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Jobs at Veramed (Now Hiring) — 12 open

Veramed

Senior Programmer I/II/ Principal Programmer

Bengaluru, Karnataka, India · Remote OK

Senior

Projects Portfolio Principal Programmer Purpose The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic area…

Skills: SAS, R, CDISC, Clinical Trial Programming, TFL Shells

Veramed

Principal RWE Programmer

India · Remote OK

Senior+

Principal Programmer (RWE) Purpose The role of the Principal Programmer is to provide leadership and expertise in RWE Statistical Programming to Veramed’s clients across a range of projects, clients and therapeutic areas…

Skills: R Programming, SQL, SAS, Real World Evidence, Statistical Programming

Veramed

Programmer II/ Senior Programmer I & II /Principal Programmer, Strategic Hires

Bengaluru, Karnataka, India · On-site

Senior

Principal Programmer Purpose The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Pr…

Skills: SAS, R, CDISC, Clinical Trial Programming, TFL Shells

Veramed

Senior/Principal Statistician (Oncology)

United Kingdom · On-site

Senior+

Our organisation prides itself on two key areas: delivering the highest quality statistical consultancy to clients, and providing an industry‑leading working environment that supports learning, development, and long‑term…

Skills: Statistical Leadership, Oncology Clinical Trials, Regulatory Submissions, Study Design, Sample Size Calculations

Veramed

Senior/Principal Statistician

Spain · Remote OK

Senior

Veramed prides itself on two key areas: providing the highest quality statistical and programming consultancy to our clients, and offering our employees an industry‑leading working environment with outstanding support, t…

Skills: Statistical Analysis, Clinical Research, Regulatory Submissions, Study Design, Sample Size Calculation

Veramed

Quality Assurance (QA) Manager

India · Hybrid

Senior

We have an exciting opportunity for a Quality Assurance Manager to join Veramed on a permanent basis in the UK. This role offers flexible home and/or office working, best‑in‑class training, and a competitive total reward…

Skills: Quality Management System, Internal Auditing, Vendor Audits, Regulatory Compliance, CAPA Management

Veramed

Senior Statistician

United Kingdom · On-site

Senior

The Role You will provide high-quality statistical support to one of our key-FSP clients. At Senior level you may also take on a supervisory role (e.g. line management and/or project management), depending on your experi…

Skills: Real-World Evidence, Statistical Analysis Plan, TLFs, SAS, R

Veramed

Senior/ Principal Programmer (SAS & R)

India · On-site

Senior

Principal Programmer Purpose The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Pr…

Skills: SAS, R, CDISC, Clinical Trial Programming, TFL Shells

Veramed

Principal Talent Acquisition Consultant

India · Hybrid

Senior+

Job Description: Principal Talent Acquisition Consultant Purpose The role of the Principal Talent Acquisition Consultant is to facilitate the effective staffing of Veramed and its clients by assessing the staffing needs,…

Skills: Talent Acquisition, Headhunting, Candidate Sourcing, Stakeholder Management, Team Leadership

Veramed

Principal Statistician/Manager Statistics for Consultancy Team

United States · On-site

Senior+

An opportunity has arisen for a Statistician to join Veramed’s Statistical Consultancy Business Unit full time. The opportunity will be to provide statistical support to a variety of clients. The Statistical Consultancy …

Skills: Study Design, Sample Size Calculations, Adaptive Designs, Regulatory Submissions, Statistical Analysis Plans

Veramed

Principal Statistician (RWE)

India · On-site

Senior+

Purpose The role of the Principal Statistician is to provide leadership and expertise in the statistical components of real-world evidence (RWE) to Veramed’s clients across a range of projects, clients and therapeutic ar…

Skills: R Programming, SAS Programming, SQL Programming, Real-World Evidence, Statistical Analysis Plans

Veramed

Principal Programmer (Data Anonymization)

United Kingdom · Remote OK

Senior

The purpose of the role is to support the management and delivery of clinical data anonymization and data‑sharing activities across a range of studies, clients and therapeutic areas. The individual will lead or contribut…

