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Clinical Research Coordinator
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Hunterdon Hematology Oncology
Flemington, NJ (In Person)
Full-Time
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Job Description
Clinical Research Coordinator Hunterdon Hematology Oncology - 3.5 Flemington, NJ Job Details Full-time $45,000 - $65,000 a year 2 days ago Benefits Health insurance Dental insurance Paid time off Employee assistance program Vision insurance 401(k) matching Professional development assistance Life insurance Qualifications Clinical research Bachelor's degree Data management Budgeting Oncology Full Job Description Hunterdon Hematology Oncology is a private medical practice that specializes in chemotherapy, infusions, and radiation treatments, as well as innovative treatments like immunotherapy and personalized targeted therapy to provide the best possible outcomes for our patients. Our clinical research department conducts interventional and observational hematology and oncology clinical trials. We are looking for a candidate who is organized, adaptive, and has the capacity to work on a dynamic team. This is an excellent opportunity for someone who has been working in the field and is seeking advancement in their career. Candidates should have a minimum of 1 year of experience working in a clinical trial setting and be comfortable performing the following functions: Coordinating the activation and maintenance of multiple Hematology/Oncology Phase II-IV clinical trials, under the supervision of the Principal Investigator. Attending regular meetings with pharmaceutical corporations regarding pipeline clinical trials and preparing for all site qualification visits and site initiation visits with detailed agendas and proactive protocol-related questions. Completing annual IRB applications and assisting with new/amended clinical trial contracts/budgets. Screening potential subjects on the electronic medical record (EMR) and organizing all necessary paper/electronic source documentation for data management purposes. Generating monthly reports to actively screen and recruit eligible study subjects. Conducting the initial consent visit and all other study visits in adherence with the study protocol. Reporting any adverse events (AEs) and serious adverse events (SAEs) to research sponsors and all principal/sub-investigators in a timely manner. Finalizing case report forms (CRFs) with relevant study data, and addressing all pending queries according to sponsor guidelines. Collaborating with the research team and physician investigators regarding all clinical trial updates. Processing biologic samples, operating a centrifuge. Special consideration for candidates with oncology experience, however it is not a requirement. We are eager to add an organized, compassionate, and dedicated professional to our program.