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Central Monitor (India)

1+ years
Not Disclosed
10 Jan. 30, 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

📢 Now Hiring: Central Monitor - India 🇮🇳

💼 Position: Central Monitor
🏢 Industry: CRO - Clinical Operations
📍 Location: Home-based (India)
Job Type: Full-time

🔎 Job Overview

Innovaderm is looking for a Central Monitor to provide centralized statistical reviews of clinical trial data. This role involves using analytics and statistical methods to identify emerging risks and ensure data integrity throughout the study lifecycle. As part of a risk-based monitoring strategy, the central monitor helps maintain the quality of clinical trial data.

🔑 Key Responsibilities

1. Data Review & Risk Identification

  • Review clinical trial data (operational and subject data) using various tools and systems in alignment with the centralized monitoring plan
  • Identify trends indicating systematic errors and potential performance issues at study/country/site levels
  • Document the results of reviews according to established procedures
  • Track and communicate emerging risks with support from senior team members

2. Support & Collaboration

  • Assist the Central Monitoring team in performing high-quality, on-time reviews
  • Contribute to risk characterization and reporting
  • Support review set-up activities and maintain department databases

3. Data Quality & Monitoring

  • Share responsibility for ensuring data quality across study, country, and site levels
  • Participate in the analysis and review of clinical data, identifying trends and ensuring accurate documentation

📌 Requirements

🎓 Education:

  • Bachelor's degree in a field relevant to clinical research

🛠 Experience:

  • Minimum of 1 year of experience in central statistical monitoring and 6 years in clinical monitoring, data management, or other relevant areas
  • Basic understanding of statistical monitoring and Risk-Based Quality Management (RBQM)
  • Knowledge of clinical trial database systems (EDC, IRT, CTMS, etc.)
  • Familiarity with descriptive analysis (means, medians, significance)
  • Involvement in clinical data analysis and review

💻 Skills:

  • Proficiency in MS Office (Word, Excel, PowerPoint)
  • Ability to prioritize tasks and manage workloads
  • Strong communication skills in English
  • Good understanding of project protocols and clinical trial processes

🎯 Perks & Benefits

Permanent full-time position
Flexible work schedule
Vacation benefits
Home-based position
Ongoing learning and development

📌 Company: Innovaderm (Specialized in Dermatology CRO Research)

📩 Apply Now!