CRA I with SSU responsibilities, sponsor dedicated

ICON; Frankfurt; Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

A leading clinical research organization in Frankfurt is seeking a Clinical Research Associate to oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data. Candidates should possess a degree in medicine or science and excellent communication skills in German and English. You'll work closely with key stakeholders and may travel to sites frequently. This role offers a competitive salary and a range of benefits focused on well-being and work-life balance.

Leistungen

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific optional benefits

Qualifikationen

• Good knowledge of ICH-GCP guidelines and ability to evaluate medical data.
• Ability to travel to sites, with a valid driver’s license.
• Strong social skills for timely query resolution.

Aufgaben

• Coordinate all activities for setting up and monitoring clinical studies.
• Prepare and review study documentation and feasibility studies as required.
• Ensure compliance with ICON’s procedures and regulatory requirements.

Kenntnisse

Collaborative relationship building

Communication in German

Communication in English

Time management

Ausbildung

University degree in medicine, science or equivalent

Jobbeschreibung

CRA I

ICON plc is a world‑leading healthcare intelligence and clinical research organisation. 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 Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analysing critical data.

What you will be doing

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor‑generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators and site staff
• Ensure patient safety by ensuring compliance with ICON’s procedures, protocols and regulatory requirements

Your profile

• University degree in medicine, science or equivalent
• Knowledge of ICH‑GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in German and English
• Good social skills enabling you to deal with queries in a timely manner
• Ability to travel to sites if needed (at least 60% of the time) and should possess a valid driver’s licence

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.

Benefits examples

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise 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 specialised 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, subsidised 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, colour, 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.

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.