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Novotech Hiring for Clinical Data Programmer And Manager

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Novotech

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Computer Science, Data Science, Mathematics, Clinical Sciences

Bangalore

2 - 10 Years

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Novotech, a global full-service Contract Research Organization (CRO), is hiring for two clinical data management and programming roles. The available opportunities include Clinical Data Programmer II and Clinical Data Manager.

These Novotech jobs are suitable for professionals with backgrounds in clinical research, clinical data management, life sciences, computer science, data science, mathematics, business intelligence, and statistical programming.

Candidates with experience in SAS, Python, R, SQL, EDC systems, Power BI, Spotfire, Tableau, clinical data visualization, data cleaning, and clinical trial data management may find these opportunities particularly relevant.


Job Details

DetailsInformation
CompanyNovotech
IndustryClinical Research / CRO / Biotechnology
Job RolesClinical Data Programmer II, Clinical Data Manager
Employment TypeFull-time
LocationIndia*
Posted DateSeptember 14, 2026

1. Clinical Data Programmer II

Job Overview

The Clinical Data Programmer II is responsible for analyzing clinical and operational data and developing reports, dashboards, visualizations, tables, and listings to support clinical studies.

The role works closely with Clinical Data Managers (CDMs), Clinical Data Reviewers (CDRs), Project Managers (PMs), and other clinical study stakeholders.

This position is ideal for professionals with expertise in clinical data programming, business intelligence, statistical programming, clinical data visualization, SAS, Python, R, SQL, and EDC systems.

Key Responsibilities

The Clinical Data Programmer II will:

  • Gather reporting and visualization requirements from clinical study stakeholders.
  • Develop clinical data visualizations, graphs, dashboards, tables, and listings.
  • Support clinical data inspection and quality control activities.
  • Assist with clinical data reconciliation and clinical or medical review.
  • Analyze operational performance of clinical sites.
  • Support risk-based quality management approaches.
  • Work with Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs).
  • Extract clinical data from EDC systems and other data sources.
  • Integrate and transform clinical and external datasets.
  • Develop and validate programs through DEV, UAT, and PROD environments.
  • Create reports and dashboards using Business Intelligence tools.
  • Conduct data visualization review sessions with study teams.
  • Update reports and dashboards based on stakeholder change requests.
  • Train users on data visualization platforms.
  • Maintain project documentation and timesheets.
  • Participate in Clinical Data Visualization and Biometrics team activities.
  • Ensure compliance with corporate SOPs and regulatory guidelines.
  • Support process improvement and reusable programming templates.

Required Skills

Candidates should have knowledge or experience in:

  • Clinical Data Programming
  • SAS Programming
  • Python
  • R Programming
  • SQL
  • Clinical Data Visualization
  • Business Intelligence
  • Power BI
  • TIBCO Spotfire
  • Tableau
  • Qlik
  • Electronic Data Capture (EDC) Systems
  • Clinical Data Review
  • Data Extraction
  • Data Integration
  • Data Transformation
  • Data Reporting
  • Dashboard Development
  • RBQM
  • Centralized Monitoring
  • Medidata Clinical Data Studio (CDS)
  • CluePoints
  • JReview
  • Power Automate
  • Clinical Study Data Structures

Qualification and Experience

Candidates should have:

  • A Graduate degree in Computer Science, Data Science, Mathematics, Life Sciences, or a related field.
  • At least two years of relevant experience.
  • Experience in Business Intelligence, Data Science, Data Analysis, Clinical Data Management, or Clinical Data Programming.

Relevant experience in a:

  • Pharmaceutical company
  • Contract Research Organization (CRO)
  • EDC software provider

may be beneficial.


2. Clinical Data Manager

Job Overview

The Clinical Data Manager (CDM) is responsible for planning, managing, and controlling clinical data management activities throughout a clinical trial.

The role ensures that clinical trial data management activities comply with:

  • Client requirements
  • Study protocols
  • Data Management Plans
  • Good Clinical Data Management Practices (GCDMP)
  • Regulatory requirements
  • Standard Operating Procedures (SOPs)

The Clinical Data Manager works as part of the project team and collaborates with Project Managers, clients, clinical teams, monitoring teams, and external service providers.


