Project Manager

Susan is working as a centralised monitoring manager, she is currently on leave from August 2021. In the past, her primary area of work has been in clinical research. In her previous position she managed part of the central team, worked on new data monitoring methods, real data collected from patients, data management, further participated in processes and also trained the international team. In the future she would like to work in a new area like IT, she is interested in positions like IT manager and Project manager. The candidate has English at C1 level so in the future she would prefer to work where she would work in an English team.

Centralized Monitoring Manager

December 2015 - August 2021

• Managed clinical deliverables for assigned clinical studies/programs, ensuring adherence to protocols, SOPs, regulations, and project plans.
• Led project/program deliverables for specific customers and projects.
• Oversaw global studies and centralized monitoring services on multiple studies.
• Contributed to study-specific document development and implemented study/program analytics strategies.
• Managed project resources and provided inputs for continuous process improvements.

Clinical Research Associate 3

February 2014 - November 2015

• Monitored clinical trials in Slovakia and Czech Republic.
• Ensured compliance with study protocols and regulatory requirements.
• Conducted site visits and performed data collection and verification.
• Collaborated with study teams and investigators to address issues and ensure study integrity.
• Managed study documentation and reported findings.

Sr. Clinical Research Associate

September 2010 - January 2014

• Monitored clinical trials in Slovakia, ensuring protocol compliance and data integrity.
• Conducted site visits, performed source data verification, and resolved study-related issues.
• Collaborated with study teams and investigators to ensure study quality and adherence to regulations.
• Managed study documentation and maintained accurate records.
• Contributed to study start-up activities and feasibility assessments.

Start-up Manager

March 2010 - August 2010

• Conducted feasibility assessments for clinical trials in Slovakia.
• Managed site selection activities and communicated with regulatory authorities and ethics committees.
• Assisted in study start-up activities and ensured compliance with regulatory requirements.
• Coordinated with internal and external stakeholders to facilitate smooth study initiation.
• Contributed to site selection strategies and provided support in the selection process.

Clinical Research Associate

January 2007 - August 2010

• Monitored clinical trials in Slovakia, ensuring compliance with protocols and regulations.
• Conducted site visits, performed data collection and verification, and resolved study-related issues.
• Collaborated with study teams and investigators to ensure study quality and data integrity.
• Managed study documentation and maintained accurate records.
• Assisted in study start-up activities and contributed to protocol development.

Note: The CV does not mention company names, so the roles are presented without specifying the companies.