Experienced statistical-programming professionals looking for senior leadership opportunities in clinical research can apply for the Emmes Associate Director/Director, Statistical Programming 2026 position in Bengaluru, India.
Table of Contents
Emmes Group is recruiting an experienced professional to lead statistical-programming activities supporting:
Clinical trials.
Clinical development programmes.
Regulatory submissions.
Post-marketing studies.
The position is:
Regular Full-Time
and based in:
Bengaluru, India.
The official Job ID is:
3582.
This is a senior-level leadership position, not an entry-level or graduate software-engineering opportunity.
Candidates need a:
Master’s degree
in an appropriate discipline and at least:
12 years of statistical-programming experience
within the pharmaceutical, biotechnology or Contract Research Organization industry.
Applicants also need at least:
Five years of experience in a leadership or management-level role managing programming teams.
The position requires advanced knowledge of:
SAS programming.
CDISC standards.
SDTM.
ADaM.
Regulatory submissions.
Clinical-trial programming.
Candidates with extensive statistical-programming experience who want to contribute to technology-enabled clinical research can consider this senior opportunity.
About Emmes Group
Emmes Group operates in the clinical-research sector and describes itself as a:
Technology-enabled full-service CRO.
The organization works to modernize clinical trials and accelerate the development of therapies.
Emmes says it brings together:
People, Science and Technology
to collaborate with customers and create global health impact.
The company has more than:
47 years of scientific experience.
Its research experience includes areas such as:
Cell and gene therapy.
Vaccines.
Infectious diseases.
Ophthalmology.
Rare diseases.
Neuroscience.
The organization emphasizes the combination of scientific expertise with technology to advance clinical research.
About the Statistical Programming Position
The official position is:
Associate Director/Director, Statistical Programming.
The successful candidate will serve as both a:
Strategic
and:
Operational
leader.
They will oversee statistical-programming activities across biopharmaceutical clinical-development programmes.
This includes responsibility for high-quality, regulatory-compliant programming deliverables supporting:
Clinical trials.
Regulatory submissions.
Post-marketing studies.
Job Location
The official location is:
Bengaluru, India.
The vacancy identifies the position as:
Regular Full-Time.
The supplied posting does not establish that this is a remote or work-from-anywhere position.
Candidates should therefore assess the opportunity based on the stated Bengaluru location.
Career Area
The vacancy is classified under:
Biometrics/Biostatistics.
Although candidates need significant technical programming expertise, this is not presented as a conventional software-engineering role.
The work focuses specifically on:
Statistical programming for clinical research and regulatory activities.
Leadership Responsibilities
A major component of the position is:
Leadership and Team Management.
The successful candidate will:
Lead and manage a team of statistical programmers.
Establish organizational structures.
Develop hiring plans.
Build career-development frameworks.
Provide mentorship.
Provide guidance.
Manage performance.
The candidate will work with professionals including:
Senior managers.
Programming leads.
Staff programmers.
Managing Statistical Programmers
The Associate Director/Director will be responsible for leading the statistical-programming team.
This requires more than technical SAS expertise.
Candidates need demonstrated experience in:
People management.
Technical leadership.
Mentoring.
Performance management.
Strategic decision-making.
Resource management.
The experience requirements reflect the senior nature of these responsibilities.
Strategic Planning
The successful candidate will define and execute a:
Global statistical-programming strategy.
This strategy must align with broader:
Clinical goals.
Regulatory goals.
Organizational objectives.
The candidate should therefore be capable of translating clinical-development requirements into an effective programming strategy.
Clinical Trial Programming
The role oversees programming support for clinical trials ranging from:
Phase I through Phase IV.
This gives the position broad exposure across the clinical-development lifecycle.
Candidates need substantial previous experience working in pharmaceutical, biotechnology or CRO statistical-programming environments.
Integrated Summaries
The successful candidate will also oversee programming associated with:
Integrated summaries
and:
Regulatory submissions.
This requires a strong understanding of how statistical-programming deliverables contribute to regulatory packages.
Corporate Planning
The Associate Director/Director will contribute to corporate-level activities involving:
Planning.
Budget forecasting.
Resource allocation.
Vendor partnerships.
This further demonstrates that the role is not simply an individual contributor programming position.
The successful candidate must understand how programming functions fit within broader organizational and clinical-development strategies.
