Director Clinical Program & Performance-APAC

Job  :
United Kingdom Posted:
Job Family:
Operations - DHSJob Function: ARS-Research Generalist/Multidiscipline

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Regular About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better data leads to better decisions in healthcare. We embrace AI and advanced technologies to enhance every aspect of what we do, from data analysis to operational efficiency.

Our teams work at the intersection of science, technology, and patient experience, delivering digital solutions powered by AI innovation that make clinical trials more efficient, more accurate, and more accessible around the world. Trusted by leading pharmaceutical companies and CROs, our platforms and services support studies across more than 90 countries and have contributed to hundreds of new drug approvals.

If you are motivated by meaningful work, global impact, and innovation in clinical research and digital health — including the opportunity to work with cutting-edge AI technologies — you will find purpose and opportunity at Signant Health. About the Role The Director, Clinical Services is a senior leadership role responsible for the overall delivery, quality, and development of a team of Clinical Scientists.

Reporting to the Senior Director, Clinical Services, this individual provides scientific and clinical expertise to support business development efforts, endpoint quality programs, and cross-functional initiatives across eCOA, data analytics, and product development. The Director plays a key role in building team capability, driving consistency in clinical methodology, and maintaining Signant Health's reputation as a scientific leader. This role is open to candidates based anywhere in the UK to support APAC Regions.

Fluency in Japanese and English is required (written and spoken); proficiency in a third language is preferred. Some international and domestic travel is expected (up to 25%). Key Accountabilities Conduct all activities in full accordance with Good Clinical Practice (GCP) guidelines. Ensure effective construction and implementation of training programs and endpoint quality methodologies. Advise Clinical Scientists on all aspects of studies including eCOA, training material design, endpoint strategy, and data analytics.

Provide ongoing career development, coaching, mentoring, and performance feedback to direct reports. Work with Clinical Science Team Managers to ensure appropriate and continuing training for clinicians across the department. Identify training needs across the organization; organize and deliver training initiatives accordingly. Provide oversight and input to clinical and product teams to ensure consistent development and implementation of clinical products and services.

Develop and manage quality assurance processes; write, review, and update SOPs and work instructions. Participate in and provide clinical science input for scopings, proposal writing, and bid defences. Maintain and develop customer relationships as well as relationships with external clinical resources. Knowledge, Skills & Attributes Essential:
Advanced degree in science or healthcare; clinical trial research experience strongly preferred. Fluency in Japanese and English required (written and spoken); proficiency in a third language (e.g., Mandarin or another Asian language) preferred. Proven ability to teach, mentor, and develop clinical staff at varying levels of seniority. Excellent scientific writing and oral communication skills; confident and credible presenter. Knowledge of statistics;

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