Clinical Lead
Adecco
- Sinyi, Taipei City
- Permanent
- Full-time
- Good communication with good interpersonal skills
- Advanced degree in a scientific/bioengineering field (Ph. D or M.D.)
- clinical affairs/research project/medical affairs management is preferred
- Monitor scientific literature to stay updated on scientific knowledge and market trends, contributing to the development of clinical evidence strategies.
- Identify evidence gaps and market opportunities to design and execute evidence strategies that meet local evidence needs and support reimbursement initiatives.
- Contribute to the development and implementation of clinical and medical strategies aligned with business goals, ensuring timely and budget-compliant execution of evidence generation initiatives.
- Collaborate with the commercial function to understand market trends and support business goals through Clinical Affairs activities.
- Collaborate with internal stakeholders (Regulatory Affairs, Global Access Value Economics, Global Public Affairs, Commercial functions) and external stakeholders (advisory boards, KOLs, medical/surgical societies) to develop evidence generation strategies, review evidence concepts, and develop study/evidence designs.
- Plan and execute site selection, investigator selection, patient recruitment analysis, and support the creation of study-related documents (protocols, case report forms, informed consents, clinical trial agreements).
- Participate in data analysis, interpretation, and synthesis, contributing to the development of clinical study reports and scientific publications.
- Ensure compliance with corporate and regulatory requirements, including authoring, reviewing, and revising Clinical Operations Standard Operating Procedures (SOPs) for the region/country.
- Provide an in-depth understanding of the importance of metrics and milestones.
- Manage budgets and resources effectively and efficiently.
- Routinely solve complex problems to enable significant team progress.
- Previous experience in developing scientific publication strategies
- Strong knowledge of clinical and outcomes research study design
- Experience in conducting literature searches, reviews, and data appraisal
- Excellent interpersonal skills and ability to collaborate with healthcare professionals
- Experience in protocol development and medical writing
- Knowledge of Good Clinical Practice, 21 CFR Part 11, and local regulations
- Understanding of clinical trials, study design, and basic ICH/GCP knowledge
- Ability to work effectively in cross-functional teams and matrix environments
- Ability to build relationships, influence stakeholders, and drive projects forward
- Quick learner with a self-starter attitude towards different surgical specialties
- Dedicated to meeting aggressive timelines and managing multiple projects
- Entrepreneurial mindset and willingness to take risks
- Fluency in Mandarin and En