Etico Research Pvt Ltd Released Job Openings On 18/07/2022.Etico Research is a Contract Research Organization (CRO), headquartered in United States of America, with hands on experience and expertise offering clinical trial services to pharmaceutical, biotech and medical device companies for Phase II-IV, registration and post-marketing trials. Etico Research combines scientific and clinical leadership with expert trial delivery to create distinctive world-class solutions.
Vacancy Details:
Etico Research Pvt Ltd Recruiting B.Pharma,B. Sc,M. Sc M.Pharma Graduates with 00-02+Years Experience for Clinical Research Associate Position.Complete Details for the Clinical Research Associate as follows.
Important Details :
- Location :Hyderabad/Secunderabad (WFH during Covid)
- No of Vacancies:Not Disclosed By Recruiter
- Details of Salary:Not Disclosed By Recruiter
- Opening date for online Application: 18/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
- Feasibility analysis, identification, and selection of Potential Investigators (PI).
- Planning the conduct of the clinical trial and developing trial management systems.
- Prepare documents for ethics committee submissions.
- Planning and coordination of investigator meetings (IM) and prepare presentation materials.
- Management of recruitment strategies when necessary.
- Management and preparation of tracking documents.
- Management of study drug/supply/equipment delivery, shipment, inventory, and accountability.
- Create documents required by the project team prior to the start of the study (e.g. feasibility questionnaires, patient tracking tools etc.,)
- Prepare, plan, organize and conduct pre-study (site selection) visits and report on these visits to Project Manager (PM) to assist in site selection.
- Prepare, plan, organize and conduct site initiation visits.
- Collect and review essential documents from study sites.
- Monitor the conduct of clinical trial as per protocol at multiple sites.
- Prepare, plan, organize and conduct the monitoring and close out visit as required.
- Establishment and maintenance of good clinical data collection practices to ensure validity of studies.
- Prepare, plan, organize and assist for an audit as required.
- Waivers and SAE management in association with Medical Monitor.
- Overall site responsibility, Central Lab coordination.
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