Okay, I've searched for Research Study Assistant roles in New Brunswick, NJ, prioritizing those that need proficiency in Epic and data entry, focusing on clinical research, and offering full-time positions. I have found 34 relevant positions for you.

Sure. Here's the analysis:

Job Analysis:

The role of a Research Study Assistant at Lensa focuses on ensuring the security and integrity of complex computerized records systems within the clinical research context, particularly in oncology. This person is fundamentally hired to support research operations by collaborating closely with clinical research coordinators and other medical staff to maintain accurate patient records and document data effectively. Primary responsibilities include data abstraction, entry into Case Report Forms or electronic systems, and conducting regular quality assurance activities. What’s crucial about these tasks is that accuracy and compliance with research protocols are essential for the integrity of the clinical trials. The ideal candidate will face challenges such as managing large volumes of data, resolving discrepancies, and ensuring that all entries meet the stringent standards of clinical research. Success in this role will likely manifest in the seamless management of patient data, timely reporting, and active participation in team discussions, contributing to the overall efficiency and integrity of ongoing clinical trials.

Company Analysis:

Lensa operates within the evolving landscape of career platforms, effectively using machine learning to transform how job seekers connect with opportunities. Positioned as a leading career site, the company's focus on putting people first demonstrates a commitment to innovation and efficiency in talent acquisition. This innovative spirit is reflected in their comprehensive and tech-driven approach to matching candidates with job openings. The culture at Lensa appears to be collaborative and detail-oriented, as indicated by the emphasis on teamwork and effective communication in the role. The Research Study Assistant will find themselves in a supportive environment that values accuracy and collaboration, working under the guidance of seasoned professionals in a hybrid work model, emphasizing flexibility. Strategic alignment is evident in this hire; the assistant's work is integral not only to maintaining the quality of research data but also in enhancing the organization’s capability to enroll thousands in clinical trials as it aims to expand its reach in oncology research. This role contributes directly to Lensa's mission of impactful job facilitation, streamlining the job search process for professionals.

Absolutely. Here are some mock interview questions that could come up:

• Tell me about a time when you had to manage a large amount of data accurately under pressure.
• Can you describe a situation where you identified a data discrepancy and how you resolved it?
• How do you prioritize multiple tasks when faced with tight deadlines?
• What steps would you take to ensure you comply with research protocols while managing study records?
• How would you approach entering patient data from charts into an electronic system?
• Can you explain your familiarity with medical terminology and how it relates to clinical research?
• Describe your experience with software programs such as Epic or Oncore and how they have assisted you in previous roles.
• Imagine you encounter conflicting information while conducting data abstraction. What would you do?
• What strategies would you employ to maintain organization and detail orientation in your work processes?
• Why are you interested in working at Lensa and specifically in this Research Study Assistant role?
• How do you see your values aligning with Lensa's mission to improve the job search experience?
• What do you believe is the most significant challenge facing clinical research today, and how might this role address it?
• In what ways do you think teamwork will impact the success of clinical trials in this role?
• What questions do you have about the collaboration process with the Disease Study Group members?
• How do you stay current with developments in clinical research and data management?