Skills: Data Anonymization, Project Management, Clinical Research, Risk Assessment, Quality Control

Senior Programmer I/II/ Principal Programmer

Veramed

Bengaluru, Karnataka, India • Remote OK

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Senior

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  • Full-time
  • bachelor degree, postgraduate degree
  • Posted 3d ago
  • ~40 hrs/week
  • Remote in Bangalore, Karnātaka, India

Responsibilities

Provide programming support for statistics and programming departments across various clinical trial projects and therapeutic areas. Responsibilities include authoring SAS programs, managing project delivery, and providing technical leadership or line management to staff.

Requirements

Requires a degree in a numerical discipline and between 4 to 8+ years of relevant industry experience depending on the specific level. Proficiency in SAS or R and a strong understanding of clinical drug development and ICH guidelines are essential.

Full job description

 

Projects Portfolio
 
Principal Programmer
 
Purpose
 
The role of the Principal Programmer is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).
 
Key Responsibilities
 
The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.
 
Technical:
• Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author, review and approve study TFL shells and dataset specifications
• Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice
• Identify data issues and outliers
• Complete, review and approve CDISC Validation tool reports
• Identify data and standards issues and resolve or escalate as appropriate
• Awareness of emerging standards and associated impact to ongoing and future planned trials
• Maintain proficiency in SAS and awareness of developments
• Maintain study master file documents and any other documents that are required to be audit ready
 
People Management:
• Line management of statisticians, programmers and other technical staff. Accountable for overall performance of direct reports
• Provide coaching and mentoring of staff to achieve “excellence”. Direct employee career development and ensure line reports receive appropriate training to perform their day-to-day jobs
• Interview and effectively on-board and integrate new staff members
• Provide programming technical leadership and coaching
 
Project Management:
• Oversight of key client projects/portfolios. To include:
o Being Veramed Project Manager on client accounts and projects
o Maintain the project plan
o Proactive management of resource, scope change and risks
o Manage the delivery of projects to budget
o Manage client expectations and issue resolution
 
General:
• Lead internal and client study, project and cross functional team meetings effectively
• Present study updates internally and at client meetings
• Share scientific, technical and practical knowledge within the team and with colleagues
• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
• Build effective collaborative working relationships with internal and client team members
• Ensure learnings are shared across projects or studies
• Develop and provide internal technical training where appropriate
• Lead process improvement initiatives
 
Minimum Qualification Requirements
• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)
• At least 8 years of relevant industry experience
 
Other Information/Additional Requirements
• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
• Awareness of industry and project standards & ICH guidelines
• Excellent verbal and written communication skills
• Interpersonal/teamwork skills for effective interactions
• Proficiency in data handling using SAS or other statistical software (e.g. R)
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables
• Demonstrated problem solving ability and attention to detail
• Ability to work independently and as part of a team
• Ability to manage a portfolio of projects and/or people
 
Senior Programmer I/II
 
Purpose
The role of the Senior Programmer II is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas.
 
Key Responsibilities
The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.
 
Technical:
• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review simple and complex study TFL shells
• Author and review simple and complex dataset standards
• Perform data checks and data exploration (e.g. using frequencies, histograms)
• Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice
• Complete and review CDISC Validation tool reports
• Ensure the appropriate standards are being applied and adhered to
• Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival)
• Review of project management related documents
• Maintain study master file documents and any other documents that are required to be audit ready
 
Project Management:
• Act as Lead Programmer and/or Veramed Project Manager for client projects and studies
• Maintain the project plan
• Proactive management of resource, scope change and risks
• Manage the delivery of projects to budget
• Manage client expectations and issue resolution
 
General:
• Lead internal and client study team meetings effectively
• Present study updates internally and at client meetings
• Share scientific, technical and practical knowledge within the team and with colleagues
• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
• Build effective collaborative working relationships with internal and client team members
• Seek opportunities to develop innovative ideas, sharing when appropriate
• Line management or mentorship of more junior team members
• Contribution to development of internal training materials
• Contribution to internal process improvement initiatives
 
