About Bio-Prospera Clinical Research
Bio-Prospera Clinical Research is a leading Global Contract Research Organization (CRO) based in Mumbai, Maharashtra, India. We specialize in end-to-end clinical trials services, supporting comprehensive drug development and product lifecycle management. Our clients include pharmaceutical, biotechnology, medical device, and government organizations.
Walk-in Drive Details
Venue: Plot 44, Viraj Industrial Estate, Gokhiware Village, Chinchpada, Golani Naka, Vasai East, Palghar
Date: 27 August to 29 August
Time: 10 AM to 1 PM
Open Positions
- Clinical Research Associate (CRA)
- Clinical Operation Manager (COM)
Eligibility Criteria
- Educational Qualification: Life Science Graduate / B. Pharm / M. Pharm
- Experience: Minimum 1 year
- Work Type: Office-based
Key Responsibilities
Clinical Research Associate (CRA)
| Responsibility | Description |
|---|---|
| Investigator Recruitment | Participate in the recruitment process, perform site initial visits, and evaluate site capabilities. |
| Study Start-up Activities | Work with site staff to obtain regulatory approvals and prepare for study initiation. |
| Study Initiation | Review protocols, regulatory issues, and provide training on eCRF and monitoring activities. |
| Training | Train site staff on the EDC system and verify site computer systems. |
| Site Audits | Conduct periodic site file audits to ensure compliance with GCP and SOPs. |
| GCP Compliance | Ensure adherence to Good Clinical Practices (GCP), investigator integrity, and compliance with study procedures. |
| Documentation | Document clinical trial materials, perform inventory checks, and ensure proper handling of unused materials. |
| Data Quality | Review and verify clinical data through electronic CRF and on-site source verification, resolve queries. |
| Protocol Review | Review protocols, eCRF, and study manuals as requested by the Clinical Trial Manager. |
| Primary Contact | Serve as the primary contact between the company and the investigator, coordinate correspondence, and ensure timely data transmission. |
| Final Data Review | Assist with final data review, query resolution, and study close-out visits. |
| Investigator Meetings | Assist and attend Investigator Meetings for assigned studies. |
Clinical Operation Manager (COM)
| Responsibility | Description |
|---|---|
| Site Management | Oversee site activities, ensure compliance with clinical trial protocols, and manage site performance. |
| Operational Oversight | Coordinate operational aspects of clinical trials, including resource allocation and budget management. |
| Team Leadership | Lead and manage the clinical operations team, ensuring effective execution of study protocols. |
| Regulatory Compliance | Ensure all clinical operations adhere to regulatory requirements and GCP. |
| Stakeholder Communication | Act as the primary liaison between the CRO and stakeholders, including sponsors and regulatory authorities. |
| Risk Management | Identify and manage risks associated with clinical trials and implement mitigation strategies. |
How to Apply
Interested candidates are invited to attend the walk-in drive or send their applications to zabiulla.m@pfizer.com.
Why Join Bio-Prospera?
- Innovative Environment: Work with cutting-edge clinical research technologies.
- Career Growth: Opportunities for professional development and advancement.
- Impactful Work: Contribute to global healthcare improvements through clinical research.
For more information about Bio-Prospera Clinical Research, visit our website.
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