SIRO Clintech Pvt. Ltd. is a leading pharmaceutical and clinical research organization specializing in data management, biostatistics, and clinical trial solutions. With a commitment to innovation and accuracy, SIRO Clintech supports global clinical research projects, ensuring high-quality data integrity and regulatory compliance.
Job Description: Freelance Clinical Data Analyst
Key Responsibilities:
- Perform clinical data cleaning, validation, and discrepancy management for ongoing trials.
- Ensure CDISC (SDTM/ADaM) compliance and support database lock activities.
- Generate data listings, summaries, and reports for clinical study teams.
- Collaborate with biostatisticians, medical writers, and clinical research associates (CRAs).
- Adhere to ICH-GCP, FDA, and EMA guidelines for data integrity.
- Use EDC systems (Medidata Rave, Oracle Clinical, Veeva) for data review.
Skills Required:
✔ Strong knowledge of clinical trial data standards (CDASH, SDTM)
✔ Experience with SAS, SQL, or R for data analysis (preferred)
✔ Familiarity with MedDRA/WHODrug coding
✔ Attention to detail & ability to meet tight deadlines
Eligibility Criteria
✅ Education: Bachelor’s/Master’s in Life Sciences, Pharmacy, or Biostatistics
✅ Experience: Minimum 2 years in Clinical Data Management (CDM)
✅ Availability: Full-time (8 hours/day) for 3 months (remote work)
Benefits of Working with SIRO Clintech
- 💻 100% remote work – Flexible location
- ⏱️ Structured project timeline – Clear deliverables
- 🌍 Exposure to global clinical trials
- 📈 Networking with industry experts
How to Apply
Interested candidates should email their resume to:
📩 rashmi.palkar@siroclinpharm.com
