JUMP TO CONTENT

CRA - Sponsor Dedicated

  1. Austria
2024-108457
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

This vacancy has now expired. Please see similar roles below...

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.

 

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. Drive and execute monitoring plans, ensure site GCP compliance, write trip reports, resolve issues and facilitate open issue resolution, work on recruitment strategies, and monitor safety at the site.  The CRA  will conduct site qualification visits as assigned, site initiation visits and site training, routine monitoring visits, and site close-out visits. Perform investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs).


  • What you will be doing, Including but not limited to:

    • Adhere with corporate internal polices and requirements, including submission of timesheets and expense reports in a timely manner
    • Knowledge of applicable SOPs, guidelines and study procedures
    • Conduct study start-up activities related to in-house monitoring activities
    • Assist with protocol and CRF review
    • Complete study feasibility and site selection activities
    • Conduct telephone screening interviews, administer site questionnaires, collect and review regulatory documents, assist with investigator grants negotiation
    • Assist with investigator meeting activities including organization, preparation, and attendance
    • Provide status of site activity to Project Manager
    • Perform site management activities including but not limited to site qualification visit, site initiation visits, site training, site routine monitoring visit, and site close out visits
    • Establish and maintain good rapport with study sites;a.maintain frequent telephone communication with sites, providing guidance to study coordinators and investigators as necessary and in agreement per monitoring plan
    • Write study visit reports and follow up letters within the timeline established by the applicable SOPs and guidelines
    • Coordinate timely shipment of clinical supplies and study drug to sites in collaboration with regional CRAs
    • Maintain adequate site tracking records
    • Follow up of drug safety issues and safety reports in timely manner
    • Communicate site study issues, concerns, and progress to Sr.CRA , Lead CRA, Project Manager and Clinical Operations Manager accordingly
    • Assist with the implementation of corrective actions when appropriate
    • Conduct in-house review of Case Report Forms
    • Assist with data query resolution
    • Perform telephone monitoring activities in order to obtain study status information
    • Prepare/review all patient tracking records
    • Input and maintain study information in tracking systems
    • Provide information concerning subject status for financial reimbursement to sites
    • Conduct and assist with administrative activities as a member of the project team;attend staff/project team meetings as required, document all investigator information and study contacts, assist with execution of investigator agreements and grant negotiations, prepare reports as defined by SOPs
    • Ensure adherence to cost effective travel.

 

 

You are:

  • First Experience as CRA, including conducting monitoring visits for clinical trials, from either a pharmaceutical company or a CRO environment.
  • A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
  • You will be educated to degree level in a life science discipline or be a licensed healthcare professional.
  • Fluency in German and English is essential
  • Scientific degree (BSc, MSc or PhD), have equivalent experience or be a licensed healthcare professiona


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

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.

List #1

Day in the life

Man with headphones on looking at a laptop
Tips to make a lasting impression in a video interview

Teaser label

Career Progression

Content type

Blogs

Publish date

05/10/2024

Summary

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv

Teaser label

Ace your virtual job interview with these proven video interview tips.

Read more
A picture of Debora Oh
How to excel as a CRA in a Clinical Research Organisation

Teaser label

Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Teaser label

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Read more
A picture of Yemi Moses
Progressing as a CRA with ICON

Teaser label

Our People

Content type

Blogs

Publish date

05/23/2023

Summary

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

Teaser label

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

Read more
View all

Who we are

Press play to find out more

Similar jobs at ICON

Senior CRA

Salary

Location

Argentina

Department

Clinical Monitoring

Location

Argentina

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.  A CRA is a professional who cont

Reference

2023-103904

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Clinical Research Associate II

Salary

Location

France

Department

Clinical Monitoring

Location

France

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

2023-106829

Expiry date

01/01/0001

Dominique Carilien Read more Shortlist Save this role
Clinical Research Associate II - GTA Toronto

Salary

Location

Toronto

Department

Clinical Monitoring

Location

Toronto

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

2024-111010

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
CRA I

Salary

Location

Argentina, Buenos Aires

Department

Clinical Monitoring

Real World Solutions

Location

Buenos Aires

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own

Reference

JR120131

Expiry date

01/01/0001

Sarah Wood

Author

Sarah Wood
Sarah Wood

Author

Sarah Wood
Read more Shortlist Save this role
CRA I - Sponsor Dedicated

Salary

Location

Regional Greece (PRA)

Location

Greece

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR121069

Expiry date

01/01/0001

Denitsa Krasteva Read more Shortlist Save this role
CRA II - Bulgaria

Salary

Location

Bulgaria, Sofia

Department

Clinical Monitoring

Real World Solutions

Location

Sofia

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own

Reference

JR121043

Expiry date

01/01/0001

Denitsa Krasteva Read more Shortlist Save this role

Browse popular job categories below or search all jobs above