We are searching for a suitable candidate with one year experience in CRO under the department of Clinical operations/Clinical trials.
With willing to travel 60 to 70 % and perform the following activities independently.
1. Identify Potential investigators for study.
2. Responsible for identification and collection of necessary documents to be forwarded to project manager, in order to check feasibility of site/investigator and approval from authorities.
3. Able to perform alone Site Qualification visit and site initiation, conduct Monitoring visits and site close out visits.
4. maintaining a working copy of central investigator file and ensuring consistency with the site investigator file and a working record of all essential documents and reports.
5. Perform Source documents verification as per monitoring plan and other trial records are accurate, complete and up to date as per SOP.
6. Ensure timely collection of documents like CRF, DCF etc from the site along with SAE Reports in order to provide Biometerics/Licensing authority and others with the necessary documents.
7. Responsible for study updates and coordination with labs and other trial related services as per the study requirements.
8. Archival of study documents.
Salary: INR 2,50,000 - 3,00,000 .
Industry:Medical / Healthcare / Hospitals
Functional Area:Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category:R&D
Role:Clinical Research Associate/Scientist
Keywords:clinical research,clinical operations,clinical trials,site initiation,crf,project management,monitoring,cra,ich - gcp guidelines,site monitoring,clinical research associate,clinical trial associate
Experience : 0 - 2 Years
No. of Openings : 03
Education : B.Pharma, M.Pharma
Role : Clinical Research Associate
Industry Type : Pharma / BioTech / Clinical Research
Gender : [ Male / Female ]
Job Country : India
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Shri Misri Solutions Private Limited