About the role
Senior Clinical Research Associate - Oncology/Myelofibrosis - US
- 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 Senior Clinical Associate at ICON, you will oversee and support the execution of clinical trials, ensuring the highest standards of quality, compliance, and efficiency.
- What You Will Do: You will lead on clinical coordination tasks requiring technical depth, with a focus on quality and continuous improvement.
- Key responsibilities include: Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
- Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
- Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
- Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
- Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.
- Your Profile: You will have a strong foundation in clinical coordination, with the experience to work independently and guide others.
- Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
- Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.
- 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
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- Are you a current ICON Employee? Please click here to apply