| Job alert | Jobs 21 - 25 of 25 |
Sr. Business Analyst - Pharma/Biotech
Evalueserve India
–
Gurugram, Haryana, India
... requirements, identify the right sources for data gathering and execute delivery of assigned task with high quality Experience handling industry standard public databases/ data sources like Clinicaltrials.gov, Pubmed, FDA website, EMA website; ... - Apr 23
Azure Integration Service
SAM Manpower and Career Services LLP
–
Sector 46, Uttar Pradesh, 201303, India
₹2000000.000 - ₹3400000.000 per annum
... development of business models Experience coordinating projects is a plus Experience working with regulated environments (FDA, G*P, HIPAA, etc.) is a strong plus but not required Certifications within the Microsoft stack are a plus, but primarily ... - Apr 25
CRP (Franchise Medical Lead) - Obesity / Diabetes
Lilly
–
Sector 56, Haryana, 122003, India
... laws, guidance (for example, FDA, ICH, and CPMP etc.), Good Clinical Practices (GCPs), company standards, Lilly policies and procedures, global quality standards, the Principles of Medical Research and activities are aligned with the medical vision. ... - May 07
Regulatory Compliance Specialist
Wadhwani AI
–
Delhi, India
SUMMARY As a Regulatory Compliance Specialist, you are required to oversee compliance with FDA, ISO, and EU regulations. Develop and implement strategies, conduct audits, and produce quality documentation. Furthermore, provides recommendations for ... - May 14
Similar
Bhavyansh Infotech
–
Ansari Nagar East, Delhi, 110029, India
Not Specified
... Key responsibilities and skills may include, but are not limited to: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS. Develop ADaM, specifications and ... - May 21