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Clinical Data Management

3-4 years
Not Disclosed
10 Feb. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Rewritten Description:

Position Title: Clinical Data Management
Location: Pune, India
Employment Type: Full-Time

Job Overview:
As a Clinical Data Manager, you will oversee the end-to-end delivery of data management services for single and multi-service projects with minimal guidance, ensuring that high-quality data management products are delivered on time, within budget, and to customer satisfaction. You will provide leadership to the Data Management (DM) team in areas such as project planning, execution, and close-out, and will also manage financial oversight for data management activities, communication, and milestone deliverables. The role includes responsibilities as a Data Team Lead (DTL).

Key Responsibilities:

  • Collect study setup requirements through effective communication with stakeholders.
  • Support and oversee the validation of new device integrations with minimal guidance.
  • Conduct regular data cleaning activities to ensure clean, accurate data and timely delivery to the sponsor.
  • Ensure that all deliverables meet customer expectations and quality standards.
  • Oversee service quality and ensure timelines and deliverables align with the agreed contract/scope of work (SOW).
  • Train and onboard new team members.
  • Lead internal study meetings, sponsor audits, and participate in study kick-off meetings.
  • Track project progress, identify risks, and take corrective actions as needed.
  • Manage the implementation of new technologies or database revisions.
  • Collaborate with the programming team to innovate and automate processes.
  • Maintain compliance with training and eSOP requirements.
  • Contribute to the development, revision, and maintenance of core operating procedures.
  • Foster collaborative communication with the Line Manager and cross-functional teams.
  • Perform other duties as directed by the Line Manager.

Required Qualifications:

  • Bachelor's degree in Pharmacy or equivalent (preferred).
  • 3-4 years of direct experience in Data Management, with at least 1 year as a CDM project lead (preferred).
  • Fluency in spoken English and advanced written English.
  • Proficiency in advanced computer applications such as Microsoft Excel, Word, and Outlook.
  • Advanced understanding of the drug development lifecycle and clinical research processes.

About IQVIA:
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. We accelerate the development and commercialization of innovative medical treatments to improve patient outcomes worldwide. For more information, visit
IQVIA Careers.