🔹 Job Title: Clinical Data Management
📍 Location: Pune, India (Hybrid)
🕓 Job Type: Full-Time
🆔 Job ID: R1463811
🏢 Organization: IQVIA
🌍 Additional Locations: Available
🔗 Apply Here: IQVIA Careers
🔹 Job Category: Clinical Data Management
🎓 Qualification: Bachelor’s Degree (B.Pharm or Equivalent – Preferred)
💼 Experience: 3–4 Years Direct Data Management Experience (Including ≥1 Year as CDM Project Lead – Preferred)
🔹 Job Overview:
Manage end-to-end delivery of Clinical Data Management (CDM) services for single or multi-service projects with minimal guidance. Ensure high-quality deliverables are completed on time, within budget, and to customer satisfaction.
Provide data management expertise, lead project planning, execution, and close-out, and oversee financial, quality, and communication activities related to Data Management.
Perform the role of Data Team Lead (DTL) and mentor team members in achieving project goals.
🔹 Key Responsibilities:
📊 Project Planning & Oversight
Gather study setup requirements through discussions with stakeholders.
Lead project planning, tracking, and progress monitoring, identifying risks and implementing corrective actions.
Ensure deliverables meet contracted timelines, scope of work (SOW), and quality standards.
Support and oversee device integration validations and new technology/database revisions with minimal guidance.
Participate in study kick-off meetings, internal reviews, and sponsor meetings.
Lead internal study meetings and represent CDM during sponsor audits.
🧹 Data Quality & Cleaning
Perform and oversee regular data cleaning activities to ensure data accuracy, completeness, and timeliness.
Collaborate with programming teams for process innovation and automation.
Ensure high-quality data deliverables aligned with sponsor expectations.
📚 Documentation & Compliance
Review, revise, and maintain Core Operating Procedures and Work Instructions.
Ensure adherence to eSOPs and training compliance.
Maintain proper documentation of study activities and quality processes.
🧑🏫 Team Leadership & Training
Lead and support training programs for new joiners in CDM processes.
Provide guidance to team members in project execution and best practices.
Foster collaborative communication with line managers and cross-functional teams.
⚙️ Continuous Improvement
Identify opportunities for process optimization and technology adoption.
Contribute to innovation initiatives within the CDM function.
Ensure compliance with GCP, ICH, and regulatory guidelines in all CDM activities.
🔹 Required Skills:
|
Skill Area |
Proficiency |
|---|---|
|
Clinical Data Management |
Advanced |
|
Drug Development Lifecycle Knowledge |
Advanced |
|
Project Planning & Oversight |
Advanced |
|
Data Cleaning & Quality Control |
Advanced |
|
Device Integration & EDC Systems |
Intermediate |
|
MS Office (Excel, Word, Outlook) |
Advanced |
|
English Communication (Written & Spoken) |
Advanced |
|
Process Documentation & SOP Compliance |
Advanced |
|
Cross-Functional Collaboration |
Intermediate |
🔹 Educational Requirements:
Bachelor’s Degree (B.Pharm or Equivalent) – Preferred
🔹 Experience Requirements:
3–4 years in Clinical Data Management
≥1 year as CDM Project Lead (Preferred)
🔹 About IQVIA:
IQVIA is a global leader in clinical research, data analytics, and healthcare intelligence, offering technology-driven insights and services to life sciences organizations. We create intelligent connections to accelerate drug development, commercialization, and patient outcomes.
🌐 Learn more: https://jobs.iqvia.com
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