Life Science Job at Syneos Health
Looking for a high-growth life science job in clinical research and data monitoring? Syneos Health Careers brings an exciting opportunity for professionals to join as a Central Monitor in Hyderabad or Gurugram. This role is perfect for candidates seeking an opportunity for life science graduates to work in global clinical development, analytics, and patient-centered research environments.
About the Company
Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. With a presence across 110 countries and a workforce of over 29,000 employees, the company combines clinical, medical affairs, and commercial expertise to deliver impactful outcomes. Its Clinical Development model prioritizes both customer and patient, emphasizing innovation, agility, and collaboration to advance therapies and improve lives.
Job Details:
- Job Title: Central Monitor II / Senior Central Monitor
- Location: Hyderabad / Gurugram (Office-Based)
- Job Type: Full-Time
- Job ID: 25107211
- Company: Syneos Health
Role Overview
The Central Monitor II / Senior Central Monitor is responsible for centralized clinical data surveillance and analytics to ensure data quality, patient safety, and regulatory compliance. The role involves working closely with cross-functional teams to interpret clinical data, identify risks, and support study oversight through advanced monitoring techniques.
Key Responsibilities
- Collaborate with project teams and stakeholders during study development and maintenance in alignment with project plans
- Develop dashboards, tools, and custom reports for data oversight in collaboration with analytical teams
- Perform centralized data monitoring using analytics and signal detection methods such as QTLs, KRIs, and audit trail reviews
- Review and interpret study, site, and patient-level data including safety signals, efficacy trends, and protocol deviations
- Manage queries, listings, edit checks, and ensure compliance with reporting requirements
- Support Clinical Data Surveillance Leads with delegated tasks
- Identify risks proactively using predictive insights and contribute to process improvements
- Monitor site-level database readiness, timelines, and compliance metrics
- Support audit readiness and ensure adherence to regulatory standards across projects
- Participate in cross-functional meetings, data reviews, and risk discussions
- Perform additional assigned responsibilities as required
Candidate Profile
The ideal candidate demonstrates strong analytical capabilities, attention to detail, and the ability to interpret complex clinical datasets while working in a collaborative, fast-paced environment.
Educational Qualification
- Bachelor’s degree in Life Sciences, Health Sciences, or a related field
- Equivalent experience in clinical data management or centralized monitoring may be considered
Experience
- Minimum 1 to 3 years of relevant experience in clinical data management, centralized monitoring, or related areas
Key Skills & Competencies
- Knowledge of Good Clinical Practice (GCP) and clinical data principles
- Experience with tools such as CTMS, EDC systems, Spotfire, and data visualization platforms
- Strong analytical and problem-solving skills
- Experience in signal detection methodologies (QTLs, KRIs, SAE review, etc.)
- Familiarity with data and vendor reconciliation processes
- Experience in user acceptance testing and validation of outputs
- Effective cross-functional communication and multitasking abilities