Key Responsibilities

The Clinical Data Manager will:

  • Plan and manage clinical data management activities.
  • Assess project feasibility from a data management perspective.
  • Understand project agreements and scope requirements.
  • Collaborate with Project Managers on project planning and risk mitigation.
  • Participate in project team meetings.
  • Support preparation of Requests for Proposals (RFPs).
  • Develop and maintain Data Management Plans.
  • Design and review clinical database structures.
  • Review validation rules and consistency checks.
  • Support Clinical Data Management software operations.
  • Manage clinical trial data entry processes.
  • Perform data cleaning and data validation activities.
  • Develop key Data Management documents.
  • Coordinate with clients and clinical study stakeholders.
  • Work with external service providers.
  • Support protocol development when required.
  • Train and support junior Data Management staff.
  • Participate in process improvement initiatives.
  • Manage study financial projections.
  • Maintain monthly project financial information.
  • Identify and manage changes in project scope.
  • Support cross-functional clinical research and regulatory projects.
  • Participate in internal technology and business development initiatives.

Qualification and Experience

Candidates applying for the Clinical Data Manager job at Novotech should have:

  • A Graduate degree in Clinical Sciences, Life Sciences, or a related field.
  • Approximately 6 to 10 years of relevant experience in clinical research, pharmaceutical, or related industries.

Relevant candidates may have backgrounds in:

  • Clinical Data Management
  • Clinical Research
  • Clinical Operations
  • Pharmaceutical Sciences
  • Life Sciences
  • Clinical Trial Management

Who Can Apply?

Clinical Data Programmer II

The following educational backgrounds may be suitable:

  • B.Sc / M.Sc Life Sciences
  • B.Pharm
  • M.Pharm
  • Pharm.D
  • B.Tech / M.Tech
  • B.Sc / M.Sc Computer Science
  • Data Science
  • Mathematics
  • Statistics
  • Biotechnology
  • Bioinformatics
  • Other related fields

Relevant technical and clinical data experience is important.


Clinical Data Manager

Suitable educational backgrounds include:

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • B.Sc Life Sciences
  • M.Sc Life Sciences
  • Biotechnology
  • Clinical Research
  • Other Clinical or Life Science-related degrees

Candidates should have substantial relevant experience in Clinical Data Management or clinical research.


Key Skills for These Novotech Jobs

Clinical Data Programmer II

  • SAS
  • Python or R
  • SQL
  • Power BI
  • Spotfire
  • Tableau
  • Clinical Data Visualization
  • EDC Systems
  • Data Integration
  • Data Transformation
  • Dashboard Development
  • RBQM

Clinical Data Manager

  • Clinical Data Management
  • GCDMP
  • Clinical Trial Data
  • Data Cleaning
  • Data Validation
  • Database Design
  • Edit Checks
  • Data Management Plans
  • Project Management
  • Stakeholder Management
  • SOP Compliance
  • Regulatory Compliance

Why Join Novotech?

Novotech is a global CRO operating across multiple regions and supporting clinical research and biotechnology development.

According to the provided job information, Novotech offers employee-focused programs and benefits that may include:

  • Flexible working options
  • Flexible leave entitlements
  • Paid parental leave
  • Wellness programs
  • Professional development programs
  • Mentorship opportunities
  • Career development support
  • Inclusive workplace initiatives
  • Collaborative global teams
  • Flexible benefits through the NovoLife framework

Benefits may vary depending on location, role, and employment terms.


Salary Expectations

The official salary was not specified in the provided job descriptions.

Based on the responsibilities and typical market ranges, the following are estimated salary ranges only:

Clinical Data Programmer II

Estimated Salary: โ‚น6 LPA โ€“ โ‚น12 LPA

Clinical Data Manager

Estimated Salary: โ‚น10 LPA โ€“ โ‚น22 LPA

Actual compensation may vary based on:

  • Candidate experience
  • Technical skills
  • Location
  • Interview performance
  • Internal compensation policies
  • Total responsibilities

Candidates should confirm the final salary package during the recruitment process.


How to Apply

Application Link For Clinical Data Programmer II

Application Link For Clinical Data Manager

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