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Senior Statistical Programmer

3 months ago

Bengaluru, India George Clinical Full time
We are expanding We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.

Who are we?

- A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence- 20 plus years of experience, ~500 people managing 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe- Full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration, and post-marketing trial- We combine scientific leadership and global operational excellence, with strong experience in renal medicine, oncology, cardiovascular and chronic diseases across various phases to improve the health of millions worldwide.

Why work with us?

- We are a global team making a difference in the world – our clinical trials improve the health of millions worldwide- Competitive salary and benefits- Flexible and agile working arrangements - onsite, hybrid, or WFH (dependent on location)- Strong and diverse Learning & Development opportunities including exposure to all aspects of clinical trials with an unparalleled network of Scientific Leaders to learn from- A focus on employee wellbeing including global employee engagement surveys, steps challenges, reward and recognition programs, team building activities, and other fun events

About the role:

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

Key Accountabilities:

- Perform, plan coordinate, and implement the following for complex studies:

1.Review statistical analysis plans and mock-shells.

2.The programming, testing, and documentation of statistical programmes for use in creating statistical tables, figures and listings.

3.The programming and specifications writing of SDTM datasets.

4.The programming and specifications writing of analysis datasets (derived datasets including efficacy datasets) and transfer files for internal and external clients.

5.Create meta-data representations of regulatory-specific and analysis data sets.

6.Conduct peer-review of outputs from junior statistical programmers.

7.The programming quality control checks for the source data and report the data issues periodically.

8.Randomisation list generation.

- 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.- 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 George Clinical and/or project requirements.

What are our expectations of candidates?

- Minimum Bachelor's degree in science-related field.- Minimum 6 years experience with statistical programming in SAS.- Minimum 6 years experience in the CRO environment.- Technological proficiency in SAS- Strong leadership and communication skills to guide and motivate a project team.- Excellent interpersonal skills to collaborate effectively with cross-functional teams.- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).- Ability to see the big picture, yet still focus on detail and quality of work.- Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.

We are searching for individuals who are excited by the idea of regional and global projects and teams, don’t want to get lost in a large CRO and are ready to have their ideas heard

You will be willing to extend yourself and take on new challenges while living our values of Mutuality, Integrity, Can-do approach, Empowerment and Excellence.

How do I apply and what if I'm interested in a role in future or want to refer someone?

Apply via LinkedIn or send your CV, referral or confidential query to and our friendly HR team across the world will reach out as appropriate soon. Please provide your full contact details, the location you are applying for, whether you are interested in a current or future opportunity and we'll be in touch. We are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.

How do I learn more about the roles and George Clinical?

Follow us on Linkedin to see our regular updates and how we celebrate our people and success across our business and projects You can also visit us at are reviewing applications as we receive them but please note that only short-listed applicants will be contacted.

Thank you for your interest in working with George Clinical. As a global business, we are committed to handling Personal Information in accordance with applicable privacy and data protection laws in the many countries in which we do business. Please see our Privacy Policy for further information.