# Global Study Manager

**Company**: ICON Strategic Solutions
**Location**: Regional United States (PRA)
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Regional-United-States-PRA/Global-Study-Manager_JR163256?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7648e714-a66

## Description

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 at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

**Responsibilities**

Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. Key responsibilities include:

- Overseeing the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.

- Collaborating with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.

- Developing and managing study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.

- Leading the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.

- Ensuring data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.

**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.

- Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.

- Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.

- Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.

- Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials.

**Rewards & Benefits**

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

- Competitive base salary and performance-related incentives.

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

Benefits may vary depending on role and location.

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## Skills

### Required
- clinical trial management
- regulatory requirements
- project management
- communication
- data analysis

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Regional-United-States-PRA/Global-Study-Manager_JR163256?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)