Personal Information
Entreprise/Lieu de travail
Chennai Area, India India
Profession
6+yrs exp in Clinical Trial Operations actively looking opportunities in Chennai/Mumbai/Bengaluru/Hyderabad for CRA
Secteur d’activité
Medical / Health Care / Pharmaceuticals
À propos
A Quality-driven Clinical Researcher having more than 5 yrs experience in Clinical Operations. 2 yrs experience as CRA/Monitoring and 3 yrs experience as a CRC.
A Good verbal and written Communicator and Go Getter. Self Motivated, Adaptable and having an excellent attitude to learn new things.
As a CRA I have experience in Feasibility and Identification of the New Site and Investigator,Negotiation on Clinical Trial Agreement,EC Submission and Dossier Preparation,Subject Recruitment and Retention, Coordinating Agreements/Contracts with the Site,Conducting PSSV, SIV, IMV/RMV, SCV (Monitoring visits),Training the site for EDC (Oracle RDC, Inform and PheedIT) and IWRS and SAE/AE Reporting (...
J’aime
(5)Basic Six Sigma Presentation
vivekissar
•
il y a 13 ans
Risk Based Monitoring in Clinical Trials - Impact on Sites
Wool Consuting Group Inc.
•
il y a 9 ans
Risk Based Monitoring presentation by Triumph Research Intelligence January 2014
Triumph Consultancy Services
•
il y a 10 ans
eTMF in the fast lane
dirkbeth
•
il y a 12 ans
eTMF ppt
Ms.Chintan Wakade
•
il y a 8 ans
Personal Information
Entreprise/Lieu de travail
Chennai Area, India India
Profession
6+yrs exp in Clinical Trial Operations actively looking opportunities in Chennai/Mumbai/Bengaluru/Hyderabad for CRA
Secteur d’activité
Medical / Health Care / Pharmaceuticals
À propos
A Quality-driven Clinical Researcher having more than 5 yrs experience in Clinical Operations. 2 yrs experience as CRA/Monitoring and 3 yrs experience as a CRC.
A Good verbal and written Communicator and Go Getter. Self Motivated, Adaptable and having an excellent attitude to learn new things.
As a CRA I have experience in Feasibility and Identification of the New Site and Investigator,Negotiation on Clinical Trial Agreement,EC Submission and Dossier Preparation,Subject Recruitment and Retention, Coordinating Agreements/Contracts with the Site,Conducting PSSV, SIV, IMV/RMV, SCV (Monitoring visits),Training the site for EDC (Oracle RDC, Inform and PheedIT) and IWRS and SAE/AE Reporting (...