Clinical Research Associate Hiring at ICON
Key Highlights of the Clinical Research Associate Job at ICON Plc
| Feature | Details |
|---|---|
| Job Title | Clinical Research Associate (CRA) |
| Company | ICON Strategic Solutions |
| Location | Mumbai & Delhi |
| Salary Range | ₹4.8 – ₹6 Lacs per annum |
| Experience Required | Minimum 2 years of onsite monitoring experience in oncology |
| Educational Qualification | B.Pharm, M.Pharm, Pharm D, BDS, or MBBS |
| Key Skills | Oncology expertise, communication, problem-solving, attention to detail, time management |
| Work Highlights | Work/life balance, flexibility, collaboration, time management |
| Application Process | Online |
Embark on a Rewarding Career as a Clinical Research Associate at ICON Plc
ICON Strategic Solutions, the world’s largest and most comprehensive Clinical Research Organization (CRO), offers an exciting opportunity for experienced Clinical Research Associates (CRAs) in Mumbai and Delhi. Join a global leader dedicated to healthcare intelligence and innovation, where your work contributes to groundbreaking research and life-saving treatments.
Why Choose ICON Strategic Solutions?
A Global Leader in Clinical Research
With its robust global presence, ICON Strategic Solutions is synonymous with excellence in clinical research. The organization thrives on collaboration and innovation, empowering its team members to make a meaningful difference in healthcare. Clinical Research Associate Hiring at ICON
Work-Life Balance and Flexibility
ICON understands the importance of personal well-being. This role offers flexibility and a supportive environment, ensuring you can maintain a healthy work-life balance while excelling in your career.
Growth Opportunities
Whether it’s through mentorship, collaboration, or exposure to cutting-edge projects, ICON equips its employees with tools and resources for continuous professional development.
Your Role as a Clinical Research Associate
As a CRA, you will play a pivotal role in overseeing clinical trials and ensuring they adhere to the highest standards of quality and compliance. Here’s what the role entails:
Site Selection and Initiation
You’ll take the lead in identifying and setting up study sites. This includes verifying that sites have the necessary resources, infrastructure, and approvals to start clinical trials seamlessly.
Monitoring Visits
Conduct routine visits to ensure that site activities align with study protocols and regulatory requirements. Your vigilant monitoring will ensure the collection of accurate and reliable data.
Study Site Management
Maintain high-quality data collection and reporting at each site. By minimizing errors and ensuring compliance, you’ll contribute to the success of every clinical trial.
Team Collaboration and Support
Your experience will be invaluable in mentoring team members, helping them navigate challenges and deliver exceptional results. As a CRA, you’ll foster a culture of collaboration and mutual support. Clinical Research Associate Hiring at ICON
Are You the Right Fit?
Qualifications
To excel in this role, you must have:
- A degree in B.Pharm, M.Pharm, Pharm D, BDS, or MBBS.
- At least 2 years of onsite monitoring experience in oncology clinical trials (excluding training and induction).
Key Skills
- Oncology Expertise: Familiarity with protocols for cancer treatments and monitoring processes.
- Attention to Detail: Ability to analyze and interpret data with precision, ensuring compliance with regulatory standards.
- Communication: Strong verbal and written communication skills to effectively interact with stakeholders.
- Problem Solving: Proactively address challenges and find effective solutions to maintain trial integrity.
- Time Management: Efficiently manage site activities and prioritize tasks to meet deadlines. Clinical Research Associate Hiring at ICON
What Makes This Job Stand Out?
Impactful Work
Every task you perform as a CRA contributes directly to advancing healthcare and saving lives. Your expertise will play a critical role in delivering life-changing therapies to patients worldwide.
Collaborative Environment
ICON fosters a supportive and collaborative culture, where team members work together to achieve shared goals. You’ll have the chance to learn from industry leaders and share your own expertise.
Verified Opportunity
This is a verified job posting, ensuring that you’re applying for a legitimate and rewarding career path with one of the top names in clinical research.
How to Apply
Interested candidates can apply online. If you meet the qualifications and are ready to make a significant impact in clinical research, this role is for you. Take the next step in your career by joining ICON Strategic Solutions as a Clinical Research Associate.
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