Accountabilities:
































In collaboration with the global study team and key vendors, you'll support clinical study execution, ensuring adherence to timelines and quality standards.

- Lead the preparation of study documents and vendor-related documents, such as the Vendor Oversight Plan.

- Facilitate interactions with cross-functional team members, including Data Management, Procurement, Regulatory, Patient Safety, and Quality Assurance.

- Collaborate closely with partners to execute delegated aspects of the clinical study, aligning with objectives set by the GPD, GSAD, or GSM.

- Contribute to planning and execution of internal and external meetings.

- Identify risks and issues, developing mitigation and action plans.

- Support GSM in project and budget management.

- Participate in or lead departmental initiatives and SME functions.

- Mentor team members, promoting professional development and collaboration.

- Provide support for other study and functional activities as assigned.

Essential Skills/Experience:

- Certificate of Disability equal or superior to 33%.

- Bachelor’s degree or equivalent in clinical practice/health care, life sciences, or drug development, or commensurate work experience.

- Proficiency with technological systems (Microsoft Office such as: Excel, PowerPoint, and SharePoint Online, eTMF and Veeva Systems).

- Excellent organizational communication and time management skills.

- Highly proactive and willing to take initiative.

- Strong relationship building skills.

- Ability to use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during sta