JUMP TO CONTENT

Monitoring Oversite Lead - South Florida - Bilingual Spanish/English

  1. United States
2024-113089
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

As a Monitoring Oversite Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


What you will be doing:

  • Oversight Monitoring Plan Development: Develop a comprehensive oversight monitoring plan tailored to our organization's specific clinical trials and research activities.
  • Onsite and Remote Oversight Monitoring: Perform both onsite and remote oversight monitoring visits to assess protocol compliance, data accuracy, monitoring visit report review, and monitoring visit oversight.
  • Quality Control and Risk Management: Implement quality control measures and risk management strategies to proactively identify and mitigate potential risks.
  • Reporting and Recommendations: Prepare comprehensive oversight monitoring reports summarizing findings, recommendations, and corrective actions for management and regulatory agencies.
  • Provide support for local partnerships with both internal and external stakeholders to enable the country focused delivery and execution of the R&D pipeline.
  • Provide support for country level/cross study activities relating to local ‘sponsor’ relationships, oversight of CRO and country level performance, and provide local information, resource, and communication capabilities to maximize information flow in order to highlight and mitigate potential issues and efficiently resolve active issues.
  • Perform country, site, and CRO sponsor oversight activities, to ensure high quality execution of clinical trials and highlight local opportunities to drive operational excellence.
  • Maintain study information on a variety of databases and systems.
  • Work with the strategic partner CRO, and global teams to provide required information as part of defined country and site selection processes.
  • Support the maintenance of accurate contact lists, calendar information, local clinical operational intelligence and update tracking systems as needed.

You are:

  • A minimum of 6 years of experience in onsite clinical monitoring and site management across multiple therapeutic areas.
  • Excellent communication skills in English and other languages as needed per country.
  • Previous participation in site audits and regulatory inspections preferred.
  • Experience conducting co-monitoring and oversight visits with other CRAs.
  • Based in South Florida with ability to travel to LatAm 1-2 times a month 

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.

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
EPIC Interns
ICONs EPIC Internship Program

Teaser label

Career Progression

Content type

Blogs

Publish date

07/20/2023

Summary

Unlocking your Potential: The Benefits of ICON’s EPIC Internship Program  Internship programs have become a vital stepping stone for students and young professionals seeking to gain practic

Teaser label

Read more about ICON plc's EPIC (Entry-level Professionals in CRO (Contract Research Organization)) internship program.

Read more
View all

Similar jobs at ICON

CRA II

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You

Reference

2024-115131

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Colombia

Department

Clinical Monitoring

Location

Colombia

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

2024-115229

Expiry date

01/01/0001

Magda Obregon

Author

Magda Obregon
Read more Shortlist Save this role
CRA II and Senior CRA

Salary

Location

US, Portland, OR

Department

Clinical Monitoring

Location

Portland

Blue Bell

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior CRA to join our diverse and dynamic team. As a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, in

Reference

JR125304

Expiry date

01/01/0001

Meris Myers

Author

Meris Myers
Meris Myers

Author

Meris Myers
Read more Shortlist Save this role
Clinical Research Associate 2

Salary

Location

Argentina

Department

Clinical Monitoring

Location

Argentina

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

The Clinical Research Associate monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the prot

Reference

2024-114775

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Italy

Department

Clinical Monitoring

Location

Italy

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

2024-115220

Expiry date

01/01/0001

Mattia Carcangiu Read more Shortlist Save this role
Clinical Site Liaison

Salary

Location

Spain

Department

Clinical Monitoring

Location

Spain

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Site Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.The Clinical Site Liaison is a field based ex

Reference

2024-112638

Expiry date

01/01/0001

Ana Guerra Garaeta Read more Shortlist Save this role

Browse popular job categories below or search all jobs above