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Senior Clinical Trial Manager Womens Health

At ICON, we are lookingfor specialist experience in Women"s Health clinical studies?The role

Site Engagement Liaison

Site Engagement LiaisonUS - Homebased Position ICON, a leading provider in clinical trial services, management and delivery, is looking for an experienced patient recruitment professionals to join our dynamic team. The Site Engagement Lia

Director Study Start Up

Are you proven leader in project management with a track record in managing large portfolios of clinical studies that improve lives every day? About the Director, Study Start Up at ICON:The role is to support Study Start activities.  You

Director Feasibility Strategy

Are you proven leader in project management with a track record inmanaging large portfolios of clinical studies that improve lives every day?

Clinical Trial Manager

Clinical Trial Manager - Internal Medicine Based anywhere in US (homebased)  The role As a Clinical Trial Manager you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our

Sr Tech Reporting Specialist - Farmingdale NY

Laboratory Senior Technical Reporting SpecialistLocation: Farmingdale, NY 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, bio

Project Leader - Market Access and Reimbursement - South San Francisco CA

 Project Leader - Market Access & ReimbursementSouth San Francisco, CA (Office-Based) The Market Access & Reimbursement (MAR) group at ICON plc is a multidisciplinary team of experts that focuses exclusively on market access an

CTA

Clinical Trial Assistant (CTA)Location: Warsaw, Poland At ICON, it’s our people that set us apart. As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it.

CTA

Clinical Trial Assistant (CTA)Location: Riga, Latvia At ICON, it’s our people that set us apart. As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. W

Senior CRA

• 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 I expected to embrace and contribute to our culture of process improvement with a focus on

Senior CRA

Per Job Code 50405 - SCRA: • 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 I expected to embrace and contribute to our culture of process

Sydney

Senior CRA

• 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 I expected to embrace and contribute to our culture of process improvement with a focus on

Sydney

Project Leader I

Are you interested in managing the day-to-day activities of pharmaceutical studies within a bioanalytical laboratory?

Project Leader - Market Access and Reimbursement - San Francisco CA

Project Leader - Market Access & ReimbursementSan Francisco, CA (Office-Based) The Market Access & Reimbursement (MAR) group at ICON plc is a multidisciplinary team of experts that focuses exclusively on market access and reimbursem

Clinical Trial Manager

Position Name : Clinical Trial ManagerLocation : Tokyo or Osaka, JapanThis is an exciting opportunity to join ICON as Clinical Trial Manager. Our Clinical Trial Managers act as the Functional Lead from Clinical Operations with responsibility f

Clinical Trial Manager

Position Name : Clinical Trial ManagerLocation : Tokyo or Osaka, JapanThis is an exciting opportunity to join ICON as Clinical Trial Manager. Our Clinical Trial Managers act as the Functional Lead from Clinical Operations with responsibility f

Proj Manager Data Management

Project Manager, Data Management 

CDL

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 Clinical Data Lead plays a key ro

CTA

TBC

Study Start Up Associate Contracts and Budgets

Study Start Up Associate (Contracts & Budgets)

Study Start Up Associate Contracts and Budgets

Study Start Up Associate (Contracts & Budgets)

Talent Acquisition Specialist

CONTRACT TALENT ACQUISITION SPECIALIST Are you a seasoned talent acquisition professional who is interested to join a global top rated contract research organization? At ICON, as part of our TA team, you will join our HR Community and partne

CTA Supervisor

 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. Our CTA Supervisor will play a

Medical Writer I - UK or US

Medical Writer I - UK or USThis is a rare opportunity to join our friendly global Medical Writing team which sits within ICON’s Clinical Research Services group. Our remit is to produce high quality documents supporting clinical studies and regulat

Principal Health Economics

Senior Principal, Health Economics 

Clinical Trial Manager

Position Name : Clinical Trial ManagerLocation : Tokyo or Osaka, JapanThis is an exciting opportunity to join ICON as Clinical Trial Manager. Our Clinical Trial Managers act as the Functional Lead from Clinical Operations with responsibility f

Clinical Trial Manager

Position Name : Clinical Trial ManagerLocation : Tokyo or Osaka, JapanThis is an exciting opportunity to join ICON as Clinical Trial Manager. Our Clinical Trial Managers act as the Functional Lead from Clinical Operations with responsibility f