Minimum Qualification Requirements
• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)
• At least 4 years of relevant industry experience
 
Other Information/Additional Requirements
• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
• Awareness of industry and project standards & ICH guidelines
• Excellent verbal and written communication skills
• Interpersonal/teamwork skills for effective interactions
• Proficiency in data handling using SAS or other statistical software (e.g. R)
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables
• Demonstrated problem solving ability and attention to detail
• Ability to work independently and as part of a team

 

Veramed is a B Corp accredited company which means that we use the power of business to build a more inclusive and sustainable economy meeting the highest verified standards of social and environmental performance, transparency, and accountability.

As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.

Related keywords

SASRCDISCTFLSAPCRFCSRICH GuidelinesClinical TrialsDrug DevelopmentStatistical SoftwareProject ManagementLine ManagementData ValidationB CorpNumerical Discipline

About Veramed

LinkedInVisit site

Setting the new standard for biometrics to advance the clinical trial process.

Industry
Research Services
Company size
501-1,000 employees
Founded
2012
Headquarters
London

Veramed is a Clinical Research Organization (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials. Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery. Veramed’s growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it’s long-term partnerships or rapid-fire project work, Veramed works as an extension of clients’ teams, driving efficient, dependable outcomes. A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified ®, committed to integrity and impact in everything we do. Our vision We exist to set the new standard for biometrics. By making the right decisions – for our employees, for sponsors, and for patients – we’re redefining what biometrics can deliver in clinical trials.

Offices: 5th Floor Regal House, 70 London Road, London, TW1 3QS, GB · BioHub, Alderley Park, Alderley Edge, Cheshire SK10 4TG, GB · Ty Davies, Phoenix Way, Enterprise Park, Swansea, Phoenix Way, Enterprise Park, Swansea, Wales SA7 9LA, GB · 245 First Street, Suite 1800, Cambridge, MA 02142, USA, 245 First Street, Suite 1800,, Boston, Masachuesettes MA 02142, US · Profesora Otamanovskogo Street 63, Kharkiv, Kharkiv Oblast, UA

Statistical Report WritingSAP'sCDISC Conversion (mapping + back-mapping to SDTM)Data Management ProgrammingAd-hoc Programming ServicesStatistical ConsultancyStudy DesignPROStatisticsSAS Programming
View all jobs at Veramed

About Veramed

LinkedInVisit site

Setting the new standard for biometrics to advance the clinical trial process.

Industry
Research Services
Company size
501-1,000 employees
Founded
2012
Headquarters
London

Veramed is a Clinical Research Organization (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials. Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery. Veramed’s growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it’s long-term partnerships or rapid-fire project work, Veramed works as an extension of clients’ teams, driving efficient, dependable outcomes. A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified ®, committed to integrity and impact in everything we do. Our vision We exist to set the new standard for biometrics. By making the right decisions – for our employees, for sponsors, and for patients – we’re redefining what biometrics can deliver in clinical trials.

Offices: 5th Floor Regal House, 70 London Road, London, TW1 3QS, GB · BioHub, Alderley Park, Alderley Edge, Cheshire SK10 4TG, GB · Ty Davies, Phoenix Way, Enterprise Park, Swansea, Phoenix Way, Enterprise Park, Swansea, Wales SA7 9LA, GB · 245 First Street, Suite 1800, Cambridge, MA 02142, USA, 245 First Street, Suite 1800,, Boston, Masachuesettes MA 02142, US · Profesora Otamanovskogo Street 63, Kharkiv, Kharkiv Oblast, UA

Statistical Report WritingSAP'sCDISC Conversion (mapping + back-mapping to SDTM)Data Management ProgrammingAd-hoc Programming ServicesStatistical ConsultancyStudy DesignPROStatisticsSAS Programming
View all jobs at Veramed

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