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Either standalone for GCP - Trained professionals or as part of the comprehensive and advanced Clinical Research Associate (CRA) training program package, you will have the opportunity to participate in three distinct remote internships designed to provide you with real-world experience in critical therapeutic areas. These internships are carefully crafted to simulate the complexities and challenges you will encounter as a CRA, allowing you to apply theoretical knowledge in practical, hands-on scenarios and enhancing your ability to manage complex clinical trials and preparing you for advanced roles in clinical research.
Why These Internships Matter and What to Expect?
These remote internships are more than just exercises—they are a gateway to mastering the practical skills required in the clinical research industry. By participating in these internships, you will enhance your expertise in key therapeutic areas, develop critical thinking and problem-solving abilities, and gain the confidence to excel in your future career as a CRA. Here what to expect:
Mentorship and Support
Throughout each internship, you will be guided by experienced mentors who will provide feedback, answer questions, and support your learning journey.
Real-World Scenarios
You will engage in realistic case studies, virtual site visits, and hands-on assignments that mimic the daily challenges faced by CRAs in these therapeutic areas.
Comprehensive Learning
Each internship is designed to cover essential aspects of clinical trial management, including protocol adherence, data monitoring, patient safety, and regulatory compliance.
These internships are integral to your development as an advanced CRA, offering a unique opportunity to gain practical experience in managing clinical trials in oncology, cardiovascular disease, and infectious diseases. Prepare you to apply your knowledge, hone your skills, and make a meaningful impact in the field of clinical research.
These internships will be an invaluable addition to your studies and career path
Oncology Clinical Trials Internship
In the Oncology Clinical Trials Internship, you will delve into the rigorous and highly regulated field of oncology research. This internship will equip you with the skills to manage complex trials, focusing on patient safety, data integrity, and regulatory compliance. Through real-world scenarios, you will address challenges such as patient recruitment, adverse event reporting, and the meticulous oversight required in oncology studies.
Cardiovascular Disease Research Internship
The Cardiovascular Disease Research Internship offers a deep dive into the fast-paced world of cardiovascular clinical trials. You will gain hands-on experience in managing multi-site studies, with an emphasis on accurate data collection and patient monitoring. This internship will prepare you to navigate the intricacies of cardiovascular research, where precision and timely decision-making are paramount to trial success.
Infectious Diseases Clinical Trials Internship
In the Infectious Diseases Clinical Trials Internship, you will be immersed in the dynamic and ever-evolving field of infectious disease research. This internship focuses on the rapid and flexible management of clinical trials, with a particular emphasis on vaccine development, antimicrobial resistance, and outbreak response. You will engage in scenarios that require quick thinking and adaptability, reflecting the real-world challenges of infectious disease trials.
Objective
Equip students with in-depth knowledge and hands-on experience in the complexities of managing oncology clinical trials, focusing on the challenges of patient recruitment, adverse event reporting, and protocol adherence in a highly regulated environment
Key Activities
Monitor remote clinical sites involved in vaccine trials or treatment studies for emerging infectious diseases, ensuring timely and accurate data entry.
Conduct remote source data verification (SDV) to ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.
Participate in virtual site visits and audits, addressing specific oncology trial challenges such as patient safety, informed consent, and ethical considerations.
Objective
Provide students with practical experience in conducting cardiovascular clinical trials, emphasizing the importance of accurate data collection, patient monitoring, and managing multi-site studies in a fast-paced therapeutic area.
Key Activities
Perform remote monitoring of clinical data related to interventions like stent placements, cardiac monitoring, and lifestyle management programs.
Engage in remote risk-based monitoring, focusing on high-risk sites and critical data points related to cardiovascular outcomes.
Collaborate in virtual team meetings to discuss protocol deviations, adverse events, and data trends, with a focus on improving trial efficiency and patient outcomes
Objective
Immerse students in the dynamic field of infectious disease research, where they will gain hands-on experience in the rapid and flexible management of trials, with a focus on vaccine development, antimicrobial resistance, and outbreak response.
Key Activities
Monitor remote clinical sites involved in vaccine trials or treatment studies for emerging infectious diseases, ensuring timely and accurate data entry.
Conduct remote audits of patient records and laboratory results, focusing on the compliance of sites with protocol and regulatory standards.
Participate in remote cross-functional meetings, contributing to discussions on trial adaptations in response to emerging data, site challenges, and evolving public health guidelines.
