IQVIA is hiring!
1. Centralized Monitoring Assistant (Multiple)
Location: Bengaluru/Thane/Kochi
Required: B Pharm or M Pharm freshers with good communication skills and knowledge in Clinical Research.
2. Safety Specialist (Home Based) (Multiple)
Required: Minimum 2 years in Clinical Trial case processing (ICSR), Argus experience is preferred.
3. Senior Safety Specialist (Home Based) (Multiple)
Required: Minimum 2 years in Clinical Trial case processing (ICSR), along with 5+ years in Pharmacovigilance, Argus experience is preferred.
4. Clinical Data Coder 1 (Bengaluru/Thane) (Multiple)
Required: Clinical Coding with MedDRA AND WHO DD with 2 years of relevant experience.
5. Centralized Monitoring Coordinator (Bengaluru) (Multiple)
Required: Lifescience graduate with a minimum 1 year of Clinical Research or Clinical Domain experience
6. Associate Manager Centralized Monitoring (Bengaluru) (Single)
Required: Bachelor's degree in Clinical, Lifescience with a minimum of 7 years of relevant work experience or equivalent combination of education, training with minimum 1 year of LM experience. Excellent communication, interpersonal, people leadership skills, project management skills and coaching skills. Experienced in Risk-Based Monitoring and client-facing roles
7. Regulatory Affairs Manager (Bengaluru/Thane/Kochi/Pune)
Assists with the delivery of Safety and Regulatory services according to ICH GCP guidelines, regulatory requirements and IQVIA Biotech SOPs and/or project-specific procedures.
Primary responsibilities include review, preparation and submission of regulatory safety reports (including expedited and periodic) to all applicable Regulatory Authorities, Ethics Committees, Institutional Review Boards (IRBs) and Investigators with defined timelines.
8. Senior Regulatory Affairs Specialist (Home Based)
Required: 5 to 7 years of relevant experience. Key skills: Global submission, FDA submissions (Initial IND submissions), Initial CTA submissions, Lifecycle management of INDs, CTAs, etc., CMC, Authoring/Preparing of regulatory submission/documents, CRO experience would be desirable
9. Regulatory Affairs Officer 2 (Bengaluru)
Required: Minimum 5 years of Medical/Scientific writing experience with an understanding of US Regulatory. Should have excellent communication skills.
10. Medtech Technical Writer (Bengaluru)
Required: Bachelor's degree in Lifescience related discipline or related field. Familiarity with structural and content requirements of Clinical investigation plans, Clinical study reports and similar documents.
Interested candidates can send their CV to uttamrao.shinde@gmail.com before 13 October 2021
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