manage a cross clinical delivery sub team to operationally deliver defined clinical studies or clinical project activities to time, cost and appropriate quality.
- Lead the operational delivery of clinical studies, via a team of contributing experts from the study specification to the final clinical study report and archived master file.
- Provide input into study feasibility and study specifications, and produce essential documents including the authoring of clinical study protocols across both interventional and non-interventional studies.
- When working across studies or project work package ensures consistency across the development program.
- To be the interface to partners and oversee the delivery to plan of studies performed through external partners (such as Alliance partners, CROs, vendors and Academic Research Organizations) and to monitor progress, identify and solve operational issues.
- Lead/contribute to clinical submission assembly, regulatory response and payer evidence teams and contributes to advisory board and steering committee meetings.
- Management of changes to project scope and costs (including CRO and other vendors change orders) and reporting project status by participating in project planning and control activities and generation of status reports as required.
- Accountable for agreeing with the project team and functions the most efficient procedures to support delivery by taking the project situation and compliance requirements into account.
Role Requirements:
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research. Advanced degree is preferred.
- At least 5 years' experience from within the pharmaceutical industry or similar organization or academic experience.
- Extensive knowledge of clinical operations, project management and processes
- Good experience of clinical development/drug development process in various phases of development and therapy areas.
- Project management certification is desirable but not mandatory.
- Evidence of developing partnering skills
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Stephen Qin on +86 21 5169 4107 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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