We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives an... read mored improve quality of life.
We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.
The Role:
Our industry leading Global Study Start Up group is growing and we are currently looking for Senior Site Activation Leads to join our evolving global team. This i
As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
The Global Clinical Study Coordinator MAO, ass
What you will be doing:
Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
Leads Local Study Team consisting of CR
What You Will Be Doing:
Designing and implementing statistical analyses for clinical trials, including the development of statistical analysis plans and interpretation of results.
Collaboratin
What you will be doing
Lead and oversee regulatory operations activities to ensure compliance with applicable regulations and guidelines.
Develop strategies for regulatory submissions and app
As a Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form develop
What you will be doing:
Developing and implementing quality assurance strategies and processes to support clinical trial activities.
Conducting quality assessments and audits to ensure complia
Responsibilities and Qualifications:
Independently conducts the following activities as assigned by Quality & Compliance (Q&C) management:
Manage Quality Issues.
Lead Quality Issue
What you will be doing:
Create or review mapping specifications for internal data and/or SDTM.
Generate or review internal data and/or SDTM datasets using internal conversion framework, utilit
As a Clinical Research Associate, your primary focus will be on the end-to-end management of clinical trials at assigned study sites. You will:
Collaborate closely with the local study team to m
What You Will Be Doing:
Develop and maintain strong relationships with clients, serving as a primary point of contact for communication and support.
Collaborate with cross-functional teams to
The role
You will lead/project manage multi-disciplinary teams on assigned projects.
Be responsible for developing, maintaining and validating standard data structure and software.
Design an
The role
You will lead/project manage multi-disciplinary teams on assigned projects.
Be responsible for developing, maintaining and validating standard data structure and software.
Design an
What You Will Be Doing:
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throug
What you will be doing
Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements.
Participate in the identif
Job Description:
Functional Knowledge:
Expert knowledge of clinical data science activities (data management/clinical systems/clinical data risk) .
Business Expertise:
Ability to u
What You Will Be Doing:
Assist senior biostatisticians in clinical study support, including study design, sample size calculations, patient randomization, data analysis, and results reporting.
The employee is expected to embrace and where possible contribute to our culture of continuous process improvement with a focus on streamlining our processes, adding value to our business and meeti
