skillindiajobs
Register for Job
Hyderabad Jobs
Banglore Jobs
Chennai Jobs
Delhi Jobs
Ahmedabad Jobs
Mumbai Jobs
Pune Jobs
Vijayawada Jobs
Gurgaon Jobs
Noida Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Clinical research associate-reputed clinical research company

2.00 to 5.00 Years   Mumbai City   18 Mar, 2022
Seven Consultancy
Job LocationMumbai City
EducationNot Mentioned
SalaryNot Disclosed
IndustryRecruitment Services
Functional AreaSales / BD
EmploymentTypeFull-time

Job Description

    SALARY: 4 to 5 LPA VACANCIES: 3 QUALIFICATION: At least a Bachelor s Degree in medicine MALE/FEMALE: Both EXPERIENCE: 2-5 years JOB DETAILS One of our clients, a reputed company in clinical research, is looking out for a Clinical Research Associate for their office based in Mumbai. The job responsibilities are as follows: 1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 2. Facilitate preparation and collection of site level documents. 3. Participate in trial site training activities, as assigned. 4. Perform monitoring visits according to monitoring plan, as assigned, including source document verification. 5. Facilitate site drug supply management. 6. Co-ordinate site level updates of technical systems (ClinAdmin, EDC). 7. Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc). 8. Demonstrate and apply GCP and ICH requirements. 9. Prepare study monitoring reports under supervision, as appropriate. 9.Assist with data query resolution process (both at Site and in-house with Data Management). 10. Perform Site Closeout activities. 11. Under the guidance of Senior CRA/CRA Group Head perform IM related activities like logistics, preparation of IM binders and technical presentations. 12. Assist with preparation of required regulatory submission liaising with DRA team. ,

Keyskills :
gcpclinical researchclinical trialsdocumentationsiteclinical data managementclinical datadata managementquery resolutionstudy monitoringclinical developmentconstruction planningclinical study

APPLY NOW

Clinical research associate-reputed clinical research company Related Jobs

© 2020 Skillindia All Rights Reserved