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Senior Clinical Data Co-Ordinator

0-2 years
Not Disclosed
10 May 28, 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

 

Job Title: Senior Clinical Data Coordinator


Job Overview

We are looking for a Senior Clinical Data Coordinator to act as the primary Data Management point of contact for daily activities related to clinical studies. This individual will oversee study tasks, manage data processes, and ensure compliance with sponsor requirements and industry standards.


Key Responsibilities

  • Serve as the main point of contact for study-related Data Management activities

  • Oversee and coordinate tasks assigned to study team members

  • Provide training to new data management staff on processes and procedures

  • Plan, manage, and perform data processing activities in accordance with sponsor requirements

  • Author and review Data Management Plans (DMPs)

  • Design and review CRFs/eCRFs and participate in database design and UAT

  • Develop and test edit checks and data review listings

  • Monitor data quality and resolve discrepancies or queries

  • Assist in resolving coding discrepancies (medical history, AEs, procedures, and medications)

  • Validate captured data and generate clear, actionable queries

  • Collaborate with Quality Assurance during audits and provide real-time study monitoring reports

  • Specify and review edit check specifications for clinical databases

  • Maintain clinical trial documentation and support final archival processes

  • Conduct training for sponsors, sites, and internal staff on EDC and data quality processes

  • Lead recruitment-related activities such as interviewing and shortlisting candidates


Desirable Skills and Experience

  • Proven experience in Clinical Data Management

  • Strong understanding of data flow, EDC systems, and database validation

  • Familiarity with regulatory requirements and SOPs

  • Experience with CRF/eCRF design and database specifications

  • Strong leadership, problem-solving, and communication skills

  • Ability to train and mentor staff and participate in hiring processes