Director Clinical Research

Job Summary:

The Director of Clinical Research will serve as the key point of contact for the global clinical R&D (CRD) team providing leadership and strategic direction for clinical trials across the AsiaPacific region. This role is responsible for planning executing and managing clinical research initiatives within CRD in alignment with global R&D priorities. The ideal candidate will have a hybrid clinical and regulatory skill set extensive experience in clinical trial operations and deep expertise in the ophthalmic industry. This role is ideal for a seasoned clinical research professional with a strategic mindset strong clinical/regulatory expertise and the ability to drive impactful clinical programs in ophthalmology.

Key Responsibilities:

Research Collaborations & Key Opinion Leader Engagement
Establish and manage cooperative research agreements with key opinion leaders (KOLs) to drive scientific advancements novel clinical endpoint development and accelerate global R&D initiatives.
Foster strong relationships with KOLs investigators and healthcare professionals to enhance clinical development strategies.
Leverage scientific expertise to engage customers and stakeholders effectively.

Clinical Trial Leadership & Regional Support
Act as the primary liaison between the global CRD team and AsiaPacific regional clinical trials ensuring seamless collaboration.
Provide local support in the planning and operational aspects of Alcon initiated clinical studies.
Oversee site selection patient recruitment data collection and compliance with global and local regulatory requirements.

Regulatory Compliance & Submissions
Maintain thorough knowledge of local regulations in the AsiaPacific region ensuring compliance with all clinical research activities.
Lead the preparation submission and presentation of clinical data to local notified bodies and health authorities as assigned.
Serve as a subject matter expert on the clinical regulatory landscape guiding crossfunctional teams on regulatory best practices.

Clinical Study & Reporting
Plan conduct and manage clinical studies from protocol development to final reporting.
Oversee clinical trial documentation including study protocols investigator brochures informed consent documents and clinical study reports.
Ensure adherence to Good Clinical Practice (GCP) guidelines ethical standards and company policies.

Product & Franchise Expertise
Possess indepth knowledge of ophthalmic products. Broad knowledge across multiple franchises including surgical contact lenses and vision care is a plus.
Provide scientific and clinical insights to support product development commercialization and postmarket surveillance.
Work closely with marketing medical affairs and commercial teams to align clinical strategies with business objectives.

Key Qualifications & Experience:
Advanced degree in Medicine Optometry Life Sciences Pharmacy or a related field (MD PhD MSc or equivalent preferred).
12 years of experience in clinical research within the ophthalmic or medical device industry.
Proven expertise in clinical trial design and regulatory submissions in the AsiaPacific region.
Strong understanding of regional regulatory requirements including interactions with health authorities and notified bodies.
Experience working with global teams and crossfunctional stakeholders.
Excellent scientific communication leadership and problemsolving skills.

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