Senior Clinical Project Manager (FSP)

Job requirements

History of successful managerial experience on projects

• Demonstrate a proven history of successful managerial experience in clinical trials.
• Effectively lead team in the execution of clinical studies to maximize the value of clinical studies

 Results driven behavior

• Always maintain a focus on the objectives and anticipated outcomes of the clinical trial,
• ensuring that all components are effectively advanced to meet the established goals.
• Adapt work strategies and plans with flexibility in response to trial progress and feedback on outcomes. Enhance the trial process to improve both efficiency and quality.

Establish robust alliances with both internal and external stakeholders

• Establish and maintain close collaborative relationships with internal team members. Foster
• effective communication and collaboration among team members to facilitate the smooth
• progression of the trial.
• Ensure consistent communication and coordination with external stakeholders.
• Exhibit good teamwork and coordination skills in cross-departmental, global and interinstitutional collaborations.

Self-motivation and adaptability

• Demonstrate a robust sense of self-motivation, exhibiting the capacity to actively and
• enthusiastically engage in clinical trial work. Be able to swiftly adapt to and devise effective
• solutions for the complex and dynamic situations, as well as unforeseen challenges
• encountered in clinical trials, while ensuring continuity and stability in work processes.
• Demonstrate a commitment to continuous learning and skill acquisition to adapt to the ever evolving landscape of clinical trial regulations and technologies.

Academic / Professional Qualification

• Bachelor or higher degree in Science, Medical or Pharmaceutical Background

Working experience (No. of years / Job function / Business types)

Essential

• 10 years’ experience in clinical research studies/programs in a pharmaceutical company or CRO setting. - About 5 years of global project management experience.

Desirable

• Clinical research experience in multinational pharmaceutical company.
• Experience of collaborating with global team and cross functional team.

COMPETENCIES (Skill / Knowledge / Technical / Training requirements)

Skills Requirements

• Leadership Skills as the leader role of project team. Strong interpersonal skills, with the ability to work effectively with others at all levels of the organization.
• Good communication: be able to convey information clearly and accurately. Strong interpersonal skills with the ability to work ,effectively with others at all levels of the organization
• Learning agility: swiftly acquire new knowledge and skills and apply effectively in practical works.
• Presentation skills: confidently and fluently delivering project introductions, progress reports, and outcome demonstrations. Proven ability to deliver training
• Build relationship: Creates good impressions with people and proactively builds a network of key contacts (internal and external). Knows who is important and has good relationship with those people. Builds trust quickly, listen to other’s points and can talk easily to people from a wide range of backgrounds. Inspires team through impactful and compelling communications.

Knowledge

• Trial Implementation: proficient in all phases of trial processes including planning, initiation, execution, and closure; adept at efficiently coordinating trial resources while adhering to established timelines.
•  Knowledge of protocol design of writing and implementation is desired.
• Good understanding of the data management process and impact of different data management tools on the study management process.
• Full understanding of GCP. Familiar with company SOPs. Good Project Leadership and management skill. Good leadership skills. Able to establish and maintain excellent relationships and partnerships with investigator site staff and study team members. Knowledge of regulatory requirements related to study management activities.
• Regulatory Requirements: comprehensive understanding of local regulatory requirements related to drug supervision. And also know about global regulatory requirements.

Language ability

• Good written and verbal communication skills in English (MUST) and Chinese.

Computer literacy

• Microsoft Office and AI software.