Research Coordinator - Columbus, Ohio | CareerCircle
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Research Coordinator



Posting ID: JP-002659674

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Columbus, Ohio
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*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.

Experience Level:

Entry Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Contact Information

Recruiter: Jared Swanson

Phone: +17639232066


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