JUMP TO CONTENT

Senior Project Analyst

054492_2

About the role

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

Senior Project Analyst

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The Senior Project Analyst supports the assigned C&SR department or functional team through the independent management of assigned projects and tasks. The Senior Project Analyst works closely with other members of the project team, client, clinical/scientific teams, and internal and external clients and vendors for successful project execution. The Senior Project Analyst may also support the training of more junior staff.

 General

·         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 recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

·         Travel (approximately 10%) domestic and/or international

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Experience

•US/LATAM/CAN:  A minimum of 2 years work experience in a similar role.

•EU/APAC:  Prior relevant industry experience.

Skills

•Fluency in English both orally and in writing, with excellent communication skills.

•Strong organization and multitasking skills.

•Ability to work in a fast paced project environment.

•Strong team player in a multi-cultural environment.

•Strong problem-solving skills.

•Demonstrates attention to detail

•Ability to take action to achieve goals and targets.

•Ability to learn new tools, technologies and strategies related to the department’s service area.

•Ability to clearly present instructions, negotiate pricing and address issues with suppliers and internal and external stakeholders.

•Demonstrated ability to work well in a team environment of peers and leaders, and other colleagues across offices and departments.

•Expert proficiency in MS Word, PowerPoint and Excel.

•Ability to deliver on time sensitive demands and ongoing commitments with minimal supervision.

•Able to effectively communicate information and discuss complex issue in meetings and in written communication.

•Due to the nature of this position it may be required for the employee to travel.  Therefore dependent on the employee’s location, the employee may be required to possess a valid Driver’s license

 

Knowledge Requirements

•Strong knowledge in applicable field of health economics, outcomes research, clinical translation, eCOA technology, and/or clinical research.

               Knowledge in project management methodology.

•Strong understanding of the methods and practices being utilized in the department and in context of clients’ needs

 

Additional Language Services Department Requirements:

•Proficiency in CAT tools and Translation Management Systems required.

•Proficiency in non-English Language (preferred).

 

What’s Next?

 

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

 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

Nurse and patient
Patient Centricity in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

05/07/2025

Summary

Patient Centricity in Clinical Research: What it is and Why it Matters In the past, clinical research was designed around the needs of sponsors, researchers, and regulatory bodies. Patients were of

Teaser label

Discover how patient centricity is reshaping clinical research by placing participants at the heart of study design and execution.

Read more
Liquid capsules
Navigating Regulatory Landscapes - FDA, EMA, & MHRA

Teaser label

Industry

Content type

Blogs

Publish date

05/05/2025

Summary

Navigating Regulatory Landscapes:     Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro

Teaser label

Compare FDA, EMA, and MHRA regulatory frameworks for clinical trials, and why this knowledge matters.

Read more
Liquid drug vials in palm of hand
Understanding INDs and NDAs in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c

Teaser label

Discover the difference between IND & NDA applications, and the steps from drug development to regulatory approval.

Read more
View all

Similar jobs at ICON

Site Care Partner

Salary

Location

Taipei

Department

Clinical Trial Management

Location

Taipei

Remote Working

Office Based

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

Jot Title: Site Care PartnerWorking location: client office based (Flexible WFH)Sponsor: Top 10 Global pharma ICON plc is a world-leading healthcare intelligence and clinical research organization. We

Reference

2025-119251

Expiry date

01/01/0001

Sandy Tang

Author

Sandy Tang
Sandy Tang

Author

Sandy Tang
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Beijing

Department

Clinical Monitoring

Location

Beijing

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. 

Reference

2025-117161

Expiry date

01/01/0001

Sunshine Yang

Author

Sunshine Yang
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Guangzhou

Department

Clinical Monitoring

Location

Guangzhou

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.

Reference

2025-117160

Expiry date

01/01/0001

Jessica Zhong

Author

Jessica Zhong
Read more Shortlist Save this role
Senior Feasibility Specialist

Salary

Location

Mexico

Department

Regulatory, Drug Safety/ Quality Assurance & Other roles

Location

Mexico

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Other

Job Type

Permanent

Description

As a Senior Feasibility Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2025-119242

Expiry date

01/01/0001

Rita Villavicencio Read more Shortlist Save this role
Senior Clinical Study Lead

Salary

Location

United States

Department

Clinical Trial Management

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

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

Reference

2025-119201

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Study Start Up CRA

Salary

Location

Canada

Department

Clinical Monitoring

Location

Canada

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

The Study Start Up CRA is accountable for site selections as well as study specific start up activities and deliverables of assigned sites for Phase I-IV trials in the country in accordance with monit

Reference

2025-119257

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above