Nurse Practitioner Opening

Job Description

The clinical research associate will manage multiple aspects of the subjects welfare. You will conduct regular site visits, generate and distribute internal and external newsletters, prepare final reports, and liaise with interested parties regarding all trial aspects. You will play a leading role in generating and overseeing documentation and records.Clinical Research Associate Responsibilities:Creating and writing trial protocols, and presenting these to the steering committee.Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial.Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.Ordering, tracking, and managing IP and trial materials.Overseeing and documenting IP dispensing inventory, and reconciliation.Protecting subjects confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.Other DetailsSalary-30,000/- to 50,000/-Required Experience-0 To 10Minimum Age-18RequirementsQualification Required-Diploma,B.tech,M.tech,Bachelors degree in biological science or a related field.0 To 4 years of industry experience also can applyWork Department-Clinical Research AssociateWork Industry-PharmaceuticalSkills-Available to travel extensively and on short notice, and ability to manage travel schedules,for more clarification contact to this number-hidden_mobileAlso Send Your CV hidden_emailRegardsHR Placement Team

Keyskills :
nursingpharmaceuticspharmahealthcare