Posting ID: JP-002659674
*Works in collaboration with the Principal Investigator (PI) to coordinate industry-sponsored and investigator-initiated clinical trials *Develop relationships with patients as partners in their care *Collaborate with clinicians to plan and facilitate patient recruitment and retention *Coordinate communication with sponsors, partnering departments, vendors, and national agencies *Educate patients and study staff on research and trial specifics *Manage clinical and administrative study operations to ensure compliance with all IRB (Institutional Review Board), FDA (Food and Drug Administration), federal, state, and industry sponsor regulations *Adhere to study schedules and timelines *Maintain detailed documentation at patient and study level *Fulfill reporting requirements in accordance with timelines Shift: Monday - Friday 8 AM - 5 PM. Also have some flexibility, if someone wanted to work four 10's Monday - Thursday for example AFTER going through a 90 day training/onboarding period.
clinical trial, patient consent, patient electronic medical record emr software, patient information, irb, fda submissions, drug trials, medical device
Top Skills Details:
clinical trial,patient consent,patient electronic medical record emr software,patient information,irb
Additional Skills & Qualifications:
*Two years of direct clinical research experience (oncology experience is a big plus) *Applies critical thinking and creative problem solving skills across a wide variety of clinical studies *Ability to prioritize the work of multiple projects. *Experience in a team setting. *Strong verbal and written communication skills, as well as customer service skills and ability to problem solve, prioritize and manage multiple tasks *Strong computer skills, including thorough knowledge of systems (EMR, Microsoft) MUST INCLUDE SCREENING QUESTIONS BELOW: Screening Q's: Technical based: • Checking eligibility of patients? • Consenting patients? • Scheduling patients? • Observational or treatment (with drug) trials? • Observational or treatment (with medical device) trials? • How many trials carry at one time? • How many patients are part of workload? #? • Did patients come in for reoccurring visits- for example, cycle 1 day 1, cycle 2 day 3, etc? • What EDC systems have experience using? • Any experience with Epic as medical records system? • Experience with investigational drug studies? How much of it? Behavioral based: • Describe how you would handle a situation where a P.I. wanted to enroll a patient you didn’t think was eligible? • How would you handle a situation where you came in for your first day and your manager was called away? • Tell us something about yourself that is not on your resume.
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Recruiter: Jared Swanson