IQVIA Hiring SSU CRA (Site Start-Up Clinical Research Associate)

IQVIA Hiring SSU CRA in Thane | Clinical Research Associate Jobs

IQVIA has announced recruitment for the position of SSU CRA (Site Start-Up Clinical Research Associate) in Thane, India. This is an excellent opportunity for clinical research professionals with onsite monitoring experience who are looking to build careers in clinical operations, site management, healthcare research, and global clinical trials.

The company is hiring candidates with at least 1 year of onsite monitoring experience and strong knowledge of Good Clinical Practice (GCP), ICH guidelines, clinical trial regulations, and site management activities.

This hybrid work opportunity is ideal for professionals interested in clinical trial monitoring, healthcare analytics, pharmaceutical operations, regulatory compliance, clinical data management, and healthcare research programs.

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About IQVIA

IQVIA is one of the world’s leading healthcare technology and clinical research organizations providing advanced solutions in clinical trials, healthcare analytics, pharmaceutical consulting, healthcare intelligence, and life sciences research.

The company works closely with pharmaceutical companies, biotechnology firms, healthcare institutions, and medical device organizations to support global clinical development and healthcare innovation.

IQVIA is recognized for its expertise in clinical operations, healthcare technology, regulatory services, clinical data management, biostatistics, and medical research support.

Working at IQVIA provides professionals exposure to international clinical trials, advanced healthcare systems, global research teams, and pharmaceutical development programs.

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SSU CRA Vacancy Details

Position

SSU CRA (Clinical Research Associate)

Job Type

Full-Time

Work Model

Hybrid

Job ID

R1541674

Location

Thane

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Job Role and Responsibilities

Selected candidates will manage clinical trial monitoring and site management activities to ensure compliance with study protocols, regulatory requirements, and sponsor expectations.

Key Responsibilities

• Perform site selection, initiation, monitoring, and close-out visits
• Ensure compliance with Good Clinical Practice (GCP) and ICH guidelines
• Support subject recruitment and enrollment tracking activities
• Conduct protocol and study-related training for sites
• Monitor study site quality and protocol adherence
• Track regulatory submissions and study approvals
• Manage case report form (CRF) completion and query resolution
• Maintain Trial Master File (TMF) and Investigator Site File (ISF) documentation
• Prepare monitoring visit reports and follow-up letters
• Coordinate with clinical operations teams and study stakeholders
• Support site financial management and invoice tracking if applicable

Candidates with experience in clinical operations, healthcare compliance, clinical data review, pharmacovigilance support, healthcare analytics, and medical documentation may have an added advantage.

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Eligibility and Qualifications

Candidates applying for this IQVIA Clinical Research Associate role should possess strong clinical research knowledge and monitoring experience.

Required Qualification

B.Pharm, M.Pharm, PharmD, MSc Clinical Research, MSc Biotechnology, MSc Life Sciences, BSc Nursing, MBBS, Bachelor’s Degree in scientific or healthcare disciplines.

Experience Required

Minimum 1 year of onsite clinical monitoring experience.

Required Skills

• Strong understanding of GCP and ICH guidelines
• Knowledge of clinical trial regulations and monitoring processes
• Experience in site management and study coordination
• Good communication and documentation skills
• Organizational and problem-solving abilities
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Ability to work with clinical research teams and stakeholders

Professionals with expertise in clinical trial management, healthcare operations, medical writing coordination, healthcare analytics, and pharmaceutical compliance are encouraged to apply.

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Location and Salary

Location

Thane

Salary

The estimated salary for SSU CRA and Clinical Research Associate roles generally ranges between ₹5 LPA and ₹10 LPA depending on monitoring experience, therapeutic expertise, and clinical trial exposure.

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How to Apply

Interested candidates can apply through the official IQVIA careers portal using the application link below:

https://jobs.iqvia.com/en/jobs/R1541674-0

Candidates should ensure all educational details, monitoring experience, and professional information are accurate before applying.

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Frequently Asked Questions

What experience is required for this IQVIA CRA role?

Candidates must have at least 1 year of onsite monitoring experience.

What is the work model for this position?

The role follows a hybrid work model.

What qualifications are preferred?

Candidates with pharmacy, life sciences, biotechnology, nursing, or clinical research backgrounds are preferred.

What is the location for this role?

The position is based in Thane.

What is the expected salary range?

The estimated salary range is ₹5 LPA to ₹10 LPA depending on experience and clinical trial expertise.

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IQVIA SSU CRA Recruitment Overview

Company	IQVIA
Department Vacancies	SSU CRA / Clinical Research Associate
Qualification	B.Pharm, M.Pharm, PharmD, MSc Clinical Research, MSc Biotechnology
Experience	Minimum 1 Year Monitoring Experience
Location	Thane

Tagged as: Pharma Jobs in Mumbai