Clinical Research Coordinator - Temporary

As a Clinical Research Coordinator at the Scheie Eye Institute, your main responsibilities include overseeing clinical trial protocols, coordinating patient recruitment and screening, managing data collection and ensuring compliance with regulatory requirements. You will collaborate with researchers and healthcare professionals to facilitate the trials' day-to-day operations, ensuring that all documentation is accurate and up to date.

To apply for the Clinical Research Coordinator - Temporary position at the Scheie Eye Institute, candidates typically need a bachelor’s degree in a relevant field, such as life sciences or health care. Previous experience in clinical research or coordinative roles can be highly beneficial. Strong communication skills and an ability to effectively manage multiple tasks in a fast-paced environment are also essential.

The salary for the Clinical Research Coordinator - Temporary role at the Scheie Eye Institute ranges from $7.25 to $22.36 per hour. The exact pay rate will depend on your qualifications, experience, and skills as they relate to the position and the current market data.

At the University of Pennsylvania, you can expect a collaborative and engaging work environment as a Clinical Research Coordinator. The Scheie Eye Institute fosters a culture of support, innovation, and respect, providing you with the opportunity to work alongside dedicated professionals who are passionate about advancing medical research. The institute is located within the vibrant city of Philadelphia, making it a great place to learn and grow both personally and professionally.

Yes, temporary Clinical Research Coordinators at the Scheie Eye Institute are eligible for various benefits, including comprehensive medical and dental insurance. The University of Pennsylvania also offers retirement plans and access to other resources to support your well-being and career.

Be prepared to discuss your previous roles and how they relate to clinical research coordination. Highlight specific projects where you managed timelines, recruited participants, and maintained documentation. Give examples that demonstrate your organizational skills and attention to detail.

Compliance is critical in clinical research. Explain your understanding of regulations such as IRB approvals, informed consent processes, and data protection measures. Share strategies you’ve used in the past to ensure compliance, such as regular training and thorough audits.

Address this question by discussing a specific challenge you've faced in recruitment. Describe how you identified the problem and the solutions you implemented, including outreach strategies, imploring community resources, or enhancing patient engagement.

Share your experiences interacting with patients, emphasizing empathy and communication. Discuss how you built rapport, explained complex processes simply, and ensured that participants felt informed and comfortable throughout their involvement in the study.

Mention specific data management tools you have experience with, such as clinical trial management systems (CTMS), electronic data capture (EDC) software, or statistical analysis programs. Highlight how these tools have streamlined your workflow or improved data accuracy.

Demonstrate your organizational skills by outlining techniques you use to prioritize tasks, manage time effectively, and ensure that each study meets its deadlines without compromising quality. Mention tools or strategies that help keep you organized.

Provide an example that reflects your adaptability. Discuss the change and how you adjusted your plans accordingly, focusing on maintaining smooth operations and ensuring the research's integrity was preserved.

Discuss your views on how technology enhances efficiency, accuracy, and participant engagement in clinical research. Give examples of technological innovations you've encountered, such as mobile health applications or online data collection platforms.

Effective communication is key. Talk about maintaining regular contact through status updates, meetings, and reporting. Mention how you encourage feedback from team members and communicate emergent issues promptly.

Share your passion for advancing medical research and helping patients. Explain how the chance to contribute to innovative treatments and therapies motivates you to excel in your work as a Clinical Research Coordinator.