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Senior Clinical Data Associate

8-10 years
Not Disclosed
10 June 27, 2025
Job Description
Job Type: Hybrid 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

 

Senior Clinical Data Associate – Clinical Trials | Bangalore, Karnataka (Hybrid)

Job Summary:
Sitero is seeking an experienced Senior Clinical Data Associate to lead and manage clinical data management activities across early to late-phase trials. Based in Bangalore with a hybrid work model, this role is ideal for professionals with 8–10 years of clinical data management experience in CROs, pharma, or biotech. You'll be responsible for planning, execution, quality control, and client-facing leadership for global studies.


Key Responsibilities:

  • Lead all data management aspects from project setup to database lock

  • Create and review Data Management Plan, DVS, UAT scripts, SAE Reconciliation, etc.

  • Act as Lead Data Manager and liaise with sponsors and internal project teams

  • Coordinate and oversee data entry, cleaning, and data quality standards

  • Perform ongoing data review, edit checks, coding, and reconciliation activities

  • Provide project status updates and generate study metrics reports

  • Supervise, mentor, and train data management team members

  • Coordinate training and system access for CRAs, site staff, and stakeholders

  • Participate in eTMF audits and respond to regulatory feedback

  • Ensure compliance with CDISC SDTM, ICH-GCP, and SOP standards


Required Skills & Qualifications:

  • Life sciences graduate or equivalent (Bachelor’s/Master’s preferred)

  • 8–10 years of hands-on experience in Clinical Data Management in CROs/pharma/biotech

  • Proficient in EDC systems such as Medidata Rave; knowledge of JReview/Business Objects is a plus

  • In-depth understanding of CDISC, ICH-GCP, clinical trial protocol, and data standards

  • Strong project and stakeholder management skills

  • Excellent written and verbal communication skills

  • Working knowledge of Microsoft Office Suite (Word, Excel, PowerPoint)

  • Experience in supervising cross-functional teams and mentoring new joiners


Perks & Benefits:

  • Competitive salary and performance-based variable pay

  • Paid time off and comprehensive healthcare benefits

  • Retirement and insurance coverage

  • Hybrid work flexibility

  • Opportunities for cross-functional collaboration and career growth


Company Overview:

Sitero is a trusted provider of clinical services and technology solutions to the life sciences industry. We deliver excellence across clinical trials, data management, site payments, and software innovation, enabling life-changing therapies to reach patients faster with a strong focus on compliance and ethics.


Work Mode: Hybrid | Location: Bangalore, Karnataka
Compensation: Competitive salary with variable pay (exact figures not disclosed)


Apply Now

Take the next step in your clinical data management career. Join Sitero’s growing team of experts and help advance global clinical research. Apply today to lead meaningful projects in a dynamic, innovation-driven environment.