SMA II

ICON Strategic Solutions; France; Sur place; EUR 36 000 - 52 000; Plein temps

Avantages offerts par ce poste

Health insurance

Retirement planning

Global EAP LifeWorks

Flexible benefits

Travel opportunities

Résumé du poste

ICON plc is seeking an experienced Clinical Trial Assistant with site coordination skills to support CRAs in preparing site initiation files. You will contribute to clinical research activities, coordinate monitoring at sites, and assist in regulatory document preparation while collaborating with cross-functional teams.

You will track site performance, analyze data, and provide reports to enhance trial management. Travel up to 25% may be required as part of the role.

Qualifications

• Bachelor's degree in life sciences, healthcare, or clinical research.
• Experience in clinical research, site management, or monitoring.
• Strong organizational and project management skills.
• Excellent analytical abilities and high attention to detail.
• Excellent communication and relationship-building with site staff.

Responsabilités

• Coordinate monitoring activities at clinical trial sites and ensure protocol adherence.
• Assist in preparing and reviewing regulatory documents for compliance with GCP.
• Collaborate with cross-functional teams to support trial sites throughout the study lifecycle.
• Track site performance, analyze data, and provide reports to improve site management.
• Mentor junior staff and support ongoing training initiatives.

Connaissances

Clinical trial coordination

Regulatory documentation

GCP knowledge

Communication skills

Travel readiness

Formation

Bachelor's degree in life sciences or clinical research

Outils

EDC systems

Regulatory portals

Description du poste

Great role for an experienced CTA with clinical study coordination skills to support CRAs with preparing site initiation files

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What You Will Do

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively.

Key Responsibilities Include

• Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.
• Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations.
• Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle.
• Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency.
• Participating in training initiatives and mentoring junior staff to support their development in clinical trial management.

Your Profile

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required Qualifications And Experience

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
• Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines.
• Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines.
• Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards.
• Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams.
• Willingness to travel as required (approximately 25%)

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