Do you recognize yourself in below skills & competences:
- Comprehensive Clinical Trial Knowledge: in-depth understanding of study designs, operational processes, and regulations.
- Organizational & Time Management Expertise: skilled in efficiently managing complex projects, balancing multiple priorities, and meeting deadlines.
- Effective Communication: skilled in conveying project goals, updates, and requirements to stakeholders, ensuring clarity and alignment.
- Strategic Problem-Solving and Decision-Making: ability to analyze situations and make informed, timely decisions to address challenges.
- Team Leadership & Motivation: proven track record of leading, motivating, and supporting project teams to achieve high performance and successful outcomes.
- Stakeholder Engagement & Relationship Building: expertise in building strong, collaborative relationships with clients, vendors, and cross-functional teams to ensure project success.
- Flexibility & Attention to Detail: adapting to changing situations while ensuring precision and adherence to applicable international standards.
- Self-Directed & Proactive: takes responsibility over projects, initiating actions with minimal guidance.
In this role, you will have the opportunity to:
- Lead the planning, execution, and management of clinical studies.
- Collaborate closely with cross-functional teams and external partners to achieve study deliverables.
- Proactively identify clinical project risks, provide input for appropriate countermeasures and contingency plans, and assure implementation of action plans to reduce project risks.
- Monitor and manage project timelines, budgets, and resources effectively while maintaining a focus on integrity, transparency, and accuracy in reporting.
- Together with the team, ensure that program requirements are met and clinical studies are executed in a compliant and scientifically appropriate manner.
- Be highly involved in clinical study planning and study design. Involvement includes study deliverables such as clinical protocol, monitoring plan, and Trial Master Files.
The essential requirements for the job include:
- A Master of Science in a scientific, biological, or medical science field.
- Minimum of 3 years hands-on experience in clinical study conduct.
- Strong experience using Microsoft applications (Excel, Word, PowerPoint,
Outlook). - Multilingual proficiency can be advantageous for international trials.
