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Associate Clinical Data management at SDC

Published on

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Engineering

Hyderabad

1 - 3 Years

Verified Job

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Looking to build a strong career in clinical data management jobs in India? Here’s an excellent opportunity for life science and pharmacy graduates. SDC (Statistics & Data Corporation) is hiring for the role of Associate Clinical Data Manager in Hyderabad (Hybrid).

This role is ideal for candidates with experience in clinical trials, EDC systems, CRF design, and data management lifecycle activities, offering exposure to global CRO operations.


πŸ“Œ Job Overview

  • Position: Associate Clinical Data Manager
  • Company: SDC (Statistics & Data Corporation)
  • Location: Hyderabad, Telangana (Hybrid)
  • Job Type: Full-Time
  • Industry: Clinical Research / CRO / Data Management

πŸ§ͺ Key Responsibilities

As an Associate Clinical Data Manager, you will be responsible for end-to-end clinical data management activities:

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Study Setup & Design

  • Design and review CRFs (Case Report Forms)
  • Develop database structures and annotations
  • Perform EDC setup, validation checks, and testing

Study Conduct

  • Manage query resolution and data listings review
  • Handle data transfers and quality checks
  • Ensure compliance with ICH-GCP and regulatory guidelines

Study Closeout

  • Support database lock activities
  • Maintain high-quality data and documentation standards

Project & Team Support

  • Assist in managing timelines, budgets, and deliverables
  • Mentor junior Clinical Data Associates
  • Collaborate with cross-functional teams and clients

🎯 Required Qualifications

Educational Criteria

  • Master’s degree (Life Sciences / Pharmacy / Engineering) + 1+ year experience, OR
  • Bachelor’s degree + 3+ years clinical trials experience,

Key Skills

  • Strong knowledge of clinical trials & data management lifecycle
  • Hands-on experience with EDC systems
  • Expertise in:
    • CRF design
    • Query management
    • Data validation
  • Familiarity with:
    • ICH-GCP, FDA/CFR guidelines
    • Medical coding review
  • Tools: MS Office, MS Project

πŸ’° Salary (Expected Range)

  • β‚Ή5.5 LPA – β‚Ή9.5 LPA (Estimated)
    (Based on industry standards for 1–4 years CDM experience in CROs)

🌟 Why Join SDC?

  • Work with a global CRO (since 2005)
  • Exposure to international clinical trials
  • Strong career growth & promotion opportunities
  • Flexible hybrid work model
  • Competitive benefits + work-life balance
  • Innovation-driven culture with clinical technology focus

πŸ“ Job Location

  • Hyderabad, Telangana, India (Hybrid Work Model)

πŸš€ How to Apply

Application Link

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