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Central Monitor (India/China)

0-2 years
Not Disclosed
10 Sept. 25, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Central Monitor (India/China)

Location: Bangalore, India – Ground Floor, Unit 1, Block E, Helios Business Park, 560103
Job ID: 3421
Schedule: Full-time
Posting Date: 19 September 2025
Apply Before: 14 October 2025, 06:30 PM


Company Overview

Novotech is a global full-service Clinical Contract Research Organization (CRO):

  • Headquartered in Sydney, Australia, with 34 offices across Asia-Pacific, North America, and Europe.

  • Employs over 3,000 employees and partners with 5,000+ clinical sites.

  • Offers services across all clinical trial phases and therapeutic areas, including:

    • Feasibility assessments

    • Ethics and regulatory submissions

    • Data management & statistical analysis

    • Medical monitoring & safety solutions

    • Central lab services

    • Report writing to ICH requirements

    • Project & vendor management

  • Certified with ISO 27001 (Information Security) and ISO 9001 (Quality Management).


Role Overview

The Central Monitor is responsible for risk-based clinical trial monitoring using patient data and site/country/project-level information. The role focuses resources on critical risks impacting data quality and patient safety and involves centralized, remote, and on-site monitoring activities.


Minimum Qualifications & Experience

  • Education: Bachelor’s degree in Clinical, Life Sciences, Mathematics, Statistics, or related field.

  • Experience: Minimum 3 years in clinical trials or equivalent combination of education, training, and experience.

  • Skills & Knowledge:

    • Strong understanding of GCP and clinical trial processes

    • Risk identification and trend analysis

    • Data analysis and technical skills in clinical trials

    • Good interpersonal and communication skills (English – written & oral)

    • Ability to work independently and as part of a team

    • Strong problem-solving and multitasking capabilities


Key Responsibilities

Central Monitoring & Risk Management

  1. Plan central monitoring activities per SOPs and GCP guidelines.

  2. Provide input into the Integrated Quality Risk Management Plan (IQRMP).

  3. Support setup and activation of central monitoring systems.

  4. Monitor patient data, site/country/project-level data, and quality metrics centrally.

  5. Identify risks and propose actions for signal and issue management.

  6. Track action items and ensure timely closure with relevant teams.

  7. Communicate significant non-compliance or critical issues to stakeholders.

  8. Support overall efficiency in clinical trial monitoring strategies.

Documentation & Reporting

  1. Document centralized monitoring activities accurately.

  2. Facilitate and attend central monitoring outcome review meetings.

  3. Provide timely reports on findings, risks, and action resolutions to stakeholders.

Stakeholder Collaboration

  1. Work with cross-functional teams to implement centralized monitoring strategies.

  2. Ensure coordination between internal and external stakeholders for risk mitigation.


Team & Culture

  • Strategic vs. transactional mindset with ability to make proactive decisions.

  • Collaborative, inclusive culture where all voices are valued.

  • Support from senior leadership for professional growth.

  • Work alongside empowered teams committed to clinical trial excellence.


Equal Opportunity Statement

Novotech is an Equal Employment Opportunity Employer, committed to diversity and inclusion. Employment decisions are based on merit, qualifications, and business requirements, without regard to race, religion, gender, age, sexual orientation, disability, or other protected characteristics.