As a Manager, Site Engagement Liaison, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   The Site Engagement Liaison Manager is a field based expert who supports the conduct and the patient recruitment of the client global clinical trials at investigative sites, through local and relational support.

As a IRT Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.  

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

As a Digital Health Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

As a Sponsor Dedicated CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

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

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

*Location: Mumbai/Pune*   As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.

As a Clinical Data Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Location : Bangalore/Chennai/Trivandrum[OFFICE-BASED on Hybrid Model]  Immediate joiners only

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare Sweden and Norway.

ICON PLC is seeking a highly skilled and experienced Clinical Data Science Programmer to join our team. The ideal candidate will have over 4 years of experience working within Data Warehouse platforms in a regulated industry, specifically within a clinical trial environment (IDAR). This role demands a deep understanding of data visualization tools, scripting languages, and SDTM data structures, along with the ability to work independently on complex assignments.

Contract Analyst is responsible for direct site-facing contract and budget negotiations throught contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or pCRO and collaborating with other lines to plan site contracting timelines though start-up.

As a Clinical Document Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   This role focuses on quality control of regulatory submission documents and is dedicated to global pharma company. This role involves tasks related to formatting and document/project management of regulatory documents.  

Home-based, Location: Delhi and Chennai    As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will have an opportunity to work in a solid partnership and an environment driven by innovation and...

As a Sr. Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Physician providing medical expertise to ensure timely planning, designing, conduct, monitoring, and reporting of clinical trials.

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

As a Principal Clinical Data Science Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. In this role you will be responsible for overseeing all aspects of clinical data management for assigned trials, ensuring data integrity, regulatory compliance, and timely deliverables. The role includes cross-teams collaboration, internal teams, and vendors. The Principal Clinical Data Science Lead ensures the accuracy and completeness of clinical data for regulatory submissions and supports process improvements.

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, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our...

Senior Contract Analyst Location: Home-Based, Australia   As a Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   Within this program you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client,