JUMP TO CONTENT

CRA II

JR064375

About the role

This vacancy has now expired. Please click here to view live vacancies.

Are you ready to be a part of a successful study delivery team? ICON's award-winning study execution capabilities have led to the approval of 18 of the world's top 20 best-selling drugs. Make your experience count for the benefit of patients worldwide. www.iconplc.com

Responsibilities:

* Recognize, exemplify and adhere to ICON"s values which center around our commitment to People, Clients and Performance.
* As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
* *Ability and willingness to travel at least 60% of the time.(international and domestic : fly and drive)
* *Expert knowledge of ICON's SOPs/WPs, ICH, GCP and appropriate regulations.
* *Familiarity with ICON systems .
* *Maintain timelines . Ensure accuracy and completeness of data entered into ICON systems.
* Recruitment of investigators .
* *Independent and proactive coordination of all the necessary activities required to set up and monitor a study , including but not limited to the following :
Identify investigators.
Help when requested , in preparation of regulatory submissions . Design of patient information sheets and consent forms .
Ensure timely submission of protocol/consent documents for ethics/IRB approval. Pre study/placement and initiation visits. Conduct regular monitoring visits in accordance with the ICON site monitoring SOP/sponsor site monitoring SOP, as appropriate
Maintain all files and documentation pertaining to studies . Motivate investigators in order to achieve recruitment targets. Complete accurate study status reports.
Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs.
Keep the Project Manager regularly informed.
Process case record forms to the required quality standards and timelines . Deal with sponsor generated queries in a timely manner.
Ensure the satisfactory close-out of investigator sites .
Participate, if requested, in the preparation of and review of study documentation , e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report.
Participate in feasibility studies for new proposals as required. Ensure correct archiving of files on completion of a study .
Maintain patient and sponsor confidentiality .
Assume additional responsibilities as directed by the Project Manager.
- lnvestigational Products (IPs) stored and managed by the site:
* Ensure storage conditions and acceptable supplies are provided
* Ensure IPs are supplied only to eligible patients
* Ensure IP receipt, use and return are controlled and documented
* Ensure disposition of unused IP comply with regulatory requirement and are in accordance with the sponsor.
* *Act in a lead role on a study assuming additional responsibilities as detailed/documented by the Project Manager if appropriate .
* Participate in data listing reviews, as applicable .
* *Responsible for cost effectiveness
* *Participate in training and mentoring new staff up to Clinical Research Associate level as appropriate.
* Assist with marketing the company if and when appropriate . Other duties as assigned .

Benefits of Working in ICON :

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

List #1

Day in the life

Two medics at ICON clinical research clinic
The Strategic Role of Site Selection and Activation in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

07/07/2025

Summary

Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit

Teaser label

Explore the critical role of site selection and activation in clinical trials.

Read more
3 x Digital padlocks
The Role of Cybersecurity in Clinical Data Management

Teaser label

Industry

Content type

Blogs

Publish date

07/04/2025

Summary

Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio

Teaser label

Learn about the critical role cybersecurity plays in an increasingly digital research environment.

Read more
Stethoscope on paper
Specialisations in Clinical Research: Finding Your Niche

Teaser label

Industry

Content type

Blogs

Publish date

07/03/2025

Summary

Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many

Teaser label

Explore the diverse specialisations in clinical research, from clinical operations to data management, regulatory affairs, and beyond.

Read more
View all

Similar jobs at ICON

Clinical Data Reviewer

Salary

Location

United States

Department

Clinical Trial Management

Location

United States

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

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

Reference

2025-120830

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Medical Research Associate

Salary

Location

US, Salt Lake City (PRA)

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Salt Lake City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinic

Job Type

Permanent

Description

We are currently seeking a Medical Research Associate to join our diverse and dynamic team. As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volu

Reference

JR132714

Expiry date

01/01/0001

Kris Costello

Author

Kris Costello
Read more Shortlist Save this role
CRA I - Academy

Salary

Location

Argentina

Department

Clinical Monitoring

Location

Argentina

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

2025-120835

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Principal Medical Writer

Salary

Location

United States

Department

Medical Affiars & Medical Writing Roles

Location

United States

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Medical Writing

Job Type

Permanent

Description

As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-117948

Expiry date

01/01/0001

Brendan Hoey

Author

Brendan Hoey
Read more Shortlist Save this role
Senior Clinical Research Associate - Oncology Phase 1 - Midwest

Salary

Location

Chicago, United States

Department

Clinical Monitoring

Location

Chicago

United States

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

2025-120826

Expiry date

01/01/0001

Monica Hawkins Read more Shortlist Save this role
Senior Clinical Research Associate - Oncology Phase 1 - Northeast (Field Based)

Salary

Location

New York, United States

Department

Clinical Monitoring

Location

New York

United States

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

2025-120825

Expiry date

01/01/0001

Monica Hawkins Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above