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Senior Clinical Trial Transparency Associate

Senior Clinical Trial Transparency Associate

Senior Clinical Trial Transparency Associate

Senior Clinical Trial Transparency Associate

ICON

Pharmazeutische Produkte, Arzneimittel

Frankfurt am Main

  • Art der Beschäftigung: Vollzeit
  • 62.500 € – 88.000 € (von XING geschätzt)
  • Hybrid
  • Zu den Ersten gehören

Senior Clinical Trial Transparency Associate

Über diesen Job

Senior Clinical Trial Transparency Associate

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.

We are currently seeking a Senior Clinical Trial Transparency Associate to join our diverse and dynamic team. As a Senior Clinical Trial Transparency Associate at ICON Plc, you will be instrumental in ensuring the transparency and integrity of clinical trial data and results. You will contribute to the adherence to regulatory requirements, enhance the visibility of clinical trial processes, and support the organization in maintaining high standards of clinical trial reporting.

You will be responsible to plan, lead and coordinate activities for submissions documents related to redaction/anonymization activities for Health Canada PRCI and EMA Policy 0070.

What You Will Be Doing:

  • Ensuring compliance with clinical trial transparency regulations and guidelines.

  • Collaborating with cross-functional teams to implement and manage processes for the accurate reporting and disclosure of clinical trial data.

  • Overseeing the preparation and submission of clinical trial registries and results to relevant databases.

  • Providing strategic guidance on transparency practices and the interpretation of regulatory requirements.

  • Establishing and maintaining effective relationships with regulatory bodies and external stakeholders to enhance transparency efforts.

Your Profile:

  • Advanced degree in a relevant field such as life sciences, public health, or law.

  • Extensive experience in clinical trial transparency and regulatory compliance.

  • Experience with document anonymization and Health Canada PRCI and EMA Policy 0070

  • Expertise in data management and regulatory reporting, with proficiency in relevant software and systems.

  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to drive compliance and change within a complex organization.

#LI-Remote

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

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Gehalts-Prognose

Unternehmens-Details

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ICON

Pharmazeutische Produkte, Arzneimittel

Kiel, Deutschland

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