Are you an experienced clinical research professional seeking a rewarding career in risk-based monitoring? Novotech, a leading global CRO, is hiring Central Monitors in India. This role focuses on high-quality data monitoring, risk management, and patient safety in clinical trials.

Novotech offers a diverse, inclusive, and flexible work culture with global exposure in clinical research and biotech.

Key Responsibilities

As a Central Monitor at Novotech, you will:

• Plan and execute central monitoring in compliance with SOPs and GCP.
• Provide input into Integrated Quality Risk Management Plans (IQRMP).
• Collaborate with stakeholders for system setup and activation.
• Monitor patient, site, country, and project-level data using advanced analytics.
• Propose and manage signals, risks, and corrective actions.
• Document monitoring activities and maintain audit-ready records.
• Conduct outcome review meetings and ensure timely resolution of issues.
• Drive efficiencies in trial monitoring strategies by identifying trends.

Minimum Qualifications & Experience

• Education: Bachelor’s degree in Clinical, Life Sciences, Mathematics, Statistics, or related fields.
• Experience: 3+ years in clinical trials, or equivalent education and training.
• Skills Required:
  • Strong GCP and clinical trial knowledge.
  • Data analysis and risk identification skills.
  • Excellent communication and interpersonal abilities.
  • Ability to work independently and in cross-functional teams.
  • Problem-solving and multitasking capability.
  • Fluency in written and spoken English.

Benefits at Novotech

Novotech is committed to being an employer of choice. Benefits include:

• Flexible working options and wellness programs.
• Paid parental leave for both parents.
• Inclusive culture for all, including LGBTIQ+ and persons with disabilities.
• Career growth through ongoing development and global project exposure.
• Supportive leadership and collaborative teams.

How to Apply

Application Link