
501 - 1000 employees
Founded 2000
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠Logistics
Emerald Clinical is a leading global clinical research organization (CRO) founded in the AsiaâPacific region that provides endâtoâend clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and postâmarketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.
đĽ 13 hours ago
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501 - 1000 employees
Founded 2000
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠Logistics
Emerald Clinical is a leading global clinical research organization (CRO) founded in the AsiaâPacific region that provides endâtoâend clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and postâmarketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.
⢠Support Emerald Clinical projects through statistical programming as directed by senior management or an Emerald Clinical Statistician ⢠Take the lead programmer role and mentor junior statistical programmers ⢠Perform, plan, coordinate, and implement programming for complex studies ⢠Review statistical analysis plans and mock shells ⢠Program, test, and document statistical programs for tables, figures, and listings ⢠Program and write specifications for SDTM datasets ⢠Program and write specifications for analysis datasets, including efficacy datasets and transfer files ⢠Create metadata representations of regulatory-specific and analysis datasets ⢠Conduct peer review of outputs from junior statistical programmers ⢠Program quality control checks for source data and report data issues periodically ⢠Generate randomisation lists ⢠Recruit suitably qualified and experienced clinical operations staff and allocate them to project teams ⢠Provide advanced technical expertise and independently bring project solutions to statistical programming teams for complex studies ⢠Fulfil technical team lead responsibilities for single complex studies or groups of studies ⢠Communicate with data management, project management, client statisticians, and client team members regarding requirements and timelines ⢠Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate or renegotiate deliverable timelines ⢠Participate in RFPs and bid defense meetings ⢠Use and promote established standards, SOPs, and best practices ⢠Complete mandatory training and attend required training sessions ⢠Identify resources and training supporting learning and development ⢠Comply with applicable regulations, guidelines, SOPs, project requirements, and designated systems ⢠Perform quality control and report or escalate risks and issues ⢠Participate in Emerald and internal meetings and activities ⢠Contribute to systems, tools, and processes for continuous improvement ⢠Share knowledge to facilitate organisational learning and development ⢠Comply with WH&S legislation and organisational procedures ⢠Promote and contribute to a safe, secure environment
⢠Minimum Bachelor of Science (BSc) degree in sciences related field ⢠Minimum 6 years' experience with statistical programming in SAS ⢠Minimum 6 years' experience in the CRO environment ⢠Technological proficiency in SAS ⢠Technological proficiency including Microsoft Office packages ⢠Ability and motivation to learn and develop, including sharing knowledge with others ⢠Good teamwork and willingness to help other team members ⢠Ability to see the big picture while focusing on detail and quality of work ⢠Ability to be flexible and adaptable amid changing organisational priorities and ambiguous environments ⢠Ability and willingness to travel domestically and globally
⢠Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience ⢠Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role ⢠Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role ⢠Employee Wellbeing: Programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events ⢠Global Opportunities: Exposure to diverse projects and clients through the company's international reach ⢠Purpose-driven work contributing to clinical trials that improve lives ⢠Collaboration and innovation culture ⢠Equal-opportunity employer
Apply NowđĽ 13 hours ago
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