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As a Clinical Research Associate (CRA) with ICON, you will be an integral part of the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. This role is categorized as home-based, allowing professionals to work remotely while actively engaging in significant contributions to clinical trials.
The responsibilities of a Clinical Research Associate are crucial for ensuring the smooth execution of clinical trials. Key responsibilities include:
Ensuring that clinical study sites are conducting their trials in compliance with the respective protocols, Standard Operating Procedures (SOPs), and applicable International Council for Harmonisation (ICH) and Good Clinical Practice (GCP) guidelines.
Conducting Investigator Profile and Clinical Site Initiation visits, as well as Clinical Site Close-Out visits for studies involving various phases and indications.
Facilitating subject enrollment at the site level through focused patient recruitment strategies and actionable plans.
Identifying site needs and issues, escalating them as necessary, and initiating corrective actions to provide solutions and facilitate the clinical trial process.
Ensuring safety reporting, including tracking and reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs).
Assisting in audit preparation, reviewing audit reports, and contributing to the resolution of any findings.
Building and maintaining professional relationships with investigators and site staff, which is essential for the success of clinical trials.
To excel in this role, candidates need to have several key qualifications and skills:
A BA/BS/BSc degree or a similar relevant qualification.
Familiarity with ICH/GCP guidelines and local codes of practice as they apply to the specific region.
Experience or training in a CRA role is preferred, which can be advantageous for understanding clinical research nuances.
Proficiency in English and German, as effective communication is essential for working with diverse teams and stakeholders.
Willingness to travel is important, as site visits are an integral part of the role.
Good working knowledge of common software applications to assist in documentation and reporting tasks.
Flexibility and teamwork skills are essential for collaborating effectively within the clinical trial framework.
Joining ICON as a Clinical Research Associate comes with various benefits aimed at ensuring a competitive and rewarding work experience. While precise salary figures are not mentioned, ICON emphasizes the importance of nurturing talent and ensuring quality among its employees. Below are some noteworthy aspects of their offer:
A competitive salary that reflects the experience and expertise brought to the role.
Various annual leave entitlements promoting work-life balance.
A range of health insurance offerings tailored to meet the needs of employees and their families.
Competitive retirement planning offerings to assist in saving and planning for future years.
Access to a Global Employee Assistance Programme providing 24-hour support through a network of over 80,000 professionals to assist employees and their families.
Life assurance and additional flexible, country-specific benefits including options like childcare vouchers, gym memberships, travel subsidies, health assessments, and more.
This emphasis on both the health and well-being of employees is integral to ICON’s approach to employee satisfaction and retention.
ICON prides itself on a diverse and inclusive workplace culture. The company recognizes that a rich diversity among its staff makes it more innovative and better equipped to serve all stakeholders. With a strong commitment to diversity, inclusion, and belonging, ICON ensures that its working environment is accessible, welcoming, and free from discrimination.
The organization's commitment to equal employment opportunities with respect to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, and veteran status emphasizes their dedication to providing a fair recruitment process for all applicants.
In conclusion, the position of Clinical Research Associate at ICON provides an exciting opportunity for individuals looking to make a significant impact in the field of clinical research. By ensuring compliance with critical guidelines and contributing to the success of clinical trials, CRAs play a vital role in advancing healthcare research. With a competitive benefits package and a commitment to inclusivity, ICON may represent a perfect fit for candidates eager to advance their careers in a supportive and dynamic environment.
This job offer was originally published on himalayas.app
This job offer summary has been generated using automated technology. While we strive for accuracy, it may not always fully capture the nuances and details of the original job posting. We recommend reviewing the complete job listing before making any decisions or applications.