Data Scientist  Location: Bangalore, India [Officebased - hybrid model] As a Data Scientist, you will be fully dedicated to one of our global pharmaceutical partners—a company renowned for performance, innovation, and quality. This role offers the best of both worlds: the stability and support of a top CRO and the agility of a pharma environment that values innovation and...

As a Data Scientist, you will be dedicated to one of our global pharmaceutical clients, a company that values performance, recognizes merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.   The Data Scientist is responsible for contributing to the development of the strategy for Analytics, Reporting and Metrics building in line with overall Business Information Services strategy leveraging

As a Senior TMF Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.   You will be joining one of our global pharmaceutical clients; a prestigious organization, specializing in a  niche  rare disease,  complemented  by a  pipeline in  other therapeutic areas, including oncology. A company that is driving the next generation of patient treatment, where individuals are empowered to...

As a CRA II based in Culiacan  you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently but always as part of the client and ICON plc team.

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.

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

The Clinical Trials Assistant (CTA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives

Title: (Senior) Manager, Clinical Operations Working location: ICON office based in Taiwan   As a (Senior) Manager, Clinical Operations you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Location: Delhi   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 continuous improvement. This...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.   Job Title: Group Lead Clinical Data Science Location : Bangalore/ Chennai/ Trivandrum

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

We are constantly looking for motivated, reliable and dedicated CTMs who can demonstrate a first similar experience as a Clinical Trial Manager, Local Trial Manager or Study Manager within the pharmaceutical industry or a CRO.   As a Clinical Trial Manager you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation,...

As a Clinical Trial Manager you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions.

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.

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

A Senior Medical Writer is a professional who contributes to drug and device development through independently writing, editing, and compiling scientific documents related to clinical trials (narratives and summarize data from biostatical tables/listings). This role may assist with resource management A Senior Medical Writer may reside in either Early Phase or Medical Writing Publishing or MediMedia.

The Sr. Study Start Up Associate fulfills the role of Local Regulatory Affairs Lead (LRAL) and is responsible for preparing, submitting and following up on initial and amended Regulatory Agency (RA), Central Independent Ethics Committee (IEC), and any other central submissions required in the country(s) they are responsible for, within contracted timelines and budget, in accordance with local regulatory requirements and sound scientific/technical principles, including the creation and modification of documentation required for approval.

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

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 success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.  

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.    You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to...