Technical Oversight
Technical leadership is another major part of the position.
The successful candidate must ensure high-quality programming deliverables.
These include:
SDTM datasets
ADaM datasets
and:
Tables, Listings and Figures — TLFs.
Candidates therefore need deep technical knowledge of clinical statistical programming.
SDTM
Experience with:
Study Data Tabulation Model — SDTM
is particularly important.
The successful candidate must understand CDISC standards and provide oversight of programming outputs used in clinical development and regulatory submissions.
ADaM
Expertise in:
Analysis Data Model — ADaM
is also essential.
Candidates need deep familiarity with both:
SDTM
and:
ADaM.
These are specifically identified in the official qualifications.
Tables, Listings and Figures
The successful candidate will oversee production of:
Tables
Listings
and:
Figures
commonly referred to as:
TLFs.
The candidate must ensure these deliverables meet required standards of quality and regulatory compliance.
Regulatory Submission Planning
The position includes responsibility for:
Submission planning and execution.
This includes work involving:
eCTD packages
and:
Define.xml generation.
Candidates should therefore have direct experience supporting regulatory submissions rather than only general programming experience.
CDISC Expertise
The successful candidate will serve as a:
Technical expert on CDISC implementation.
The role also provides governance over:
Global standards.
Programming compliance.
Technical consistency.
Candidates need advanced understanding of how CDISC standards are implemented across clinical-development programmes.
SAS Programming
Expert knowledge of:
SAS programming
is required.
This is one of the central technical requirements of the position.
Applicants should have substantial experience using SAS within:
Pharmaceutical.
Biotechnology.
CRO.
Clinical-research.
environments.
Regulatory Submissions
Candidates need proven experience supporting:
NDA
BLA
and:
MAA
submissions.
This is an important distinction from general statistical-programming positions.
Applicants should have experience working with programming outputs that support formal regulatory processes.
NDA Experience
The official qualifications specifically identify experience supporting:
New Drug Application — NDA
submissions.
Candidates should clearly present relevant regulatory-submission experience in their professional history.
BLA Experience
Experience supporting:
Biologics License Application — BLA
submissions is also required at a high level.
This can be particularly relevant to candidates with backgrounds in biotechnology and biologics development.
MAA Experience
The vacancy also identifies:
Marketing Authorization Application — MAA
experience.
This reflects the global regulatory scope of the position.
Responding to Regulatory Queries
Candidates should also have experience:
Responding to regulatory queries.
This means the successful candidate may need to work with regulatory teams when authorities raise questions concerning submission data or programming outputs.
Cross-Functional Collaboration
The Associate Director/Director will work across multiple functions.
These include:
Biostatistics
Data Management
Clinical Operations
Regulatory Affairs
and:
External partners.
The position therefore requires strong collaboration skills alongside technical and leadership capabilities.
Senior Leadership Forums
The successful candidate will act as the:
Primary programming representative
in senior leadership forums.
This requires an individual who can communicate complex statistical-programming matters to senior stakeholders.
Regulatory Interactions
The role can also involve:
Regulatory interactions.
Candidates should therefore be comfortable representing statistical-programming functions in high-level discussions where technical accuracy and professional communication are essential.
CRO Partnerships
The successful candidate will oversee strategic relationships with:
Contract Research Organizations — CROs.
The objective is to ensure:
Delivery quality.
Strategic alignment.
Effective external collaboration.
This is why vendor-management experience is identified among the qualifications.
Technology Vendors
The role also includes oversight of partnerships with:
Technology vendors.
Candidates should understand how external technologies and platforms can support statistical-programming workflows.
Process Improvement
Emmes expects the successful candidate to champion:
Process optimization.
The candidate will identify opportunities to improve statistical-programming workflows and operational efficiency.
Automation
The role specifically emphasizes:
Automation.
Candidates should be comfortable identifying repetitive or inefficient processes that can be improved through appropriate technologies and programming approaches.
Innovation
Innovation is another major component of the role.
The successful candidate will lead evaluation and implementation of:
New tools.
New platforms.
New technologies.
This creates opportunities to modernize statistical-programming operations.
R Programming
Although SAS expertise is central, the vacancy also identifies:
R
as an example of technology relevant to programming innovation.
Candidates with experience using R in clinical or statistical environments may therefore bring additional useful capabilities.
