Clinical Data Manager / Clinical Data Reviewer (Lab Safety & Coding)

Clinovo
πŸ‘œ 4 - 6 years
πŸ“ Remote
πŸ’Ό Remote
πŸ’° Not Disclosed
Posted on May 12, 2026

Job Description:

πŸš€ WE’RE HIRING – Clinical Data Manager / Clinical Data Reviewer (Lab Safety & Coding) πŸš€

Clinovo is actively hiring experienced Clinical Data Management professionals for a remote opportunity in the Pharmaceutical / CRO / Clinical Research domain. This role is ideal for candidates with strong expertise in clinical data review, lab safety review, coding activities, and clinical trial data integrity.

🏒 Company: Clinovo 
🌐 Website: Clinovo

πŸ‘‰ Role: Clinical Data Manager / Clinical Data Reviewer (Lab Safety & Coding) 
πŸ’Ό Experience: 4–6 Years 
πŸ“ Location: Remote 
🧾 Job Type: Full-Time 
🏒 Industry: Pharmaceutical / CRO / Clinical Research 

πŸ’₯ Job Summary: 
We are looking for a detail-oriented Clinical Data Manager / Data Reviewer to support clinical trial data quality and integrity. The role involves performing comprehensive data reviews, handling lab and safety data, supporting coding activities, and contributing to study conduct and closeout activities.

πŸ”§ Key Responsibilities: 
⭐ Clinical Data Review: 
β€’ Conduct clinical data reviews to ensure accuracy, completeness, and consistency of trial data 
β€’ Perform ongoing data cleaning and discrepancy management 
β€’ Generate, track, and resolve data queries 

⭐ Lab & Safety Review: 
β€’ Perform local lab data review to identify inconsistencies and outliers 
β€’ Conduct safety data review including Adverse Events (AE) and related data 
β€’ Ensure alignment with protocol and clinical standards 

⭐ Coding Activities: 
β€’ Execute medical coding review and reconciliation 
β€’ Work with MedDRA and WHO Drug coding dictionaries 
β€’ Ensure accurate coding of adverse events and concomitant medications 

⭐ Study Conduct & Closeout: 
β€’ Support study conduct activities including ongoing data review and cleaning 
β€’ Assist in database lock and closeout activities 
β€’ Ensure data readiness for analysis and reporting 

πŸ›  Required Skills & Qualifications: 
β€’ Bachelor’s degree in Life Sciences, Pharmacy, or related field 
β€’ 4–6 years of experience in Clinical Data Management / Data Review 
β€’ Strong experience in data review, query management, and discrepancy handling 
β€’ Knowledge of lab data and safety data review processes 
β€’ Experience in medical coding (MedDRA, WHO Drug) 
β€’ Familiarity with EDC systems such as Medidata Rave and Oracle Clinical 
β€’ Understanding of clinical trial processes and GCP guidelines 

🎯 Preferred Skills: 
β€’ Experience in database lock and closeout activities 
β€’ Knowledge of edit checks and validation processes 
β€’ Basic exposure to SAS / SQL / data listings review 

πŸ’‘ Soft Skills: 
β€’ Strong attention to detail 
β€’ Analytical thinking and problem-solving 
β€’ Good communication and coordination skills 
β€’ Ability to manage timelines and work independently 

✨ Why Join Clinovo? 
β€’ Opportunity to work remotely with global clinical research teams 
β€’ Exposure to advanced clinical data management and safety review activities 
β€’ Strong career growth opportunities in CDM and Clinical Research 
β€’ Collaborative and quality-focused work environment 
β€’ Opportunity to work on global clinical trials and regulatory-compliant processes 

πŸ“© Apply Now: 
Interested candidates can share their updated resume directly with the recruitment team.

Submite your CV 
πŸ“© bhavanasri.gundala@clinovo.com

πŸ’¬ Join WhatsApp Group: 
πŸ‘‰ Join Now

⚑ Join Clinovo and contribute to high-impact global clinical research projects while advancing your expertise in Clinical Data Management, Safety Review, and Coding.

Key Responsibilities:

⭐ Clinical Data Review:
Conduct clinical data reviews to ensure accuracy, completeness, and consistency of trial data
Perform ongoing data cleaning and discrepancy management
Generate, track, and resolve data queries
βœ” Verified