Manager – Clinical Data Management Programming
Company: Thermo Fisher Scientific
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-based
Industry: Clinical Research / CRO / Pharma Services
Expected Salary
₹18–35 LPA CTC (typically ₹22–30 LPA for candidates with strong SAS/SQL + clinical data leadership experience)
Role Overview
The Manager – Clinical Data Management Programming leads clinical data programming operations, overseeing project delivery, team management, and client interactions. The role is responsible for database design, edit check programming, data processing workflows, and ensuring compliance with regulatory and quality standards across clinical trials.
Key Responsibilities
Team Leadership & People Management
Manage, mentor, and develop CDM programming staff.
Handle hiring, performance reviews, promotions, and employee development.
Approve workload distribution, leave, overtime, and resource planning.
Drive team engagement and capability building.
Clinical Data Programming Operations
Lead or oversee:
Clinical database design and build
Edit checks development and validation
Data import and transformation processes
Data listings for review and reporting
Ensure timely delivery of project milestones.
Project & Client Management
Track project timelines, budgets, and resource allocation.
Act as key liaison with clients and stakeholders.
Support bid preparation and business development activities.
Process Improvement & Tools
Develop and enhance reporting tools and automation solutions.
Collaborate with IT to resolve system issues.
Improve efficiency through process optimization and standardization.
Compliance & Quality
Ensure adherence to GCP guidelines and SOPs.
Maintain high standards of data integrity and regulatory compliance.
Required Qualifications
Education
Bachelor’s degree in Life Sciences, Computer Science, Statistics, or related field.
Experience
5+ years in clinical data programming or clinical data management.
1+ year in leadership or supervisory role.
Technical Skills
Core Tools & Systems
SAS (advanced)
SQL (advanced)
Crystal Reports
JReview
Relational Database Management Systems (RDBMS)
Veeva EDC or similar CDM systems
Domain Knowledge
Clinical trial data structures
GCP (Good Clinical Practice)
Clinical study lifecycle and regulatory requirements
Leadership & Soft Skills
Strong team management and mentoring capability
Excellent communication and stakeholder management
Strong problem-solving and analytical skills
Ability to manage multiple projects under tight deadlines
Decision-making and process improvement mindset
Preferred Qualifications
Experience in global CRO or pharmaceutical clinical trials.
Exposure to large-scale multi-country studies.
Experience in automation or advanced reporting tools.
Strong budgeting and project forecasting experience.
Experience interacting with clients in regulated environments.
Ideal Candidate Profile
Mid-senior clinical data professional with leadership experience.
Strong SAS/SQL programming background.
Proven ability to manage teams and deliver clinical trial data outputs.
Comfortable handling client-facing responsibilities.
Strong understanding of regulated clinical research environments.
Career Growth
Manager → Senior Manager → Associate Director → Director → Head of Clinical Data Programming
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