Clinical Research Associate I/II
Clinical Research Associate I/II
IQVIA
Job description
Looking to build a career in clinical trial monitoring? Explore this CRA 1/2 role at IQVIA in Thane.
Company Description
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. The company works with life sciences and healthcare industries to speed up the development and launch of new medical treatments. IQVIA creates intelligent connections that help improve patient outcomes and population health worldwide. The company continues seeking diverse talent committed to innovation and real world impact.
Job Summary
This hybrid role is based in Thane, within IQVIA's clinical monitoring team. As a CRA 1/2, you will monitor and manage assigned sites to make sure studies are run correctly and data is reported as required. Your work will include site visits, subject recruitment support, and protocol training. The role also involves tracking study progress and maintaining accurate site documentation throughout each trial.
Key Responsibilities
Carry out site visits, including selection, initiation, monitoring, and close out visits.
Follow GCP and ICH guidelines during every site visit.
Work with sites to plan and track subject recruitment for each study.
Train site staff on the protocol and keep regular contact with sites.
Check that site practices follow the protocol and required regulations.
Flag quality issues to the right people when they come up.
Track regulatory approvals, enrollment, CRF completion, and data query resolution.
Support study start up activities when needed.
Keep site documents ready for the Trial Master File.
Make sure the Investigator's Site File stays complete and compliant.
Write clear visit reports, follow up letters, and other required documents.
Work closely with the study team to support smooth project delivery.
Help plan subject recruitment for specific sites, where applicable.
Support site level financial matters and invoice collection, where applicable.
Educational Qualification
Bachelor's degree in a scientific or healthcare field is preferred.
Skills Required
At least 1 year of on site monitoring experience.
Good knowledge of GCP and ICH guidelines.
Basic therapeutic and protocol knowledge, gained through company training.
Comfortable using Microsoft Word, Excel, and PowerPoint, along with a laptop, iPhone, and iPad.
Good written and spoken English.
Strong organizing and problem solving skills.
Good time management and basic financial management skills.
Ability to build strong working relationships with coworkers, managers, and clients.
Salary Strucure
The average salary for a Clinical Research Associate (CRA 1/2) at IQVIA in India ranges from ₹7.2 Lakhs to ₹12.4 Lakhs per year.
Career Development
This role gives you hands on experience in clinical trial monitoring within a large global research company. IQVIA also supports steady growth through training, mentoring, and clear paths to move into more senior CRA roles.
How to Apply
Visit our job portal and search for the CRA 1/2 role in IQVIA.
Click on the job posting to read all the details about the job.
Fill in your details. Upload your updated resume.
Send your application.
Education
Bachelor's Degree
Key Skills
Market insights & trends
Salary Insights
The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.
Hiring Trends
The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.