Global Study Leader (m/f/d)
Responsibilities
- Provides subject matter expertise on specific Clinical Operations activities either directly related to or in support of executing studies and/or enabling projects. Accountable for activities that contribute to the outcome of one or more studies and/or Clinical Operations enabling projects
- Identifies, contributes to, and participates in continuous improvement and change management activities to solve complex problems and bring new perspectives to existing solutions in support of diagnostics solutions and/or enabling projects
- Independently and with minimal guidance develops plans, creates and manages budgets, and ensures the consistency of studies and/or projects that support studies
- Collaborates across Clinical Operations and other functions to develop and implement best practices across Clinical Operations
- Understands, applies good knowledge of applicable standards and regulations (ICH-GCP, IVDD/IVDR, MDR, SaMD, FDA, NMPA regulations etc) in the review of studies and/or other associated projects
- Drive patient and customer-centricity (mindset, behaviors and actions) by always putting the needs of patients and the customers first
- Partner across diverse regions, cultures, and time zones to create an environment of belonging, inclusion and diversity
- Demonstrate flexibility and adaptability to perform in a fast-paced, matrixed environment where fluid, cross-team collaboration is crucial. Leverage excellent verbal and written communication skills
- Works closely with Medical Affairs in cross-functional collaboration (e.g. with Regulatory Affairs, R&D, Clinical Operations teams) to support global strategies and planning of timeline and costs. Drives process improvements, harmonization and evolution of processes and templates
- Oversees planning and operational aspects of Investigator Initiated Studies and Research Collaborations as well as accountable for study-level budget of assigned studies
Profile
- Minimum of bachelors degree in Life Science and/or relevant expertise in the Healthcare Industry or a related field
- First experience in study management or clinical project management
- Conceptual and practical knowledge of Clinical Operations or related areas
- Knowledge of best practices and the role of Clinical Operations in product development; aware of Roche´s place in the market and our value proposition to patients and customers
- Solves complex problems; takes a new perspective on existing solutions; exercises judgment based on the analysis of multiple sources of information
- IT affinity for applications such as GSuite
- Fluency in English
Benefits
- You will work in an international environment
- A very renowned company
About Hays
As one of the largest recruitment agencies on the legal market, Hays ranks as a first stop for legal experts who have set high goals for their careers and are able to achieve them. This applies just as equally to committed "newcomers" as it does to experienced solicitors and attorneys who want to transition to a law firm or corporate environment. Since 1991, Hays has offered personnel consulting and recruitment services for legal professionals. Our consultants are highly experienced in their domain and are aware of the fine details and distinctions that can make the difference between signing on the dotted line or having your application rejected. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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