Apply for Clinical Trial CRA at Advity, Hyderabad
- Clinical Trial CRA – B.Pharm / M.Sc | Advity | Hyderabad
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Work Type
- Application Process
- Why Join Advity?
- FAQs
Clinical Trial CRA – B.Pharm / M.Sc | Advity | Hyderabad
Apply for Clinical Trial CRA at Advity, Hyderabad. B.Pharm/M.Sc/Pharm.D graduates with 2-4 years clinical research experience welcome.
Advance your career in clinical research and CRA operations with Advity, a trusted organization committed to integrity and quality in clinical trials. As a Clinical Trial CRA in Hyderabad, India, you will play a pivotal role in managing, monitoring, and ensuring compliance and efficiency across all phases of clinical studies.
Company Overview
Advity Research is a leading clinical research organization (CRO) that specializes in conducting high-quality clinical trials and supporting the pharmaceutical and biotechnology sectors. Our mission is to deliver reliable, accurate, and compliant clinical data to accelerate the development of life-changing therapies.
With a team of dedicated professionals and experienced CRAs, Advity has established a strong reputation for quality, integrity, and ethical clinical research practices. We focus on innovation, collaboration, and continuous learning, ensuring every team member contributes to advancing healthcare solutions.
Job Role & Responsibilities
As a Clinical Trial CRA, you will be responsible for site monitoring, study compliance, and regulatory adherence to ensure the success of clinical trials.
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits in accordance with GCP guidelines.
- Ensure study protocols, SOPs, and regulatory requirements are followed at all sites.
- Collaborate with clinical teams, investigators, and site staff to maintain trial quality and compliance.
- Review and verify source documents, CRFs, and regulatory documents.
- Identify and report adverse events or protocol deviations in a timely manner.
- Maintain accurate and up-to-date site documentation and trial records.
- Support audit and inspection readiness and facilitate regulatory inspections.
- Provide guidance and training to site staff on study procedures and compliance.
This role is ideal for professionals seeking high CPC clinical research careers, CRA positions, and roles in clinical trial monitoring.
Eligibility / Qualifications
- Educational Qualification: B.Pharmacy, M.Sc, Pharm.D, or M.Pharmacy.
- Experience: 2–4 years in clinical research, site monitoring, and trial coordination.
- Skills:
- Strong knowledge of GCP, ICH guidelines, and clinical trial regulations.
- Excellent communication, documentation, and interpersonal skills.
- Ability to manage multiple trial sites and maintain compliance.
- Fluency in English.
Preferred Courses: B.Pharm, M.Pharm, MSc Clinical Research, Pharm.D, Life Sciences, Biotechnology.
Location & Work Type
- Location: Hyderabad, India
- Job Type: Full-Time, On-Premise
Advity provides a professional environment promoting career growth, skill development, and a collaborative work culture.
Application Process
Take the next step in your high CPC clinical research career:
📧 Send your resume to: hr@advityresearch.com
Join a company dedicated to quality, compliance, and integrity in clinical trials.
Why Join Advity?
- Work with a reputable CRO in India impacting clinical research globally.
- Gain experience in CRA monitoring, trial coordination, and regulatory compliance.
- Be part of a dedicated and collaborative team focused on ethical and high-quality clinical research.
- Develop your career in clinical research, site management, and clinical operations.
- Contribute to advancing healthcare and pharmaceutical innovation.
FAQs
Q1: Who can apply for this position?
B.Pharm, M.Sc, Pharm.D, or M.Pharmacy graduates with 2–4 years of clinical research experience.
Q2: What is the work mode?
Full-time, on-premise in Hyderabad, India.
Q3: What are the key responsibilities?
Monitoring trial sites, ensuring GCP compliance, protocol adherence, and regulatory documentation.
Q4: How can I apply?
Email your resume to hr@advityresearch.com.
Q5: Is fluency in English required?
Yes, to effectively communicate with sites and teams.
Call to Action:
Advance your career in clinical trial monitoring and CRA operations. Apply now to join Advity and contribute to high-quality, compliant clinical research.
| Company | Advity Research |
|---|---|
| Vacancies | Full-Time, On-Premise |
| Required Education | B.Pharm, M.Sc, Pharm.D, M.Pharmacy, MSc Clinical Research, Life Sciences, Biotechnology |
| Experience | 2–4 years in clinical research, site monitoring, trial coordination |
| Location | Hyderabad, India |
To apply for this job email your details to hr@advityresearch.com
