CRA 2

Icon

·

Aug 7, 2026

Location
US, Blue Bell (ICON), United States of America
Workplace
Remote
Type
Full-time
Experience
2+ years
Education
Bachelor
Visa
Not sponsored
Source
Workday

Description

Clinical Research Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Skills

GCPClinical TrialsCompliance

Similar Jobs

30

CRA 2

Fortrea·Singapore·Onsite

2w ago

CRA 2

Fortrea·Seoul, Korea

3w ago

CRA 2

Iqvia·São Paulo, Brazil

3w ago

CRA 2

Icon·Malaysia, Kuala Lumpur·Remote

4w ago

CRA 2

Icon·Malaysia, Kuala Lumpur·Remote

4w ago

CRA 2

Icon·Blue Bell, US·Remote

1mo ago

CRA 2

Icon·Blue Bell, US·Remote

1mo ago

CRA 2

Icon·Blue Bell, US·Remote

1mo ago

CRA 2

Icon·Blue Bell, US·Remote

1mo ago

CRA 2

Iqvia·Mexico City, Mexico·Onsite

3mo ago

CRA 2

Icon·Spain, Madrid +1·Onsite

8mo ago

CRA 2 - IQVIA Biotech- Czech Republic

Iqvia·Prague, Czech Republic·Onsite

1d ago

SSU CRA 2

Icon·Mexico, Mexico City·Remote

1w ago

FSP CRA 1 & CRA 2

Iqvia·Lima, Peru·Onsite

1w ago

CRA 2, Oncology, IQVIA

Iqvia·Durham, North Carolina +3·Onsite

1w ago

Sr. CRA 2, FSP - Invitro Diagnostics - West Coast

Fortrea·Durham, US +10·Remote

3w ago

CRA 2, Oncology, IQVIA Biotech

Iqvia·Durham, North Carolina +6·Onsite

3w ago

Experienced CRA 2

Fortrea·Durham, US +22·Remote

1mo ago

CRA 2/Senior CRA 1

Iqvia·San Juan, Puerto Rico·Onsite

2mo ago

CRA 2, Early Clinical Development

Iqvia·Carlsbad, CA +2·Onsite

3mo ago

CRA 2, Single-Sponsor Dedicated

Iqvia·Amsterdam, Netherlands·Onsite

3mo ago

SR CRA 1 or CRA 2

Iqvia·Mexico City, Mexico·Onsite

4mo ago

Clinical Research Associate (CRA 2/Sr CRA 1) - Sponsor dedicated - Hungary

Iqvia·Budapest, Hungary·Onsite

5mo ago

CRA 2, Argentina, IQVIA Biotech

Iqvia·Buenos Aires, Argentina·Onsite

5mo ago

CRA 2 -Guangzhou

Syneoshealth·CHN-Client, China·Remote, Onsite

1y+ ago

FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

Fortrea·Durham, US +33·Remote

1mo ago

Consultant.e.s - Stage de fin d'études - Nantes - CYB - Quel framework et socle de sécurité à l'ère des nouvelles réglementations Européennes (NIS 2, REC, CRA, DORA) ?

Wavestone·Nantes, Pays de la Loire·Remote

1mo ago

CRA 1/2

Iqvia·Thane, Maharashtra·Onsite

1mo ago

CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada

Fortrea·Toronto, Canada +2·Remote

2mo ago

CRA SSU with at least 2 years of regulatory experience - Sponsor dedicated - Argentina Client Based

Syneoshealth·ARG-Remote, Argentina·Remote

7mo ago