Python
The vacancy also specifically mentions:
Python.
This reflects the increasing use of multiple programming languages within modern clinical-data and analytics environments.
Cloud-Based Analytics
Emmes also references:
Cloud-based analytics
as an example of technology that may be evaluated and implemented.
Candidates with experience modernizing programming environments through cloud technologies may therefore have relevant expertise.
Compliance
The Associate Director/Director must ensure compliance with:
Industry standards.
Company Standard Operating Procedures.
Regulatory expectations.
The position therefore requires both technical expertise and strong understanding of regulated clinical-research environments.
Master’s Degree Required
Applicants need a:
Master’s degree
in one of several relevant areas.
These include:
Computer Science
Statistics
Mathematics
Life Sciences
or:
A related field.
The master’s degree is identified as:
Required.
Experience Requirement
Candidates need at least:
12+ years of experience in statistical programming
within:
Pharmaceutical companies.
Biotechnology companies.
CRO organizations.
This makes the vacancy a highly experienced professional opportunity.
Leadership Experience
Applicants also need:
Five years in a leadership or management-level role
managing programming teams.
This requirement is separate from the overall 12+ years of statistical-programming experience.
Candidates should therefore demonstrate both:
Technical longevity.
Leadership progression.
Vendor Management Experience
The vacancy lists:
One year of experience managing vendors and CRO partnerships
as:
Preferred.
Candidates with experience overseeing outsourced programming or technology relationships should highlight this appropriately.
Regulatory Knowledge
Candidates need a strong understanding of:
ICH guidelines
21 CFR Part 11
and:
Global regulatory requirements.
This regulatory knowledge is essential because the programming function supports formal clinical-development and submission activities.
Communication Skills
Emmes requires:
Exceptional communication skills.
The successful candidate must communicate across:
Technical teams.
Senior leadership.
Clinical functions.
Regulatory functions.
External partners.
Vendors.
Strong communication is therefore central to the position.
Collaboration Skills
The vacancy also emphasizes:
Collaboration.
This aligns with Emmes’ broader emphasis on bringing:
People.
Science.
Technology.
together to advance clinical research.
Leadership Skills
Candidates need exceptional:
Leadership skills.
The successful professional will be responsible not only for delivering technical work but also for shaping:
Teams.
Processes.
Strategy.
Standards.
Technology adoption.
Organizational capabilities.
Qualifications at a Glance
Education: Master’s degree required
Relevant Fields: Computer Science, Statistics, Mathematics, Life Sciences or related discipline
Statistical Programming Experience: 12+ years required
Leadership/Management Experience: Five years required
Vendor/CRO Management: One year preferred
SAS: Expert knowledge required
CDISC: Deep familiarity required
SDTM: Required expertise
ADaM: Required expertise
Regulatory Submissions: Significant experience required
NDA: Relevant experience required
BLA: Relevant experience required
MAA: Relevant experience required
ICH Guidelines: Strong understanding required
21 CFR Part 11: Strong understanding required
Communication: Exceptional skills required
Leadership: Exceptional skills required
Is This a Graduate Opportunity?
No.
This is particularly important because some third-party headlines may incorrectly present the vacancy as a:
Graduate opportunity.
The official Emmes posting requires:
12+ years of statistical-programming experience
and:
Five years of leadership or management experience.
It is therefore clearly a:
Senior professional position.
Recent graduates should not interpret this vacancy as an entry-level opportunity.
Is This an Associate Software Engineer Job?
No.
The official vacancy supplied for this opportunity is titled:
Associate Director/Director, Statistical Programming.
It is not:
Associate Software Engineer.
Although the role involves programming and mentions technologies such as:
SAS.
R.
Python.
it is a senior statistical-programming leadership position within clinical research.
Publishers should therefore avoid labeling it a software-engineering graduate vacancy.
Is This a Full-Time Position?
Yes.
The official vacancy classifies the position as:
Regular Full-Time.
Is the Position Remote?
The official vacancy lists:
Bengaluru, India
as the location.
The supplied posting does not establish a remote or work-from-anywhere arrangement.
Candidates should therefore not describe it as a remote position unless Emmes separately confirms such an arrangement.
Is Visa Sponsorship Available?
The supplied vacancy does not state that Emmes will provide:
Visa sponsorship.
