We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials. 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.

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-30,000/- to 75,000/-

Required Experience-0 To 4

Minimum Age-18

Responsibilities:

Qualification Required-Diploma,B.tech,M.tech,12th,All Gradtuate

Bachelors degree in biological science or a related field.

Work Department-Quality,Production,testing,Research

Work Industry-Pharmaceuticals,Pharma

Skills-Ability to manage and prioritize workload effectively.

for more clarification contact to this number-9217672140

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Regards

HR Placement Team

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