Jobsuche > Hamburg > Clinical research associate

Clinical Research Associate - sponsor dedicated

Pharmiweb
Hamburg, DE
Diese Stelle ist in deinem Land nicht verfügbar.

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 II 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 :

  • 18 months+ of monitoring experience in phase I-III trials as a CRA
  • 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 least 60% of the time (international and domestic -fly and drive) 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 : https : / / careers.iconplc.com / benefits

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.

https : / / careers.iconplc.com / reasonable-accommodations

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.

LI-RR1

Vor 8 Tagen
Ähnliche Stellenangebote
Gesponsert
Pharmiweb
Germany

As a Clinical Research Associate II 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 regula...

Gesponsert
implantcast GmbH
Buxtehude, Niedersachsen

Clinical Research Associate / CRA Medizintechnik (m/w/d). ...

Gesponsert
Pharmiweb
Germany

Minimum three years of monitoring experience, more experience preferred, with a combination of clinical research coordinator and or other relevant clinical research experience. Biorasi is looking for top performers who are as passionate about clinical research as we are – clinical trial veterans and...

Gesponsert
implantcast GmbH
Germany

Clinical Research Associate / CRA Medizintechnik (m/w/d)Der Mensch im Mittelpunkt als Patient – als. ...

Gesponsert
Pharmiweb
Germany, Homeworking

The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main point of contact for the site during a study. Coordinate timely shipment of clinical supplies and study drug to sites in collaboration with regional CRAs. CRA , Lead CRA, Project Manager and Cli...

implantcast GmbH
Hamburg, Hamburg

Clinical Research Associate / CRA Medizintechnik (m/w/d). Qualifikation als „Klinische:r Monitor:in / Clinical Research Associate“, idealerweise mit Berufserfahrung in der Betreuung von Studien mit Medizinprodukten. Koordination und Betreuung von Post-Market-Clinical-Follow-up (PMCF) -Studien und gg...

Edwards Lifesciences
Germany,

Responsible for remotely supporting field clinical research associate/ site activities to ensure the overall integrity of study implementation and adherence to study protocol at assigned clinical sites. Organizing and supervising clinical study:. Assist and conduct Clinical Monitoring activities. Se...

BeiGene
Remote, Germany
Homeoffice

The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Mentor and manage junior staff and Clinical Research Associates. Collaborates with Regional Clinical Operations Mana...

Rocket Pharmaceuticals
DE

The Senior Clinical Research Associate (Germany) will work in close collaboration with cross-functional clinical, regulatory, safety and manufacturing team members, academic partners, and external vendors. This position reports through the Clinical Operations function which is accountable for overal...

BeiGene
Remote, Germany
Homeoffice

The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Mentor and manage junior staff and Clinical Research Associates. Collaborates with Regional Clinical Operations Mana...