Clinical Study Manager

Regulatory Jobs; Center Square (PA); Presencial; USD 90.000 - 130.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Descripción de la vacante

ICON Strategic Solutions is seeking a Clinical Study Manager to oversee the design, execution and analysis of clinical trials. You will coordinate cross-functional teams, ensure regulatory compliance, and drive study timelines to deliver high-quality data that supports patient outcomes.

The role emphasizes strong project management, collaboration with investigators and vendors, and meticulous attention to data integrity across the study lifecycle.

Formación

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Proven experience in clinical study management with understanding of drug development and regulatory requirements.
• Excellent project management skills with ability to handle multiple tasks and priorities.
• Strong communication and interpersonal skills for cross-functional collaboration with investigators, vendors and partners.
• Detail-oriented with focus on data accuracy and high-quality trial standards.

Responsabilidades

• Oversee planning, execution, and monitoring of clinical trials to ensure regulatory compliance and timelines.
• Collaborate with investigators, vendors, and internal stakeholders to drive study implementations.
• Develop and manage study budgets, resources, and timelines to optimize study plans.
• Lead resolution of issues during trials with effective problem-solving and communication.
• Ensure data integrity and quality through monitoring and validation throughout the study lifecycle.

Conocimientos

Project management

Cross-functional collaboration

Data integrity

Communication

Clinical trial management

Educación

Bachelor's degree in science

Descripción del empleo

Clinical Study Manager

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.

What You Will Do:

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

• Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
• Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.
• Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.
• Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.
• Ensure 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.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.