To be successful in this role, you should be able to recognize logistical problems and initiate appropriate solutions. Ideal candidates will be detail-oriented, have the ability to multitask, and be able to collaborate with various role players.
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.
Other Details
Salary-20,000/- to 41,000/-
Required Experience-0 To 5
Minimum Age-18
Qualification Required-A Nursing degree.Diploma,Bachelors degree in pharmacy or pharmacology.
Work Department-Clinical Research
Work Industry-Hospitality,Pharma
Skills-Excellent verbal and written communication skills.
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Regards
HR Placement Team
Keyskills: healthcare consulting patient communications healthcare management patient care nursing healthcare