About this role
Job title: Sr Medical Advisor/ Mgr/Sr Mgr-KunTuo
About the Role This role is for a Sr Medical Advisor/ Manager/ Sr Mgr to support IQVIA's clinical research activities in China. The position focuses on medical writing, medical review, investigator interactions, and medical training to ensure trial quality and patient safety in alignment with SOPs and client requirements. The role may require travel and collaboration across departments.
What You'll Do
- Prepare and organize educational seminars on clinical research protocols and communicate with principal investigators or field experts.
- Perform medical writing for clinical trial documents per SOPs and client requirements (protocols and clinical study reports, etc.).
- Conduct medical reviews of study documents (protocols, informed consent forms, investigator brochures, CRFs, SAPs, clinical study reports, and adverse event coding).
- Develop medical monitoring plans per SOPs and project requirements to ensure quality and safety, including SAE and protocol deviation monitoring.
- Provide medical support to the clinical operations team, including site feasibility assessments, investigator selection, and initial medical discussions with investigators.
- Provide medical training and support to project teams or investigators, including creating training materials and delivering domain knowledge training.
- Attend investigator meetings and present medical content as needed.
- Participate in project kickoff meetings, study team meetings, and client meetings as required.
- Provide medical support to the BD team for new project proposals, meeting with clients as necessary to discuss medical questions.
- Establish and maintain relationships with key medical experts; regularly visit field experts to update medical progress and sustain collaboration.
- Draft SOPs for the department as needed.
- Collaborate with other departments.
- Travel as required.
- Complete tasks efficiently as assigned by the direct manager.
What We're Looking For
- Bachelor’s degree in Clinical Medicine or related field, or Master/PhD in pharmaceutical-related fields.
- For bachelor’s degree: at least 3 years of medical advisor or hospital clinical/clinical research experience; Master’s: at least 2 years; PhD: at least 1 year; equivalent qualifications considered.
- Strong clinical trial knowledge and understanding of regulatory requirements (GCP, ICH-GCP, etc.) in China.
- Proficiency in Microsoft Word, PowerPoint, and Excel.
- Excellent verbal and written communication skills (including fluency in English).
- Strong presentation and training skills.
- Strong team spirit and collaboration ability; ability to build and maintain relationships with colleagues, managers, and clients.
Nice to Have
- Equivalent education/training/experience will be considered.
Compensation & Benefits
- Salary: Not disclosed
- Work model: Hybrid (remote/home and office) with potential travel as needed
- Additional benefits not specified in the posting