JUMP TO CONTENT

PRM Analyst

042410_2

About the role

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

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.
 
Overview of the role
  • Recognize, exemplify and adhere to ICON's values which centers 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.
  • Travel (approximately 10%) domestic and/or international.
  • The following responsibilities are expected to be competently and independently performed under the direction of the Manager of the Planning and Resource Management Department (PRM), applying theoretical knowledge and practical experience. The PRM Analyst I will directly contribute to the PRM department and share accountability for achieving department goals and objectives.
    • *Ensure requests requiring updates to the Resource Management database are actioned in a timely and accurate manner, according to established Service Level Agreement timelines.
    • *Support PRM Functional Leads according to established processes, including acting as backup during periods of absence and representing the PRM FL in resourcing discussions with operational leadership.
    • *Provide regular and ad hoc reports and information to operational leadership which is up to date, accurate and timely.
    • Adhere to the existing process and develop competence by performing structured work assignments.
    • Understand best practices and customer needs and apply this knowledge in the performance of the role.
    • Work under supervision initially and become independent with experience.
    • *Work as backfill for colleagues in both functional lead and PRISM roles.
    • Undertake other reasonably related duties as may be assigned from time to time.
Role Requirements
  • 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.
    • 6 months to 1 year experience in CRO will be an advantage.
    • Knowledge in Clinical Research or Planning and Resource Management is desired.
     
  • Ability to liaise successfully with senior management, clinical project teams, other ICON departments (e.g. Finance, BD and HR) and clients if required.
  • Excellent communication and interpersonal skills.
  • Competent computer skills including knowledge of Excel and Database systems.
  • 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.
Benefits of Working in ICON
 
Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes.  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.   
 
What’s Next
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to 
List #1

Day in the life

A medic holding a pen and contract
A Guide to Clinical Trial Agreements

Teaser label

Industry

Content type

Blogs

Publish date

04/07/2025

Summary

A Comprehensive Guide to Clinical Trial Agreements In the realm of clinical research, the foundation of a successful trial is built upon well-structured Clinical Trial Agreements (CTAs). These leg

Teaser label

Explore the essentials of Clinical Trial Agreements in clinical research.

Read more
Female in a lab environment
Good Clinical Practice (GCP) Fundamentals for Job Seekers

Teaser label

Industry

Content type

Blogs

Publish date

03/28/2025

Summary

 Understanding GCP Fundamentals The landscape of clinical research is continually expanding across the globe, playing a pivotal role in the development of innovative medical treatments and therapi

Teaser label

Learn the Good Clinical Practice (GCP) basics needed to excel in clinical research jobs.

Read more
Headshot of female
A Day in the Life of a Clinical Data Science Programmer

Teaser label

Our People

Content type

Blogs

Publish date

03/18/2025

Summary

    A Day in the Life of a Senior Lead Clinical Data Science Programmer In the ever-evolving world of clinical research, professionals with specialized technical skills play a crucial role in advan

Teaser label

Hear from Punitha how she advanced her clinical data science career at ICON.

Read more
View all

Similar jobs at ICON

Clinical Trial Manager

Salary

Location

Mexico

Department

Clinical Trial Management

Location

Mexico

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Manager, CTM (Clinical Trial Management) to join our diverse and dynamic team. As the Manager of CTM at ICON, you will play a pivotal role in overseeing the planning and exe

Reference

2025-118370

Expiry date

01/01/0001

Rita Villavicencio Read more Shortlist Save this role
CRA II

Salary

Location

Lima

Department

Clinical Monitoring

Location

Lima

Remote Working

Office Based

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 partnering with one of our

Reference

2025-117470

Expiry date

01/01/0001

Magda Obregon

Author

Magda Obregon
Read more Shortlist Save this role
CRA II

Salary

Location

Brazil, Sao Paulo

Department

Clinical Monitoring

Location

Sao Paulo

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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 fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR129488

Expiry date

01/01/0001

Ana Lucia

Author

Ana Lucia
Ana Lucia

Author

Ana Lucia
Read more Shortlist Save this role
Clinical Research Nurse I-PRN

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

Nurse

Job Type

Temporary Employee

Description

We are currently seeking a Clinical Research Nurse I to join our diverse and dynamic team. As a Clinical Research Nurse I at ICON, you will play a pivotal role in supporting the execution of clinical

Reference

JR127927

Expiry date

01/01/0001

Tina Geer

Author

Tina Geer
Tina Geer

Author

Tina Geer
Read more Shortlist Save this role
Clinical Research Associate 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

2025-118573

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above