Senior Statistical Programmer

Emerald Clinical; Bengaluru; Hybrid; INR 1,400,000 - 2,100,000; Full time

Benefits offered by this job

Competitive compensation

Hybrid or remote options

Career growth opportunities

Job summary

Emerald Clinical Trials in Bengaluru invites a Senior Statistical Programmer to support projects, lead programming efforts, and mentor junior staff. You will review SAPs, develop programs for tables, figures and listings, and create SDTM datasets to ensure high-quality deliverables.

The ideal candidate has 6+ years of SAS programming in a CRO setting, a BSc in a science field, and strong collaboration skills. Domestic/global travel may be required; join a global team delivering impactful trials.

Qualifications

• Bachelor of Science in a sciences related field.
• Minimum 6 years SAS programming experience.
• Minimum 6 years CRO industry experience.
• Proficiency in SAS and related statistical programming.

Responsibilities

• Plan, coordinate and implement for complex studies.
• Review statistical analysis plans and mock shells.
• Develop programs for tables, figures and listings; SDTM datasets.
• Mentor junior programmers and conduct peer-review.

Skills

SAS programming

CRO experience

Statistical programming

Microsoft Office

Education

Bachelor of Science in a sciences related field

Tools

SAS software

Job description

Job Description:

Who We Are

Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.

With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.

Global Expertise. Local Insight. Real Impact.

Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.

Our 1000+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

The Senior Statistical Programmer will support Emerald Clinical projects by performing statistical programming as directed by either senior management or a Emerald Clinical Statistician, take lead programmer role and mentor junior statistical programmers.

Responsibilities

• Perform, plan co-ordinate and implement the following for complex studies:
• Review statistical analysis plans and mock shells.
• The programming, testing, and documentation of statistical programmes for use in creating statistical tables, figures and listings
• The programming and specifications writing of SDTM datasets.
• The programming and specifications writing of analysis datasets (derived datasets including efficacy datasets) and transfer files for internal and external clients
• Create meta-data representations of regulatory-specific and analysis data sets.
• Conduct peer-review of outputs from junior statistical programmers.
• The programming quality control checks for the source data and report the data issues periodically
• Randomisation list generation
• Recruit suitably qualified and experienced clinical operations staff for Emerald in a timely mannerandallocatethem to project team.
• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.
• Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.
• Directly communicate with internal team including data management, project management, and client statisticians and client team members to ensure appropriate understanding of requirements and project timelines.
• Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.
• Participating in RFPs and bid defense meetings.
• Use and promote the use of established standards, SOP and best practice

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 elevate identified risks and issues in areas of responsibility according to Emerald and/or project requirements

Customer Focus and Teamwork

• Attend and actively participate in Emerald 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 organisation

Work Health and Safety

• Comply with Work Health & S legislation and operate in accordance with established organisational WH&S practice and procedures
• Promote and contribute to a safe, secure environment for staff and visitors

About You

• 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

Competency

• Ability and motivated to learn and develop, including sharing knowledge with others
• Good teamwork and willing to help other team members
• Technological proficiency including Microsoft Office packages
• Ability to see the big picture, yet still focus on detail and quality of work
• Ability to be flexible and adaptable in a face changing organisational priorities and ambiguous environments

Additional requirements

• Ability and willingness to travel domestically & globally

Why Join Us?

At our core, Emerald Clinical Trials 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.

What We Offer

We understand that great work happens when people feel valued and supported. That’s why we provide:

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: Participate in 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: Be part of a company with international reach, offering you exposure to diverse projects and clients.

We are an equal-opportunity employer and encourage applications from all qualified candidates.