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Clinical Data Analyst I/Ii

0-2 years
₹4.5 – ₹7 LPA
10 July 19, 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

Location: Serilingampalli, Telangana (Remote)
Position: Clinical Data Analyst I/II
Experience Required: Entry-level to 2+ years in clinical data management
Company: Parexel

About Parexel:
Parexel is a leading global clinical research organization providing the full range of Phase I to IV clinical development services to help life sciences companies bring innovative therapies to market. With a focus on quality, compliance, and patient safety, Parexel partners with clients to advance healthcare worldwide.

Role Overview:
Parexel is hiring Clinical Data Analysts (CDA I/II) to join their Clinical Data Management (CDM) team. The role involves supporting data cleaning, validation, documentation, and compliance activities for global clinical trials. Ideal for individuals looking to start or grow their career in clinical research data.

Key Responsibilities:

1. Data Validation & Cleaning:

  • Perform and/or begin to lead query management and manual/SAS listing reviews.

  • Support external data reconciliation processes and database lock activities.

2. Documentation & Setup:

  • Assist in setting up data management documentation: CRF Completion Guidelines, Protocol Deviation Specs, and Data Validation Specs.

  • Maintain Trial Master File (TMF) accuracy and SOP compliance.

3. User Acceptance Testing (UAT) & Study Start-Up:

  • Perform or begin leading user acceptance testing for clinical database setup.

  • Support protocol and EDC screen reviews during study initiation.

4. Data Entry & Tracking:

  • Review CRFs and support data entry as needed.

  • Ensure timely updates and tracking of data entries.

5. Compliance & Quality:

  • Adhere to ICH-GCP guidelines, Parexel SOPs, and regulatory requirements.

  • Support functional QC activities during patient data review and database setup.

6. Training & Development:

  • Stay compliant with assigned training roles and participate in on-the-job training.

  • Address development goals with a focus on learning and adaptability.

Candidate Requirements:

  • Bachelor’s degree in Life Sciences, Pharmacy, or related fields.

  • Basic understanding of clinical data flow and validation concepts.

  • Familiarity with CDMS tools like InForm, Rave, Veeva, Datalabs, or ClinBase.

  • Basic knowledge of medical terminology and coding dictionaries (e.g., MedDRA, WHODRUG).

  • Good problem-solving, time management, and communication skills.

  • Strong team collaboration with a flexible, learning-focused mindset.

  • Fluent written and spoken English.

What We Offer:

  • Remote work flexibility with exposure to global clinical projects.

  • Structured learning path for early-career data professionals.

  • Collaborative team culture and professional growth environment.

  • Competitive compensation with benefits.

Estimated Salary: ₹4.5 – ₹7 LPA (based on early-career clinical data roles in Telangana with remote setup)