Clinical Research Associate at IQVIA
A rare opportunity through IQVIA Careers India has emerged for aspiring Clinical Research Associates in Thane, India. IQVIA is seeking qualified candidates for a full-time, hybrid role that promises to enhance their career in the life sciences sector. Interested applicants are encouraged to apply before the deadline.
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization is dedicated to creating intelligent connections to accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health worldwide.
Job Details:
- Location: Thane, India
- Job Type: Full-time
- Work Model: Hybrid
- Reference Number: R1557317
IQVIA Careers India: Job Description
In this IQVIA careers India role, the selected candidate will perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Key Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive, and track subject recruitment plans in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
- Ensure copies/originals (as required) of site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator’s Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports, generating follow-up letters, and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Eligibility Criteria for IQVIA Careers India
- Bachelor’s Degree in a scientific discipline or healthcare preferred.
- Requires at least 1 year of on-site monitoring experience.
- Equivalent combination of education, training, and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., GCP and ICH guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in Microsoft Word, Excel, PowerPoint, and use of a laptop computer and iPhone/iPad (where applicable).
- Written and verbal communication skills including a good command of the English language.
- Organizational and problem-solving skills.
How to Apply
Additional Information
IQVIA is committed to integrity in the hiring process and maintains a zero-tolerance policy for candidate fraud. All information and credentials submitted in applications must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of the application or termination of employment if discovered later, in accordance with applicable law. The organization appreciates honesty and professionalism.
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This IQVIA careers India opportunity presents a significant chance for qualified candidates to advance their careers in clinical research. Interested individuals are encouraged to apply at the earliest to secure their position in this dynamic field.



