Novartis Hiring 2022 Degree for Clinical Research Associate At Navi Mumbai, IN . Novartis Notification full details below..Interested and eligible candidates can Apply Now.
- Vacancy details:
- Post Name: Clinical Research Associate
- Qualification: Degree
- Experienced:Up to 2 years
Job Description: Novartis Hiring For Clinical Research Associate !
- Important Details :
- Location: Navi Mumbai, IN
- Post of date: 09/04/2022
- Selection Process: The selection will be on the basis of Interview.
Job Overview
Your responsibilities:
Your responsibilities include, but are not limited to:
Allocation, initiation and conduct of trials
• Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial. Is the frontline liaison between Novartis and sites to ensure successful collaboration, meeting Novartis expectation on milestone and deliveries
• Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and Novartis procedures. Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate
• Conducts continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety. Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions.
• Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.). Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements. Attends onboarding-, disease indication and project specific training and general CRA training as required
• Documents monitoring activities appropriately following Novartis standards. Collaborates with the CRA Group Head/CSM to ensure recruitment plans and execute contingency plans, as needed. Participates from audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines. Performs additional task as assigned
Delivery of quality data and compliance to quality standards
• Monitors studies as per current legislations, ICH/GCP and Novartis standards. Ensures timely delivery, of high quality, robust and reliable data of the monitored sites to support the goals of Trial Monitoring as defined by Trial Monitoring. (ADIS, DBL). Identifies issues at sites; resolves issues and escalate as appropriate
• Collaborates with internal stakeholders and site personnel to manage data query resolution process to ensure timely and accurate data entry. Ensures the site Investigator Folder is up to date. Is responsible for collecting essential documents from site and accountable to keep sTMF(s) current. Supports the implementation of innovative processes and technologies
Budget and productivity
• Negotiates investigator remuneration; prepares financial contracts between Novartis and investigational sites and investigators. Ensures that payments are appropriately triggered to investigational sites
Minimum requirements
What you’ll bring to the role:
• Degree in scientific or healthcare discipline.
• Up to 2 years pharmaceutical industry experience or other relevant experience
• Good knowledge of drug development process specifically clinical trial/research
• Knowledge of international standards (GCP/ICH, FDA, EMEA)
• Monitoring experience is desirable
Important for the role:
• Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.
• A minimum of 50% overnight travel may be required.
How to Apply :
Step 1: Click on below link and you will be redirected to Career Page of Recruiting Company or Career portal.
Step 2. Register on Career Page of the Company or Career Portal by giving log in credentials and other personal or education details .
Step 3.Upon successful registration .User need to log in with credentials.
Step 4.Once logged in, User need to fill the all relevant personal ,educational , Work experience details ,attach resume and submit application form.
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