Public Health Job Opportunity at Parexel | Apply now for a Remote role
Looking for a high-impact public health job in clinical research? Parexel is hiring a Site and Monitoring Health Lead for a remote position in India. This role plays a critical part in safeguarding clinical trial quality, ensuring regulatory compliance, and strengthening site oversight in multinational studies. If you have strong monitoring experience and want to explore rewarding Parexel jobs with remote flexibility, this opportunity could be the perfect fit.
Job Details:
- Job Position: Site and Monitoring Health Lead
- Company: Parexel
- Category: Clinical Trials
- Location: India (Remote)
- Job ID: R0000038570
About the Company:
Parexel is a globally recognized Clinical Research Organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies in developing innovative therapies. Known for its expertise in clinical trials and regulatory excellence, Parexel offers dynamic Parexel jobs across global markets. The company emphasizes quality, compliance, and patient-focused research, making it a strong choice for professionals seeking long-term growth in clinical research and public health.
Job Description:
This remote job focuses on ensuring high-quality clinical trial oversight and monitoring effectiveness. The SMH Lead will conduct site risk analysis, monitoring visit report reviews, sponsor oversight visits, and data spot checks. The role requires implementing Study Specific Oversight Plans (SSOPs) and ensuring alignment with Risk Management Plans (Risk MAP). The candidate will use a risk-based approach to review critical-to-quality items and maintain an “inspection ready at all times” mindset. The position also supports inspection preparation and regulatory compliance.
Qualifications:
- Bachelor’s Degree required
- Master’s in Public Health (MPH) preferred
Knowledge and Experience:
- Significant direct monitoring experience with a CRO or pharmaceutical company
- Experience in multinational clinical studies
- Lead CRA/management experience preferred
- Experience across Phase I–III clinical trials
- Experience in prevalent and rare medical conditions preferred
- Previous audit and regulatory inspection experience preferred
Key Responsibilities:
Oversight of Monitoring Effectiveness
- Implement oversight encounters, including site risk analysis, site contacts, aggregate data review, monitoring visit report review, Sponsor Oversight Visits, system/data spot checks, and periodic summaries
- Ensure timely documentation and filing of oversight activities
- Complete Sponsor Oversight Visit reports consistently on time and with good quality
- Create or follow Study Specific Oversight Plans (SSOPs)
- Utilize innovative approaches to solve issues impacting clinical site delivery
- Conduct root cause analysis and recommend corrective actions
- Support inspection preparation and management
Collaborative Relationships
- Work independently and collaboratively with cross-functional teams
- Build relationships with investigators and site staff
- Identify potential sites for new studies
- Support less experienced investigator sites
- Align SSOP with Risk MAP and assess site outliers
Operational Responsibilities
- Implement the Site and Monitoring Health strategy aligned with ICH-GCP regulations
- Lead oversight and trend meetings with study teams and CROs
- Stay updated with global and local regulatory requirements
