QREC Clinical Research Hiring Fresher Clinical Study Associate
- QREC Clinical Research Hiring Clinical Study Associate | Jaipur Life Sciences Jobs | Apply Now
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Qualification:
- Experience:
- Skills Required:
- Location & Salary
- Application Process
- Why Join QREC Clinical Research?
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this role?
- 2. Is prior experience required?
- 3. What is the job location?
- 4. What skills are important for this role?
- 5. What career growth can I expect?
- Summary Table
QREC Clinical Research Hiring Clinical Study Associate | Jaipur Life Sciences Jobs | Apply Now
QREC Clinical Research LLP is hiring Clinical Study Associates for its Jaipur location. This is a full-time, on-site opportunity for candidates from pharmacy and life sciences backgrounds who want to build a career in clinical research and clinical trials. The role focuses on study coordination, data management, and ensuring compliance with clinical protocols and regulatory standards.
This opportunity is ideal for freshers and early-career professionals looking to enter the clinical research industry, especially in roles related to clinical trials, data analysis, and regulatory compliance.
Company Overview
QREC Clinical Research LLP is a growing Contract Research Organization (CRO) with operations in India and the UAE, including offices in Jaipur, Hyderabad, and Dubai. The company provides end-to-end clinical research services such as Phase 3 & 4 clinical trials, real-world evidence studies, post-marketing surveillance (PMS), medical writing, clinical data management, and statistical analysis.
With over 450 completed projects, 180+ scientific publications, and 720+ medical writing assignments, QREC has established strong credibility in the clinical research space. The organization works with a large network of healthcare professionals and patients, contributing to improved healthcare outcomes and evidence-based medicine.
Job Role & Responsibilities
As a Clinical Study Associate, you will support the execution and monitoring of clinical trials while ensuring compliance with regulatory guidelines.
Key Responsibilities:
- Assist in coordination and monitoring of clinical trials (Phase 3 & 4 studies)
- Support preparation and maintenance of study documentation and trial records
- Liaise with investigators, healthcare professionals, and research teams
- Ensure compliance with study protocols, regulatory requirements, and GCP guidelines
- Assist in collection, verification, and analysis of clinical data
- Support clinical data management and reporting activities
- Maintain timelines and ensure smooth execution of multiple ongoing studies
This role contributes directly to the development of new therapies and evidence generation in healthcare.
Eligibility / Qualifications
Educational Qualification:
Candidates must have a degree in pharmacy or life sciences
Eligible courses include:
B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Pharmacology
Experience:
- Freshers and candidates with relevant internship/experience in clinical research can apply
Skills Required:
- Strong understanding of clinical trials and research methodologies
- Basic knowledge of healthcare practices and regulatory guidelines
- Familiarity with Good Clinical Practice (GCP) guidelines (preferred)
- Excellent communication and coordination skills
- Strong organizational and time management abilities
- Ability to handle multiple clinical studies simultaneously
- Basic knowledge of clinical data management and analysis
Location & Salary
- Job Location: Jaipur, Rajasthan (On-site)
- Job Type: Full-Time
- Department: Clinical Research
- Salary: As per industry standards (based on experience and skills)
This role offers strong career growth in clinical research, clinical trials management, and regulatory affairs.
Application Process
Interested candidates can apply through the official job link below:
Apply Here: https://www.linkedin.com/jobs/view/4393843089/
Ensure your resume highlights clinical research knowledge, internships, or project work related to clinical trials.
Why Join QREC Clinical Research?
- Work with an emerging CRO with global presence (India & UAE)
- Exposure to Phase 3 & 4 clinical trials and real-world studies
- Opportunity to contribute to scientific publications and research projects
- Strong learning environment for freshers in clinical research
- Career growth in clinical operations, data management, and regulatory affairs
This role is highly suitable for candidates looking to build long-term careers in clinical research and pharmaceutical development.
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with pharmacy or life sciences degrees, including freshers, can apply.
2. Is prior experience required?
No, freshers are eligible. However, internships or basic knowledge of clinical trials is beneficial.
3. What is the job location?
The role is based in Jaipur, Rajasthan.
4. What skills are important for this role?
Knowledge of clinical trials, GCP guidelines, and strong communication skills are important.
5. What career growth can I expect?
You can grow into roles such as Clinical Research Associate (CRA), Clinical Data Manager, or Regulatory Affairs Specialist.
Summary Table
| Category | Details |
|---|---|
| Company | QREC Clinical Research LLP |
| Vacancies | Clinical Study Associate |
| Required Education | B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research |
| Experience | Freshers / Entry-Level Candidates Eligible |
To apply for this job please visit www.linkedin.com.
