Parexel Hiring Senior Clinical Research Associate
Are you an experienced clinical research professional eager to contribute to cutting-edge clinical trials and improve patient outcomes worldwide? Parexel, a leading global biopharmaceutical services organization, is hiring for the position of Senior Clinical Research Associate (CRA). This remote role based in Bangalore offers a dynamic work environment, challenging projects, and the opportunity to work on life-changing research. Parexel Hiring Senior Clinical Research Associate
If you have a strong background in clinical research and a passion for advancing healthcare, this is the perfect opportunity for you!
About Parexel
Parexel is a globally recognized contract research organization (CRO) dedicated to improving global health through clinical research and regulatory consulting. The company collaborates with top pharmaceutical, biotech, and medical device companies to bring innovative therapies to market. Parexel Hiring Senior Clinical Research Associate
With a commitment to patient-centric research, quality, and compliance, Parexel provides an environment that fosters professional growth and work-life balance while delivering groundbreaking medical solutions.
Position: Senior Clinical Research Associate
📍 Location: Remote – Bangalore
📅 Application Deadline: February 14, 2025
🎓 Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc in Life Sciences
💼 Experience Required: 4 – 7 years
✅ Job Type: Verified Job | Online Application
Key Responsibilities
As a Senior Clinical Research Associate, you will be responsible for managing clinical trial sites from start-up to close-out, ensuring compliance with protocols, regulations, and industry standards. Your role will include:
1. Study Start-Up Phase:
- Serve as the primary point of contact for clinical trial sites.
- Conduct feasibility studies and site qualification visits.
- Assist in contract negotiations and site initiation processes.
- Prepare and submit regulatory documents (IRB/IEC and MoH/RA applications).
- Develop site activation strategies and ensure timely patient recruitment.
2. Trial Maintenance & Monitoring Phase:
- Oversee ongoing compliance with study protocols and regulatory requirements.
- Conduct on-site and remote monitoring visits.
- Address site-related issues, including data quality, training deficiencies, and non-compliance.
- Maintain accurate and updated documentation in Clinical Trial Management Systems (CTMS).
3. Study Close-Out Phase:
- Evaluate site performance and ensure study-related activities are completed.
- Manage study supplies, site payments, and regulatory documentation.
- Prepare sites for audits and regulatory inspections.
Skills & Qualifications Required
✔ Experience: Strong background in site management or clinical research, with a thorough understanding of clinical trial methodology.
✔ Educational Qualification: Degree in Biological Sciences, Pharmacy, or Life Sciences (or equivalent experience).
✔ Technical & Soft Skills:
- Strong problem-solving and decision-making abilities.
- Excellent communication and interpersonal skills.
- Proficiency in CTMS, MS Office, and regulatory documentation.
- Ability to work independently as well as in a team.
- High attention to detail and a commitment to quality.
Why Join Parexel?
🌍 Global Impact: Play a key role in developing therapies that improve patient lives.
📈 Career Growth: Opportunities for mentorship, training, and professional development.
🤝 Collaborative Environment: Work with experts across the globe in a dynamic setting.
🏡 Work-Life Balance: Enjoy the flexibility of a remote work arrangement.
🔒 Job Security & Benefits: Competitive salary, insurance, and employee wellness programs.
How to Apply?
If you’re interested in this exciting opportunity, apply online today! The deadline for applications is February 14, 2025.
Start your journey with Parexel and make a meaningful impact in the field of clinical research! 🚀 Parexel Hiring Senior Clinical Research Associate
More Jobs