Sr. Clinical Research Associate

KCR Placement; South Carolina; Sur place; USD 80 000 - 110 000; Plein temps

Avantages offerts par ce poste

Annual leave entitlements

Health insurance

Retirement planning

Global Employee Assistance Programme (

LifeWorks

Life assurance

Flexible country-specific benefits

Résumé du poste

ICON Strategic Solutions is seeking a Sr. Clinical Research Associate for the Southeast region.

You will oversee clinical trial activities, monitor sites, and ensure adherence to protocol, GCP, and regulatory requirements, while working with cross-functional teams to ensure data integrity and timely reporting. As a Senior CRA, you will guide others, provide training to site staff, and build strong relationships with site personnel, with travel around 60% to sites across the Southeast.

Qualifications

• Bachelor's degree in a relevant scientific field.
• Extensive CRA experience with regulatory knowledge.
• Proven ability to manage multiple sites and projects.
• Expertise in monitoring, data integrity, and site management.
• Strong communication and stakeholder management.
• Willingness to travel ~60%.

Responsabilités

• Monitor trial sites to ensure protocol and GCP compliance.
• Conduct site visits, assess performance, resolve issues.
• Collaborate with cross-functional teams for data accuracy.
• Provide training and guidance to site staff and CRAs.
• Build and maintain relationships with site personnel.
• Oversee monitoring tasks with focus on quality and improvement.

Connaissances

Clinical monitoring

GCP compliance

Data integrity

Site management

Cross-functional collaboration

Travel 60%

Communication

Formation

Bachelor's degree in a relevant scientific field

Outils

EDC systems

Description du poste

Sr. Clinical Research Associate - Southeast

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 CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, 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
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Willingness to travel as required (approximately 60%)

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