1.Preparation of Feasibility Study reply with the help of PI and study lead.2.Preparation of Investigator database3.Ethics Committee package preparation and submission, help in replying queries by EC.4.Assist in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures.5.Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents.6.Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit.7.CTA negotiation & Coordination with the legal team for legal implication on the CTA.8.Coordination with the central team for budget optimization9.Maintancae of monthly finance tracker10.Track different invoices as per study milestone achievement11.CRF, e-CRF entry, Data Query resolution.12. Help in Protocol specific sample collection & shipment of Lab samples and IP.12.Other Miscellaneous activities like documentation, record keeping, IP Accountability etc.13.Safety reporting of Clinical research participants and compile & submit CIOMS and Appendix XI.14.Ensuring documenting and following the process as per NABH standardsEducation :Msc., lifescience,nursing , B.Pharmacy/M.Pharmacy/ PharmD, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S, etc.) and lifescience graduates.Apply Now: HR Manager Ms. Saumya Only Whatsapp ur cv9346938942Role TraineeIndustry Type Medical, Healthcare, HospitalsEmployment Type Full Time, PermanentRole Category OtherEducationUG :B.Sc in Optometry, Bio-Chemistry, Biology, Microbiology, Nursing, Zoology, BAMS in Ayurveda, B.Pharma in PharmacyPG :M.Pharma in Pharmacy, MS/M.Sc(Science) in Nursing, Optometry, Zoology, Veterinary Science, Bio-Chemistry, Biology, Microbiology, MVSC in Veterinary Science
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