ICH Jobs in India

Bachelor s or master s degree in computer science or related field (advanced degree preferred). 12 years of experience as an enterprise architect in clinical regulatory compliance or safety within the pharmaceutical/healthcare industry. Strong understanding of global r More...

Bachelor s or master s degree in computer science or related field (advanced degree preferred). 12 years of experience as an enterprise architect in clinical regulatory compliance or safety within the pharmaceutical/healthcare industry. Strong understanding of global r More...

About the JobSkillsKnowledge of regulatory requirementsFDAAttention to detailStrong communication skillsProject managementAbility to work under pressureResearch skillsWe are hiring forSr. Executive Regulatory Affairs. Qualification: B.pharm/M.pharm Experience 2 to 5 years only Locat More...

Education: Bachelors degree or equivalent experience in a relevant field (e.g. Life Sciences Engineering Quality Management). Experience: Minimum of 3 years of experience in quality assurance within a regulated industry such as in the pharmaceutical biotechnology or medical device More...

Proactively identify issues and gaps in existing processes with minimal supervision and make the processes efficient with help of technology (SAS/R/Python codes dashboards) so that the results obtained are of high quality in quicker turnaround time; Develops algorithms for repetitive More...

Work Schedule Standard (MonFri) Environmental Conditions Office Job Description Discover Impactful Work: Thermo Fisher Scientific Inc. is seeking a highly motivated individual with a strong work ethic to join our team as a Clinical Trial Coordinator Level I. As a global leader in sci More...

Job Summary The Principal Medical Writer is an individual expert contributor capable of independently executing complex writing assignments involving a thorough understanding of clinical trial designs and interpretation of statistically analyzed research data. He/she would be expecte More...

Job Summary:Global Calcium is seeking a highly skilled Assistant Manager for our Quality Control department specifically focused on Active Pharmaceutical Ingredients (API). The ideal candidate will possess extensive experience in analytical method validation stability testing and comp More...

Years of Experience: 812 years Skill Set / Exposure: End to End Clinical Data Analysis and Reporting Project Management SAS R Programming CDISC Standards. Work Location: Bengaluru Responsibilities: Acts as key statistical programming contact for study related stakeholders and prov More...

Job Description: Accountability: Single point accountabilities and decisionmaking for your individual role should be agreed with your manager and captured in your MyPlan and Workday. Technical Expertise Scientific Leadership and Strategy: Acts as an internal expert for som More...

Job Description: Job Purpose: Provides medical/scientific expertise in the safety evaluation and risk management of key Client assets in clinical development and/or the postmarketing setting. Ensures scientifically sound review and interpretation of data and management of sa More...

Job Description: Job Purpose: Provides medical/scientific expertise in the safety evaluation and risk management of key Client assets in clinical development and/or the postmarketing setting. Ensures scientifically sound review and interpretation of data and management of sa More...

Job Description: Provide leadership to the Clinical Publishing team to align capabilities and priorities to business and operational needs of the organization (Priorities and resource management) Manage develop and optimize resources and operational activities to ensure coord More...

Alcon is looking to hire Statistical Programming who is responsible for driving productivity and accuracy relative to set strategies and objectives across the AGS regulatory operations team. Summary Of Position: Key contributor responsible for quality timely and cost efficient exec More...