Clinical Research Associate - Remote - FSP

ICON Strategic Solutions; Deutschland; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading clinical research organization is seeking a Clinical Research Associate to oversee clinical trials and ensure regulatory compliance. The ideal candidate will hold a relevant university degree, possess excellent communication skills in English, and be willing to travel 60% of the time. This role offers competitive benefits and emphasizes inclusion and support for all candidates.

Leistungen

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifikationen

• University degree in medicine, science, or equivalent.
• Excellent written and verbal communication skills in English.
• Ability to travel at least 60% of the time.

Aufgaben

• Coordinate all activities for setting up and monitoring a study.
• Run sponsor-generated queries efficiently.
• Ensure patient safety by adhering to ICON’s procedures.
• Develop strong relationships with key stakeholders.

Kenntnisse

Clinical trial coordination

Communication skills

Knowledge of ICH-GCP guidelines

Social skills

Ausbildung

University degree in medicine, science, or equivalent

Jobbeschreibung

Clinical Research Associate - Remote - FSP

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 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 analyzing 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; participating in the preparation and review of study documentation and feasibility studies for new proposals as required
• Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
• Ensuring patient safety by adhering to 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 skills in English
• Good social skills enabling you to deal with queries in a timely manner
• Ability to travel at least 60% of the time (international and domestic – fly and drive) and possession of 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.

• 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 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.