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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:
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- 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
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