Clinical Operations Director

An international pharmaceutical company is advertising a vacancy for a Clinical Operations Director in their Chinese office. This historic organisation prides itself on over a century's experience in ophthalmology, having taken initiatives in ophthalmic research, regulatory management, production, marketing, or distribution. This is an exciting opportunity to work with one of the leading establishments in ophthalmic healthcare and provide skills and expertise in the pharmaceutical commercial field.

Job Responsibilities:

• Performing overall management for assigned projects to ensure timely delivery, data quality, and budget within control.
• Implementing and driving resource strategy for Clinical Operations to meet project deliverables, timelines, and changing workloads.
• Working and reporting to North America directly and dotting line to local R&D Head.
• Accepting accountability for department SOP development, as well as renewal.
• Supporting the organization with appropriate training programs.
• Providing management coaching to the staff.
• Accepting accountability in the country for strategy related to Clinical Operations activities, including, but not limited to, feasibility, allocations, recruitment enablers, trial execution, and local customer relationships related to Clinical Operations
• Performing management to, but not limited to, clinical study start-up from any stages, budget control, initiation, patient enrolment, protocol adherence, CRF compliance, data quality to meet specified ethical, scientific, and regulatory needs.
• Developing and maintaining KOL relationships.
• Maintaining good communications and relationships with 3rd party vendors.
• Ensuring the clinical trials conduction in compliance with ICH - GCP guidelines, local regulatory requirements, SOPs, and protocols.

Skills and Requirements:

• Minimum of 10 years of experience in clinical operations in international pharmaceutical/CRO environment.
• At minimum, a Bachelor's degree.
• Good knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Expertise in risk management and contingency planning.
• Proven ability to manage budgets and resource.
• Competent in written and oral English is must.
• Demonstrable multitasking, project management, and execution skills.
• Good interpersonal skills, including communication, presentation, persuasion, and influence.

• Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
• Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Tom Tan at +86 21 51694101 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

Proclinical Staffing is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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