Centralized Clinical Trial Manager

“At ICON, it"s our People that set us Apart”Are you passionate about improving the quality of human life? If so, we invite you to join us in building a healthier world tomorrow. Why ICON?ICON is a global provider of outsourced development serv

Analytics Development Lead

Are you looking for an exciting career development opportunity? Do you want to learn more about clinical data analytics and risk-based monitoring?Risk-based monitoring (RBM) is central to the way clinical trials are conducted, and ICON uses a varie

Internal Auditor

Internal Auditor Location: Dublin Do you have experience within Internal Audit and are looking to join a leading Irish Plc? Do you enjoy collaborating with cross functional teams internationally? ICON plc, a leading Contr

Regional Manager Facilities and Administration - London

Facilities and Administration - Regional Manager (EMEA & APAC) Location: London ICON plc, a leading Clinical Research Organisation employing 14,000 people across 80 offices in 38 countries, seeks a highly motivated Manager to join

Clinical Data Programming Lead

Clinical Data Programming Lead

Study Manager

We are looking for passionate, resilient, and supporting individuals to join our growing team. As a Study Manager, you will play an integral role within a hardworking team rated as one of the best places to work by Forbes magazine for three years i

Proj Manager Data Management

Project Manager, Data Management 

Client Services Assoc II PCS

Client Services Associate II Mapi Research Trust is a non-profit organization dedicated to improving patients’ quality of life by facilitating access to Patient-Centered Outcome (PCO) information. Mapi Research Trust promotes scientific a

Research Assistant - Per Diem

We are looking for Research Assistants to join our winning team rated by Forbes as one of America’s best employers for two years in a row! Do you have experience ensuring execution of all clinical study protocol activities within Good Clinical

Research Assistant - Must Be Licensed LPN LVN RN - Full Time Monday-Friday 1p-9 30p

We are looking for Research Assistants to join our winning team rated by Forbes as one of America’s best employers for three years in a row!Do you have experience ensuring execution of all clinical study protocol activities within Good Clinical Pra

Research Assistant - Must Be Licensed LVN RN LPN - Full Time Overnight Thursday 7p-7a FridayandSaturday 7p-9a

We are looking for Research Assistants to join our winning team rated by Forbes as one of America’s best employers for three years in a row!Do you have experience ensuring execution of all clinical study protocol activities within Good Clinical Pra

Clinical Trial Manager Oncology - Homebased

Clinical Trial Manager - Oncology  

Project Manager Interactive Response Technology IRT

Are you a motivated individual with an“own-it” mentality capable of driving projects through their entirety? Do youhave a deep understanding of IRT and/or IT System Development Life Cycle (SDLC)processes? Want to be a part of an organization tha

Study Start Up Associate II

ICON is hiring for Study startup group “At ICON, it"s our People that set us Apart”

Study Startup Associate II

ICON is hiring for Study startup group “At ICON, it"s our People that set us Apart”

Financial Analyst II

Financial Analyst II – ICON’s Functional Services Location: Dublin Are you looking for a dynamic and meaningful Financial Analyst role in the finance function of an Irish headquartered Plc? Are you a qualified accountant with 2-

Project Manager Cardiovascular - Homebased

Doyou think you have what it takes to be a part of a successful study deliveryteam? ICON’s award-winning study execution capabilities have led to theapproval of 18 of the world’s top 20 best-selling drugs. Make your experiencecount for the bene

Medical Writing Manager

Medical Writing ManagerUK or US - home based or office basedThis is a rare opportunity to join our friendly global Medical Writing team which sits within ICON’s Clinical Research Services group. Our remit is to produce high quality clinical/regulat

Principal Medical Writer

Are you an ambitious experienced Medical Writer? Do you have a reputation for being a motivational leader? If so we would love to hear from you.As an ambassador both internally and externally for ICON’s Medical Writing department, you will be respo

Senior Medical Writer - Imaging

Medical Writer - ImagingThis is a rare opportunity to join our friendly global Medical Writing team which sits within ICON’s Clinical Research Services group. Our remit is to produce high quality documents supporting clinical studies and regulatory

QC Analyst - Medical Writing

QC Analyst – Medical Writing Location: US/UK home based or office basedThe roleQuality control of regulatory documents.Provide additional writing and/or editing services, as required.Liaise with internal groups, i.e., Biostatistics, Data Management


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