Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based
Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based

Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based

Vollzeit 36000 - 60000 € / Jahr (geschätzt) Kein Home Office möglich
I

Auf einen Blick

  • Aufgaben: Join us as a Clinical Research Associate, ensuring trials meet protocols and regulations.
  • Arbeitgeber: Be part of ICON, the world's largest clinical research organization focused on healthcare intelligence.
  • Mitarbeitervorteile: Enjoy competitive salary, diverse benefits, and a focus on work-life balance.
  • Warum dieser Job: Make an impact in clinical trials while building relationships with investigators and site staff.
  • Gewünschte Qualifikationen: BA/BS/BSc degree required; familiarity with ICH/GCP guidelines and experience as a CRA preferred.
  • Andere Informationen: Diversity and inclusion are core to our culture; all qualified applicants are encouraged to apply.

Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

  1. Ensures clinical study sites are conducting clinical trials in compliance with the respective protocol, SOPs and applicable ICH/GCP guidelines and regulations.
  2. Conduct Investigator Profile and Clinical Site Initiation visits as well as Clinical Site Close-Out visits for studies of all phases in a range of different indications.
  3. Facilitate subject enrolment at the site level with focused patient recruitment strategies and action plans.
  4. Identify site needs and site-related issues, escalate them and/or initiate corrective actions when necessary, providing solutions for site staff to facilitate the clinical trial process.
  5. Ensures appropriate safety reporting as well as tracking and reporting of adverse events (AEs and SAEs).
  6. Assist in preparing sites for audits, review audit reports and contributes to resolve findings.
  7. Build and maintain solid and long-term professional relationships with investigators and site staff.

You are:

  1. BA/BS/BSc degree or similar.
  2. Familiarity with ICH/GCP guidelines plus local codes of practice as applicable.
  3. Experience or Training working as a CRA.
  4. Proficiency in English and German.
  5. Willingness to travel.
  6. Good working knowledge of common software packages.
  7. Flexibility and Team skills.

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.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We’re proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.

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.

#J-18808-Ljbffr

Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based Arbeitgeber: ICON plc

At ICON, we pride ourselves on being a leading employer in the clinical research field, offering a dynamic and inclusive work culture that fosters professional growth and development. Our home-based roles in East Germany provide flexibility and a supportive environment, complemented by competitive benefits such as comprehensive health insurance, retirement planning, and a global employee assistance program. Join us to be part of a diverse team dedicated to making a meaningful impact in healthcare while enjoying a healthy work-life balance.
I

Kontaktperson:

ICON plc HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based

✨Tip Number 1

Familiarize yourself with ICH/GCP guidelines and local codes of practice. This knowledge is crucial for a Clinical Research Associate role, as it demonstrates your understanding of compliance and regulatory requirements.

✨Tip Number 2

Network with professionals in the clinical research field. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and best practices in clinical trials.

✨Tip Number 3

Highlight any previous experience or training as a CRA during interviews. Be prepared to discuss specific challenges you faced and how you overcame them, as this will showcase your problem-solving skills.

✨Tip Number 4

Demonstrate your flexibility and teamwork skills by sharing examples from past experiences. Employers value candidates who can adapt to changing situations and work collaboratively with site staff and investigators.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based

Familiarity with ICH/GCP guidelines
Clinical Trial Management
Site Monitoring
Patient Recruitment Strategies
Adverse Event Reporting
Audit Preparation and Review
Problem-Solving Skills
Communication Skills
Relationship Building
Flexibility
Team Collaboration
Proficiency in English and German
Attention to Detail
Time Management

Tipps für deine Bewerbung 🫡

Understand the Role: Make sure you fully understand the responsibilities of a Clinical Research Associate. Familiarize yourself with ICH/GCP guidelines and the specific requirements mentioned in the job description.

Tailor Your CV: Customize your CV to highlight relevant experience, especially any previous roles as a CRA or related training. Emphasize your familiarity with clinical trials and patient recruitment strategies.

Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for clinical research and your ability to build relationships with site staff and investigators. Mention your language proficiency in English and German.

Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors and that all information is clear and concise. A polished application reflects your attention to detail.

Wie du dich auf ein Vorstellungsgespräch bei ICON plc vorbereitest

✨Know Your ICH/GCP Guidelines

Make sure you are well-versed in the ICH/GCP guidelines and local codes of practice. Be prepared to discuss how you've applied these in your previous roles, as this will demonstrate your understanding of compliance in clinical trials.

✨Showcase Your Experience

Highlight your experience or training as a Clinical Research Associate. Be ready to share specific examples of how you've conducted site visits, managed investigator relationships, and resolved site-related issues.

✨Demonstrate Flexibility and Team Skills

Since the role requires flexibility and teamwork, prepare to discuss situations where you've successfully collaborated with others or adapted to changing circumstances in a clinical setting.

✨Prepare for Questions on Patient Recruitment

Be ready to talk about your strategies for facilitating subject enrollment and patient recruitment. Share any successful action plans you've implemented in past studies to show your proactive approach.

Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based
ICON plc
I
  • Clinical Research Associate (East Germany) - Sponsor Dedicated - Home Based

    Vollzeit
    36000 - 60000 € / Jahr (geschätzt)

    Bewerbungsfrist: 2027-03-18

  • I

    ICON plc

Ähnliche Positionen bei anderen Arbeitgebern
Europas größte Jobbörse für Gen-Z
discover-jobs-cta
Jetzt entdecken
>