Clinical Research Associate II
WFA Digital Insight
The demand for clinical research professionals with expertise in remote work and digital skills has grown significantly, with the global clinical trials market expected to reach $68.9 billion by 2026. As a Clinical Research Associate II at ICON, you'll be at the forefront of bringing new medicines and treatments to patients faster. With a strong background in scientific or healthcare-related fields and experience in clinical trial monitoring, you'll be well-positioned to succeed in this role. According to recent statistics, companies like ICON are leading the charge in innovative treatments and therapies, making this an exciting time to join the industry. Before applying, candidates should be aware of the importance of attention to detail, strong organizational skills, and the ability to work collaboratively in a fast-paced environment.
Job Description
About the Role
The Clinical Research Associate II role at ICON is a remote position based in Buenos Aires, Argentina, that plays a critical part in the company's mission to bring new medicines and treatments to patients faster. As a values-driven organization, integrity, collaboration, agility, and inclusion are at the heart of how ICON works and interacts with customers, patients, and suppliers. In this role, you will design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.As a Clinical Research Associate II, you will be responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. You will also ensure protocol compliance, data integrity, and patient safety throughout the trial process. Your expertise in clinical trial processes, regulations, and ICH-GCP guidelines will be essential in this role.
What You Will Do
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports
- Design and analyze clinical trials, interpreting complex medical data
- Develop and implement effective strategies to manage and mitigate risks associated with clinical trials
- Collaborate with cross-functional teams, including data management, biostatistics, and medical writing
- Develop and maintain relationships with investigators, site staff, and other stakeholders
- Stay up-to-date with industry developments, regulations, and best practices in clinical research
- Participate in training and professional development opportunities to maintain and enhance skills and knowledge
What We Are Looking For
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- Mandatory advanced English
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Willingness to travel as required (approximately 60%)
- Experience with electronic data capture systems and clinical trial management systems
- Knowledge of regulatory requirements and guidelines for clinical trials
Nice to Have
- Experience with clinical trial software and systems
- Certification in clinical research or a related field
- Experience working in a remote or distributed team environment
Benefits and Perks
- Competitive base salary and performance-related incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programs and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Remote work stipend and equipment allowance
- Flexible working hours and work-from-home options
How to Stand Out
- Make sure to highlight your experience with clinical trial software and systems, such as electronic data capture systems and clinical trial management systems.
- Develop a strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP guidelines.
- Create a portfolio that showcases your experience in clinical research, including any publications, presentations, or awards.
- Be prepared to discuss your experience with data analysis and interpretation, as well as your ability to work collaboratively with cross-functional teams.
- Research the company culture and values, and be prepared to discuss how your own values and work style align with those of ICON.
- Consider obtaining certification in clinical research or a related field to demonstrate your expertise and commitment to the field.
- Prepare to discuss your experience with remote work and distributed teams, and how you stay connected and productive in a remote environment.
This is a remote position listed on WFA Digital, the platform for professionals who work from anywhere. Browse more remote jobs across all categories.