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Mgr Cdm Programming ( Veeva, Sas, Python )

Thermo Fisher Scientific
1+ years
20-40 LPA
Bangalore, Remote, India, India
10 June 11, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager – Clinical Data Management Programming

Company: Thermo Fisher Scientific
Department: Clinical Data Management Programming
Work Schedule: Monday–Friday (Standard)
Work Environment: Office-Based
Job Type: Full-Time


Experience Level

  • Bachelor's degree in Life Sciences, Computer Science, Statistics, Biotechnology, Pharmacy, or related field

  • 5+ years of Clinical Data Management Programming experience

  • 1+ year of team leadership/people management experience

  • Manager-Level Position


Salary

Estimated market salary: ₹20–40 LPA CTC, with experienced CDM Programming Managers in global CROs potentially earning ₹40–55 LPA.


Role Summary

The Manager – Clinical Data Management Programming is responsible for leading a team of Clinical Data Programmers, managing project delivery, overseeing database programming activities, ensuring quality and compliance, and supporting business growth initiatives. The role combines technical expertise in clinical databases and programming with people leadership and project management responsibilities.


Key Responsibilities

People Leadership

  • Manage and mentor Clinical Data Programming staff.

  • Conduct hiring, onboarding, performance reviews, and career development discussions.

  • Provide coaching and technical guidance.

  • Manage resource allocation and workload distribution.

  • Approve leave, timesheets, and operational requests.


Clinical Database Programming

  • Lead design, build, and testing of clinical databases.

  • Oversee development and validation of edit checks.

  • Ensure database quality and compliance.

  • Support database enhancements and issue resolution.


Data Integration & Management

  • Lead data import and migration activities.

  • Define data structures and mapping requirements.

  • Ensure data accuracy and integrity across systems.

  • Support clinical data review processes.


Programming & Reporting

  • Develop and oversee:

    • SAS Programs

    • SQL Queries

    • Data Listings

    • Review Reports

    • Clinical Data Outputs

  • Ensure timely and accurate project deliverables.


Process Improvement & Innovation

  • Drive automation and process optimization initiatives.

  • Develop standardized reporting tools and applications.

  • Partner with IT teams on system enhancements and troubleshooting.

  • Improve operational efficiency across projects.


Project & Client Management

  • Track project timelines, budgets, and resources.

  • Serve as a key client-facing contact.

  • Manage project risks and escalations.

  • Ensure project delivery meets quality and budget expectations.


Business Development Support

  • Participate in proposal and bid development activities.

  • Provide technical input for new business opportunities.

  • Support client presentations and solution discussions.


Quality & Compliance

  • Ensure compliance with:

    • ICH-GCP

    • SOPs

    • Regulatory requirements

    • Client standards

  • Maintain inspection and audit readiness.

  • Monitor quality metrics and corrective actions.


Required Qualifications

Education

  • Bachelor's Degree or equivalent qualification in:

    • Computer Science

    • Statistics

    • Life Sciences

    • Biotechnology

    • Pharmacy

    • Related disciplines

Professional Experience

  • 5+ years in Clinical Data Management Programming.

  • Experience managing clinical databases and programming deliverables.

  • 1+ year of leadership or supervisory experience.


Key Technical Skills

  • SAS Programming

  • SQL

  • Clinical Database Design

  • Edit Check Programming

  • Data Validation

  • Clinical Data Review

  • RDBMS (Relational Database Management Systems)

  • Crystal Reports

  • JReview

  • Data Integration


Industry Knowledge

  • Clinical Trials

  • Clinical Data Management (CDM)

  • GCP (Good Clinical Practice)

  • Regulatory Compliance

  • CRO Operations

  • Database Lifecycle Management


Soft Skills

  • Team Leadership

  • Stakeholder Management

  • Client Communication

  • Strategic Thinking

  • Problem Solving

  • Decision Making

  • Presentation Skills

  • Project Management


Ideal Candidate

A Clinical Data Management Programming professional with strong database and programming expertise, leadership experience, and the ability to manage teams, projects, and client relationships in a global CRO environment. Experience with SAS, SQL, clinical databases, and process improvement initiatives is highly desirable.