Parexel, a global leader in clinical research and biopharmaceutical services, has announced multiple job openings across its India locations — especially Bengaluru. These roles span Clinical Operations, Central Data Review, Site Contracts, and Global Project Management, making this a strong opportunity for candidates aiming to grow in the clinical research and pharmaceutical sector.
If you’re looking for Parexel jobs in India, clinical research openings, or pharma careers with global exposure, this consolidated job update covers all available positions, eligibility criteria, and application instructions.
🔹 Available Parexel Job Openings
Below are all the roles included in this article:
- Clinical Operations Manager – Bengaluru
- Senior Data Surveillance Analyst (Central Data Review) – Bengaluru
- CDA Manager / Site Contract Associate II – Bengaluru
- Specialist, Global Site Management (Project Specialist I/II) – Bengaluru
Let’s break them down one by one.
1. Clinical Operations Manager – Parexel, Bengaluru
Responsibilities
- Lead end-to-end Clinical Operations project activities
- Manage clinical teams and ensure on-time delivery
- Oversee project quality, timelines, and regulatory compliance
- Support resource planning, project oversight, and sponsor communication
- Mentor and develop clinical operations staff
- Participate in audits, process improvements, and business development
Qualifications
- Life sciences / pharmacy / medical / nursing degree
- Strong experience in Clinical Operations or Monitoring
- Excellent leadership and communication skills
- Good understanding of ICH-GCP, CTMS, EDC systems
2. Senior Data Surveillance Analyst (Central Data Review) – Parexel
Responsibilities
- Lead Risk-Based Quality Management (RBQM) activities
- Develop & maintain Data Surveillance Plans
- Configure tools like CluePoints for statistical monitoring
- Detect data trends, anomalies & quality risks
- Collaborate with Clinical, Data Management & Quality teams
- Create Central Monitoring Reports & present findings
Qualifications
- 5+ years of clinical data / RBQM / central monitoring experience
- Strong analytical mindset; basic SAS skills preferred
- Knowledge of SDTM, GCP, and clinical data standards
- Life sciences, statistics, pharmacy, or related degree
3. CDA Manager / Site Contract Associate II – Parexel
Responsibilities
- Draft, negotiate & manage clinical site contracts
- Handle budget reviews, amendments, and timelines
- Ensure legal compliance with local/global laws
- Coordinate with sites, legal team & project stakeholders
- Maintain documentation and support study startup
Qualifications
- 2–5 years experience in site contracting
- Strong negotiation & legal interpretation skills
- Excellent written & verbal communication
- Degree in Law, Business, Life Sciences or Pharma
4. Specialist, Global Site Management (Project Specialist I/II)
Responsibilities
- Support project leads with planning and tracking
- Maintain project management plans, dashboards & metrics
- Assist with vendor documentation, training, setup
- Monitor system access, team lists & compliance
- Document project activities across lifecycle
Qualifications
- Prior experience in project support or clinical operations
- Good Excel & project management tool skills
- Life sciences or business background preferred
- Good communication & coordination skills
💼 Benefits of Working at Parexel
- Global exposure in world-class clinical research
- Career development & structured training
- Competitive salary packages
- Work with experienced scientific & medical teams
- Opportunity to impact global drug development
📌 How to Apply
Application Link for Clinical Operations Manager – Bengaluru
Application Link for Senior Data Surveillance Analyst (Central Data Review) – Bengaluru
Application Link for CDA Manager / Site Contract Associate II – Bengaluru
Application Link for Specialist, Global Site Management (Project Specialist I/II) – Bengaluru