International applicants requiring Indian work authorization should therefore verify eligibility directly through the official recruitment process.
Is Relocation Support Available?
The supplied vacancy does not establish that:
Relocation assistance
is provided.
Candidates should therefore not advertise relocation funding as part of the employment package unless Emmes separately confirms it.
Salary
The supplied official vacancy does not provide a specific:
Salary.
Salary range.
Compensation figure.
Candidates should therefore avoid relying on unofficial salary estimates as though they were confirmed by Emmes.
Application Deadline
The vacancy text supplied does not specify a closing date.
Applicants should therefore not invent a deadline.
Candidates interested in the position should check the official recruitment portal and apply while:
Job ID 3582
remains available.
How to Apply
Candidates should apply through the:
Official Emmes recruitment system.
The relevant vacancy is:
Associate Director/Director, Statistical Programming
with:
Job ID 3582.
Applicants should carefully review the current vacancy before submitting their information because requirements and availability can change.
Important Details at a Glance
Organization: Emmes Group
Position: Associate Director/Director, Statistical Programming
Job ID: 3582
Location: Bengaluru, India
Career Area: Biometrics/Biostatistics
Employment Type: Regular Full-Time
Career Level: Senior leadership
Graduate Opportunity: No
Associate Software Engineer: No
Minimum Degree: Master’s degree
Relevant Degrees: Computer Science, Statistics, Mathematics, Life Sciences or related field
Minimum Statistical Programming Experience: 12+ years
Leadership/Management Experience: Five years
Vendor/CRO Management: One year preferred
SAS: Expert knowledge
CDISC: Deep familiarity
SDTM: Required expertise
ADaM: Required expertise
NDA/BLA/MAA Experience: Required at high level
ICH Guidelines: Strong understanding
21 CFR Part 11: Strong understanding
R/Python: Relevant to technology innovation
Remote: Not established
Visa Sponsorship: Not stated
Relocation: Not stated
Salary: Not stated
Deadline: Not stated in supplied vacancy
Application: Through official Emmes recruitment system
Who Should Consider Applying?
The position may be particularly relevant to highly experienced professionals working as:
Statistical Programming Directors.
Associate Directors of Statistical Programming.
Senior Statistical Programming Managers.
Clinical SAS Programming Leaders.
Biometrics Leaders.
Clinical Data Programming Leaders.
Regulatory Statistical Programming Professionals.
CDISC Experts.
Candidates should already have extensive experience in the pharmaceutical, biotechnology or CRO environment.
Who Should Not Treat This as an Entry-Level Opportunity?
This vacancy is not appropriate to advertise primarily to:
New graduates.
Students.
Entry-level software engineers.
Junior developers.
Candidates with no clinical-programming experience.
The experience requirements make the intended career level very clear.
Applicants need more than a decade of statistical-programming experience plus substantial leadership experience.
Why This Emmes Opportunity Stands Out
The role combines:
Technical leadership.
Clinical research.
Statistical programming.
Regulatory submissions.
People management.
Strategic planning.
Technology innovation.
The successful candidate will have the opportunity to influence programming activities supporting clinical trials from:
Phase I through Phase IV.
They will also contribute to regulatory submissions and work with technologies extending beyond traditional SAS programming, including:
R.
Python.
Cloud-based analytics.
The position therefore combines established clinical-programming expertise with the modernization of statistical-programming workflows.
Final Considerations
The Emmes Associate Director/Director, Statistical Programming 2026 opportunity is a senior full-time position based in:
Bengaluru, India.
The successful candidate will oversee statistical-programming activities supporting:
Clinical trials.
Regulatory submissions.
Post-marketing studies.
They will lead statistical programmers, establish organizational structures, support hiring and career development, define global programming strategy and ensure high-quality regulatory-compliant deliverables.
Candidates need:
A master’s degree
and:
12+ years of statistical-programming experience
within the pharmaceutical, biotechnology or CRO industry.
They must also have:
Five years of leadership or management experience managing programming teams.
Expert SAS knowledge and deep familiarity with:
CDISC
SDTM
and:
ADaM
are required.
Candidates also need proven experience supporting:
NDA, BLA and MAA submissions
and responding to regulatory queries.
Professionals with the required experience can apply through Emmes’ official recruitment platform using:
Job ID 3582.
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