Position: Centralized Monitoring Analyst (12-month contract)
Location: Remote - India-based
The Company: A pioneering global pharmaceutical company
Role Overview:
Join a leading organization recognized as a pioneer in the pharmaceutical industry, known for their innovative research and contributions to global healthcare. This remote position based in India supports centralized clinical trial monitoring for this US-based client, ensuring the highest standards of data quality and integrity.
Key Responsibilities:
1. Conduct centralized monitoring of clinical trial data to identify discrepancies and maintain data quality.
2. Utilize CluePoints and Spotfire programming tools for advanced data analysis, risk detection, and signal management.
3. Collaborate with cross-functional clinical teams to resolve data queries and ensure regulatory compliance.
4. Support clinical data management activities including query resolution and SAE reconciliation.
5. Generate analytic reports and presentations to support data-driven decisions.
Required Skills and Experience:
6. 3-5 years of experience in centralized monitoring within clinical research.
7. Proficiency in CluePoints and Spotfire programming is essential.
8. Strong programming background and analytical skills are highly desirable.
9. Solid understanding of clinical trial data management and Good Clinical Practice (GCP) guidelines.
Qualifications:
10. Professional certification in Clinical Data Management (e.g., CCDM) is advantageous.
11. Degree in Pharmacy, Life Sciences, or equivalent is advantageous.
Contract Details:
12. Duration: 12 months (extendable)
13. Location: Remote (India-based)
This is an excellent opportunity for skilled clinical data professionals to advance their career with a market-leading pharmaceutical innovator. Candidates with strong centralized monitoring experience and expertise in CluePoints and Spotfire are encouraged to apply.