Centralized Clinical Trial Manager
- Bangalore, Chennai, Bengaluru
- ICON Full Service & Corporate Support
- Clinical Trial Management
- Office or Home
Talent Acquisition Business Partner
- Full Service Division
About the role
Centralized Clinical Trial Manager
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Centralized Clinical Trial Manager to join our diverse and dynamic team. As a Centralized Clinical Trial Manager at ICON, you will play a crucial role in overseeing the centralized monitoring activities of clinical trials, ensuring the smooth coordination of data-driven insights to enhance trial quality and patient safety. You will contribute to the advancement of innovative treatments and therapies by managing centralized trial activities and collaborating with cross-functional teams to ensure study compliance and efficiency.
Location: Bangalore or Chennai ( Home Based or Office Based)
What You Will Be Doing:
- Leading the centralized monitoring activities for clinical trials, including data review and risk-based monitoring.
- Collaborating with Clinical Operations, Clinical Trial Management and Project Management teams to identify potential monitoring risks and ensuring proactive escalation of monitoring issues.
- Ensuring study compliance with regulatory requirements and protocols by overseeing real-time data reviews and monitoring activities.
- Providing oversight on site performance, patient safety, and data quality through focused monitoring data insights and analytics.
- Coordinating with cross-functional teams to ensure efficient execution of clinical trials and contribute to continuous improvement in trial processes.
Your Profile:
- Bachelor’s degree in life sciences, healthcare, or a related field (advanced degree preferred).
- Minimum 8-10 years of Clinical Research experience with at-least 5 years of on-site monitoring experience.
- Experience in On-Site Monitoring and Clinical Trial Management, with a solid understanding of on-site monitoring approaches.
- Strong analytical skills with proficiency in clinical trial data review and interpretation.
- Excellent organizational and project management skills, with the ability to manage multiple studies and meet deadlines.
- Effective communication and interpersonal skills, with the ability to collaborate across diverse teams and functions.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
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