Job Purpose:
To manage clinical projects for aesthetic medical devices effectively, ensuring smooth execution of clinical affairs under a contract-based engagement, with flexibility and delivery-oriented mindset.
Responsibilities:
Acts as the primary liaison between the company and sponsors/vendors for assigned medical device studies.
Leads cross-functional teams and external partners (e.g., CROs, testing labs, device suppliers) in a contractor capacity.
Manages project deliverables tied to milestone-based payments and quality assurance.
Controls project scope and costs on a time-bound basis to mitigate financial risks under contract terms.
Ensures compliance with company SOPs, policies, and applicable medical device regulations (e.g., MDR, FDA, NMPA).Supports or leads bid defense processes for new aesthetic device projects.
Provides necessary training to project team members and supports effective team collaboration.
Tracks and reports project progress to stakeholders; provides feedback on team performance to line managers as needed.
Qualifications:
Bachelor’s degree or above in Medical, Pharmacology, Biology, Biomedical Engineering, or related fields. Diploma candidates with strong PM experience in medical devices will also be considered.
Good knowledge of medical device development processes, including regulatory pathways, GCP, and clinical trial operations for aesthetic or cosmetic indication devices.
Current GCP certificate required. Business skills such as budgeting and vendor management are a plus.
Minimum 6–8 years of industry experience, including at least 4 years of project management experience in medical devices. Experience in aesthetic devices (e.g., laser, RF, ultrasound, body contouring) is highly preferred.
Fluent in written and spoken English; local language fluency required.
Excellent command of Microsoft Office and familiarity with CTMS, eTMF, or device trial tracking tools.
Strong project management and time management skills; ability to work independently as a contractor.
