JUMP TO CONTENT

Remote Clinical Research Associate

  1. Mexico City
JR108333
  1. Clinical Monitoring
  2. ICON Full Service & Corporate Support
  1. Mexico City
JR108333
  1. Clinical Monitoring
  2. ICON Full Service & Corporate Support

About the role

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

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 fulfill our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership, and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touchpoint. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and friendliest people in the sector, and you’ll be helping shape an industry.

What will you be doing?

The Clinical Research Associate is responsible for managing, implementing, and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs, and all applicable rules and regulations. The responsibilities of this position include but are not limited to identifying, training/initiating, and closing out study sites; conducting remote site monitoring visits and/or targeted on-site visits as needed, conducting remote site management activities, managing study sites and the required protocols, amendments and/or deviations, assuring that data is reported accurately and timelines are maintained.

The Role 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 to work on study teams that are often virtual, multi-cultural, and multi-disciplinary.

·       Serves as the primary contact for sites and investigators participating in studies.

·       Acts as a resource for internal study teams and other ICON departments
Maintains, reviews, and ensures adequacy of information and data contained in site management reports, tracking systems (CTMS or others), and other site management documents.

·       Conducts and completes remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan.

·       Participates in QA audits as needed.

·       Regularly attends and contributes to project-specific and departmental meetings
Ability and willingness to travel as needed (drive and fly) - approximately 25% of the time.

·       Reviews drug storage and drug accountability procedures (as applicable), in accordance with applicable SOPs.

·       Maintains and archives study documentation and correspondence, as needed.

·       Assists with site contracting process, as needed.

·       Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed.

·       With support, demonstrates the ability to manage site assignments and workload
Maintains Sponsor and patient confidentiality.

·       Actively participates in regular meetings with Project Managers or delegates, and/or RS 

LEAD

·       Assists in the development of site and patient enrolment strategies with the project team; works to motivate sites to meet enrolment timelines.

·       Developing knowledge of and compliance with local regulatory requirements
Compliant and current with departmental and corporate policies and procedures.

COMMUNICATION

·       Excellent written and oral skills while showing cultural awareness and understanding; strong presentation skills, and proactive interaction with the study team and site staff.

·       Demonstrates ability to provide and receive constructive feedback; appreciates team goals, respects other's point of view, and seeks advice when appropriate.


BUSINESS DEVELOPMENT

·       supports the formation of relationships with internal and external customers
May attend bid defense presentations, as needed.

·       Supports internal and external capabilities presentations.


TEAMWORK

·       Works in collaboration with internal and external colleagues to meet project objectives, timelines, and budgets.

·       Follows departmental policies and procedures.
Takes responsibility for project tasks and sees these tasks through to successful completion, with support.

·       Completes special projects and miscellaneous assignments as needed to meet project and/or department objectives.

·       Maintains professional interpersonal relationships with team, sites, and Sponsor.


PERSONAL/PROFESSIONAL DEVELOPMENT

·       Increases knowledge of therapeutic areas, GCP, and any applicable local regulatory requirements.

·       Seeks opportunities to demonstrate leadership and enhance own professional growth.

·       Actively participates in Lunch and Learns, Journal Clubs, or other internal company training sessions.

·       Keeps current on industry trends and regulations.


LEADERSHIP

·       Self-motivated, developing organizational abilities for multi-tasking.

·       Supports the LPOR management activities an initiatives.

·       Supports the development and maintenance of practice-specific process documents (e.g., SOPs and Best Practice Guidelines).

·       Supports team compliance with all relevant SOPs and Best Practice Guidelines
MANAGERIAL/ ADMINISTRATIVE.

·       Practices good time management, with support.

ADAPTABILITY

·       Demonstrates flexibility working across different time zones and working with internal and external teams.

·       Able to adapt to changes in deadlines, competing project demands, and changes in the nature of assignments, with support.


PROBLEM-SOLVING

·       Demonstrates resourcefulness and makes appropriate use of available technology and tools in seeking and implementing solutions.

·       Works well with other individuals and departments to solve problems; begins to seek solutions proactively.

 

WORK QUALITY

·       Consistently produces high-quality work, with support.

 

You will need:

·       1 year+ clinical monitoring; on-site or remotely

·       Excellent written, and oral communication in English

·       Working knowledge of MS office

Benefits of Working in ICON:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect the delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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, 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.

#LI-JH2

List #1

Day in the life

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 excell

Teaser label

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

Read more
A picture of Suzaita
Suzaita's story - an insight into working in Clinical Research

Teaser label

A Day In The Life

Content type

Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Read more
Suzaita Hipolito

by

Suzaita Hipolito

Suzaita Hipolito

by

Suzaita Hipolito

View all

Similar jobs at ICON

CRA I

Salary

Location

Hungary

Department

Clinical Monitoring

Location

Hungary

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Identify, select, initiate and closeout appropriate investigat

Reference

2025-119163

Expiry date

01/01/0001

Orsolya Berke

Author

Orsolya Berke
Read more Shortlist Save this role
CRA II

Salary

Location

Paris

Department

Clinical Monitoring

Location

Paris

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to b

Reference

2025-121493

Expiry date

01/01/0001

Katrien Dooms

Author

Katrien Dooms
Read more Shortlist Save this role
Senior CRA Home based

Salary

Location

Paris

Department

Clinical Monitoring

Location

Paris

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to b

Reference

2025-119131

Expiry date

01/01/0001

Katrien Dooms

Author

Katrien Dooms
Read more Shortlist Save this role
Clinical Research Associate Paris

Salary

Location

Paris

Department

Clinical Monitoring

Location

Paris

Remote Working

Home-Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical partners — a collaboration built on shared values of innovation, flexibility, and a joint mission to b

Reference

2025-121455

Expiry date

01/01/0001

Katrien Dooms

Author

Katrien Dooms
Read more Shortlist Save this role
Senior CRA

Salary

Location

China

Department

Clinical Monitoring

Location

China

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-120447

Expiry date

01/01/0001

Jessica Zhong

Author

Jessica Zhong
Read more Shortlist Save this role
Clinical Research Associate II

Salary

Location

Shanghai

Department

Clinical Monitoring

Location

Shanghai

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-120784

Expiry date

01/01/0001

Jessica Zhong

Author

Jessica Zhong
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above