Experience in BA/BE studies.
Experience in monitoring & screening activities.
Experience in study document review.
Experience in monitoring of archival of data.
Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards.
To ensure compliance to Standard Operating Procedures (SOP).
To ensure compliance to the requirements of site procedures on Data integrity in GxP data handling.
As a Professional Assistant to VP RA, set up meetings, prepare presentations, co-ordinate for travel bookings, reimbursements and other activities required to…
Managing the day to day operational functions of the people service center to meet the defined SLA ,KPI's and Quality Standards.
The Director, Supply Chain will lead the supply chain team for the region, with the responsibility to execute all operational activities related to order…
Will be involved in statistical analysis of clinical data , inputs to protocol & Sample Size.
Major duties are he will be taking care of statistical analysis of…
To initiate improvement plans in existing assets, equipment and systems to improve safety, quality, reliability and cost.
16+ Yrs of work exp into API industry.
Coordination and oversight of Facilities Management (FM) services (Hard and Soft Services) at a site level, in accordance with the work plan and SOPs, with the…
Review Study protocol and Case Report Forms.
Preparation and review of DVS (Data Validation specification).
Preparation and review of eCRF Completion guidelines…
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