1-2

You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments

These services are essential for regulatory compliance and successful trial outcomes. They often utilize specialized software and systems to manage the data efficiently.A critical phase in clinical research that assures collection, integration and availability of data at appropriate quality and cost.

Knowledge of Dispensing in warehouse of Raw Material & Packing Material. Manage daily production QMS activities (deviations, OOS/OOT investigations, CAPA, change control) with proficiency in PowerPoint, Excel, Al tools & knowledge of manufacturing process

APDM Pharmaceuticals Private Limited has its office in Ahmedabad with all QA and regulatory support staffs for managing CDO and CDMO projects,vendor Audits, BA BA monitoring, project and Engg team.

ITI / Diploma for Operators (Sterile USFDA Exp.) B.Pharm / M.Pharm for Officer (Sterile USFDA Exp.)

To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information

In this role you are required to solve routine problems, largely through precedent and referral to general guidelines

Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts, Clinical Research Associate at Sun Pharma

o2h group seeds new ideas in science, technology and green innovation. We work across boundaries and take a collaborative and shared approach to innovation, and therefore we co-invest, co-create and co-execute to bring these ideas to life.