Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Opportunity for career advancement and growth within a leading clinical research organization
- Competitive salary with a range of additional benefits focused on well-being and work-life balance
- Access to a global network of health professionals through the Employee Assistance Programme
- Flexible benefits including childcare vouchers, gym memberships, and health assessments
- Supportive and inclusive work environment that values diversity and equal opportunity
- Engaging role with the potential to make a significant impact on clinical trial processes

What to Expect (Job Responsibilities):
- Provide subject matter expertise in creating timelines using integrated study timeline templates
- Attend study execution team meetings to support timeline-related activities
- Coordinate cross-functional discussions for timeline customization and maintenance
- Monitor project progress and identify potential delays or roadblocks
- Develop and maintain templates and tools related to global timeline management

What is Required (Qualifications):
- Bachelor’s Degree or international equivalent required; Life Sciences preferred
- Knowledge of global regulatory and compliance requirements for clinical research
- Demonstrated experience in project/program management and matrix leadership
- Excellent communication, teamwork, and problem-solving skills
- Proficient in Microsoft Suite, including MS Project and SharePoint

How to Stand Out (Preferred Qualifications):
- Experience managing multiple studies concurrently
- Fluent business English (oral and written)
- Knowledge of local country regulatory requirements in clinical research

#ClinicalResearch #ProjectManagement #CareerOpportunity #DiversityAndInclusion #WorkLifeBalance

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