Live opening · Posted 8 hours ago

Clinical Study Manager II

ICON Strategic Solutions · Bengaluru, Karnataka, India (Hybrid)
Linkedin Hybrid
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At a glance

The key details from the original listing.

Posted 8 hours ago
CompanyICON Strategic Solutions
LocationBengaluru, Karnataka, India (Hybrid)
Work modeHybrid
SourceLinkedin
Listed8 hours ago

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About the role

Description supplied by the original job listing.

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Clinical Study Manager II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key Responsibilities Include
Lead the planning, execution, and monitoring of complex clinical trials, ensuring adherence to regulatory requirements and project timelines.
Collaborate closely with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of advanced clinical studies.
Develop and manage comprehensive study plans, budgets, and timelines, optimizing resource utilization and maintaining a focus on efficiency.
Spearhead the resolution of intricate issues and challenges that may arise during clinical trials, employing strategic problem-solving skills and effective communication strategies.
Implement and oversee robust monitoring and validation processes throughout the study lifecycle, ensuring data integrity and maintaining high-quality standards.
Your Profile
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required Qualifications And Experience
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in clinical study management, showcasing a good grasp of the drug development process and regulatory landscape.
Proven ability in project management, handling multiple tasks concurrently, and effectively prioritizing duties.
Exceptional communication and interpersonal skills, fostering effective collaboration with diverse cross-functional teams and external partners.
Detail-oriented with an unwavering dedication to data accuracy and maintaining the highest quality standards in advanced clinical trials.
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

Work arrangement
Hybrid

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