Senior CRA

PharmaJobber; Deutschland; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading healthcare intelligence firm in Germany is seeking a Clinical Research Associate to monitor and manage clinical trials. Responsibilities include preparing documentation, ensuring regulatory compliance, and conducting site visits. The ideal candidate will have at least 4 years of clinical trial experience and excellent communication skills in both English and German. This role offers a competitive salary and various benefits aimed at promoting well-being and work-life balance.

Leistungen

Various annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifikationen

• 4 years of experience in clinical trials.
• Previous monitoring experience in medium-sized studies.
• Availability to travel up to 50% of the time.

Aufgaben

• Set up and monitor studies, complete reports, and maintain documentation.
• Submit protocol and consent documents for ethics approval.
• Prepare regulatory submissions and review study documentation.

Kenntnisse

Clinical trial experience

Excellent communication in English and German

Knowledge of ICH-GCP guidelines

Ability to work to tight deadlines

Proactive work approach

Ausbildung

Degree in medicine, science, or equivalent

Jobbeschreibung

Overview

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.

As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people’s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.

What you will be doing

• Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
• Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
• Balancing sponsor generated queries
• Taking responsibility for study cost efficiency
• Preparation and review of study documentation and feasibility studies for new proposals
• Potential to assist in training and mentoring fellow CRAs

You are

• 4 years of experience in clinical trials
• Degree in medicine, science, or equivalent
• Previous monitoring experience in medium-sized studies, including study start-up and close-out
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Excellent written and verbal communication in both English and German
• Ability to work to tight deadlines
• Availability to travel up to 50% of the time (international and domestic) and should possess a valid driving license

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 maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, 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 website to read more about the benefits of working at ICON: careers iconplc dot com benefits

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.

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.