- At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region.

- We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

- Our therapeutic expertise spans renal, cardiometabolic, and oncology-areas where we make a significant impact on improving global health.

- At the heart of our success is our ability to combine global reach with local knowledge.

- Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment.

- By prioritizing people, we deliver better engagement, more accurate data, and faster results-bringing therapies to patients in need.

Why Join Us?

- At our core, Emerald Clinical is committed to transforming clinical research by putting people first-both patients and our employees.

- By joining our team, you'll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

- Here's What Makes Us Stand Out.

- Purpose-Driven Work: You'll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.

- Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.

- Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.

About The Role:

- The Associate Director - Statistical Services is responsible for global biostatistics activities (specifically statistical programming) and also manages Biostatistical resources in India and other locations in the organization, as applicable.

- The Associate Director Statistical Services leads all biostatistics activities, including support of the Business Development group, team recruiting and building, as well as being responsible for departmental coordination and study resourcing as it relates to biostatisticians and statistical programming.

Your Responsibilities:

- Serve as a consultant for other members of the biostatistics department and staff members from other departments within the company.

- Maintain knowledge and awareness of developments in biostatistics/statistical programming and clinical trial methodology, and regulatory requirements that impact on analyses.

- Coordinate and manage internal and contracted staff in accordance with organization's policies and applicable regulations.

- Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems.

- Approve actions on human resources matters.

- Work as the lead and participate in project meetings; keep up to date on project issues.

- Coordinate and participate in process improvements and interoffice/ interdepartmental task forces; oversee collection and reporting of Biostatistics metrics, implementation of revised work practices, new guidelines, and new software tools as they become available.

- Make recommendations about resource allocation for team members so as to achieve target utilization rates and project realization rates.

- Support strategy and development of organizational data analytics, as required.

- Assist in the following: Sales meetings as required.

- Overseeing proposal preparation.

- Ensuring that all proposals bid by the department have an adequate budget, and sufficiently detailed set of budget assumptions.

- Provide training, guidance and mentorship to junior and new staff.

- Manage finance for the statistical services department.

- Assist in business development and relationship building with the client.

- Training, Quality and Compliance.

- Complete mandatory training for this role within specified timelines.

- Attend mandatory training sessions required for this role.

- Identify resources and training to support learning and development within this role.

- Comply with all applicable regulations, guidelines, SOPs and project-specific requirements.

- Comply with all designated systems relevant to this role.

- Ensure own quality control of all relevant processes and activities performed.

- Report and escalate identified risks and issues in areas of responsibility according to Emerald Clinical and/or project requirements.

- Customer Focus and Teamwork.

- Attend and actively participate in Emerald Clinical meetings and other internal meetings and activities as required.

- Provide input to systems, tools and processes to support continuous improvement.

- Share knowledge with others, to facilitate learning and development across the organization.

- Work Health and Safety.

- Comply with Work Health & Safety (WH&S) legislation and operate in accordance with established organizational WH&S practice and procedures.

- Promote and contribute to a safe, secure environment for staff and visitors.

Education And Experience:

- Minimum Bachelor's degree in Biostatistics/ Engineering or science related field.

- Minimum 14 years' experience in Biostatistics/statistical programming related work.

- Prior experience in the CRO environment is preferable.