Novotech has announced an opening for a Clinical Lead Analyst (CLA) in Bangalore, India. This opportunity is suitable for clinical research professionals interested in clinical trial operations, study oversight, clinical analytics, CTMS, EDC, protocol deviation management, and project performance monitoring.
As a global full-service Contract Research Organization (CRO), Novotech supports biotechnology and clinical research programs across multiple international markets. The Clinical Lead Analyst will work closely with the Clinical Lead to monitor clinical deliverables, project timelines, study quality, risks, compliance, and site performance.
Novotech Clinical Lead Analyst Job Overview
| Details | Information |
|---|---|
| Company | Novotech |
| Position | Clinical Lead Analyst (CLA) |
| Job ID | 4362 |
| Location | Bangalore, Karnataka, India |
| Job Type | Full Time |
| Industry | Clinical Research / CRO |
| Experience | Minimum 3 years |
| Relevant Experience | Minimum 1.5 years in CRO/clinical research or equivalent |
| Posted Date | August 19, 2026 |
Key Responsibilities
As a Clinical Lead Analyst at Novotech, the selected candidate will support the Clinical Lead throughout the clinical trial lifecycle. Key responsibilities include:
- Provide clinical analytics, reports, project status updates, risk alerts, and mitigation recommendations.
- Support oversight of clinical project deliverables and ensure adherence to protocol, SOPs, study plans, and applicable regulations.
- Review project KPIs periodically and provide status and performance analysis.
- Follow up on outstanding project action items as directed by the Clinical Lead.
- Monitor study-level site performance and recommend appropriate corrective actions.
- Support monitoring of clinical study quality and protocol compliance.
- Maintain effective project and site-level communication with relevant stakeholders.
- Ensure appropriate compliance and maintenance of clinical study databases.
- Work with systems such as Clinical Trial Management System (CTMS), Interactive Web Response System (IWRS), and Electronic Data Capture (EDC).
- Support the Clinical Lead with protocol deviation management.
- Perform administrative and project execution activities assigned by the Clinical Lead.
- Support clinical activities during study start-up, maintenance, and close-out.
Qualifications and Experience
Candidates interested in the Novotech Clinical Lead Analyst job should meet the following requirements:
- Minimum 3 years of overall work experience.
- At least 1.5 years of relevant experience in a Clinical Research Organization (CRO), clinical research environment, or equivalent role.
- Basic knowledge of ICH-GCP and applicable clinical research regulations, local laws, and guidelines.
- Knowledge of Microsoft applications, particularly Excel, Word, and PowerPoint.
- Exposure to basic data analysis used during clinical trial start-up, maintenance, and close-out.
- Understanding of clinical trial operations and project performance monitoring.
- A certification course in Clinical Research will be an added advantage.
Note: The job description does not specify a mandatory academic degree. Candidates should assess their eligibility against the experience, clinical research knowledge, and skill requirements stated by Novotech.
Key Skills
Candidates with knowledge or experience in the following areas may be well aligned with this Clinical Lead Analyst opportunity:
Clinical Research | Clinical Trial Operations | ICH-GCP | CTMS | EDC | IWRS | Clinical Analytics | KPI Monitoring | Site Performance | Protocol Deviations | Risk Management | Clinical Quality | Study Start-Up | Study Close-Out | Microsoft Excel
Why Consider This Opportunity?
Novotech operates as a global full-service CRO with offices across Asia-Pacific, the United States, and Europe. According to the employer’s job description, employees may have access to:
- Flexible working options
- Paid parental leave
- Flexible leave entitlements
- Wellness programs
- Professional development programs
- Mentorship opportunities
- Exposure to global clinical research projects
- Collaborative and inclusive work environment
Who Should Apply?
This opportunity may be particularly relevant to professionals currently working in areas such as clinical trial operations, clinical project support, clinical research coordination, site management support, clinical analytics, or CRO study operations who meet Novotech’s experience requirements.
Because the position requires at least 3 years of work experience, including 1.5 years of relevant clinical research/CRO experience, this is not positioned as a fresher role.
How to Apply
