The executive will play a pivotal role in shaping the company's therapeutic direction, accelerating clinical programs, and ensuring regulatory alignment across key markets.
Client Details
Our client is a global biopharmaceutical company focused on the discovery and development of novel antibody therapeutics in immunology and oncology. With a robust pipeline and cutting-edge technology platforms, the company is committed to delivering transformative medicines to patients worldwide.
Description
Key Responsibilities:
- Lead and oversee clinical development strategies for all pipeline programs.
- Develop and execute regulatory strategies to support global product approvals.
- Evaluate early-stage assets based on unmet medical needs, clinical value, and scientific differentiation.
- Provide medical leadership in cross-functional project teams and strategic decision-making.
- Foster relationships with regulatory agencies, key opinion leaders, and external partners.
- Ensure compliance with international clinical and regulatory standards.
Profile
Qualifications:
- Medical Doctor Degree specialization in immunology, oncology, or related fields preferred. PhD on the top is preferred.
- 15+ years of experience in clinical development and regulatory affairs within the pharmaceutical industry, global pharma and biotech
- Proven leadership in leading and managing clinical trials and regulatory submissions.
- Strong strategic thinking and ability to operate in a fast-paced, innovative environment.
- Excellent communication and stakeholder engagement skills.
Job Offer
- Competitive annual salary in the range of $400000 to $500000 USD.
- Permanent position in Shanghai with growth opportunities in the life sciences industry.
- Access to local perks and benefits to support work-life balance.
- Opportunity to lead impactful clinical and medical initiatives.
If you are ready to take on this exciting role as Chief Medical Officer in Shanghai, we encourage you to apply and join a leading organization in the life sciences industry
Desired Skills and Experience
Qualifications:
MD or equivalent advanced degree in medicine; specialization in immunology, oncology, or related fields preferred.
15+ years of experience in clinical development and regulatory affairs within the biopharmaceutical industry.
Proven leadership in managing global clinical trials and regulatory submissions.
Strong strategic thinking and ability to operate in a fast-paced, innovative environment.
Excellent communication and stakeholder engagement skills.
MPI does not discriminate on the basis of race, religion, sex, sexual orientation, gender identity or expression, age, disability, marital status, or based on an individual's status in any group or class otherwise protected under applicable human rights legislation. MPI encourages applications from minorities, women, the disabled and all other qualified applicants