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Clinical Research Specialist 2

The Ohio State University - Columbus, OH

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Job Description

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact . If you have questions while submitting an application, please review these frequently asked questions. Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required. Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application. Job Title: Clinical Research Specialist 2 Department: Dentistry | Periodontology The Ohio State University College of Dentistry is looking for a post-doctoral dentist for one-year research fellow position, effective immediately. The candidate will be expected to perform clinical as well as pre-clinical dental ultrasound studies. In addition to performing experiments, the fellow will analyze and present data, prepare manuscripts, assist in preparation of grant reports, and participate in research group data discussions. The Clinical Research Specialist coordinates and performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol; participates in the collection, processing & evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements. This position is contingent upon continued grant funding. Pay Range $24.76 - $32.33/hour based on relevant experience and education. Work Schedule Monday - Friday 7:30 a.m. - 4:30 p.m. Physical Requirements Work is performed primarily in an office environment and the employee in this position is subject to indoor environmental conditions. This position requires sustained periods using a keyboard and performing other computer work as well as reviewing documents both in hard copy and electronic formats. Requires sufficient personal mobility and physical reflexes, which permits the employee to function in a general office environment to accomplish tasks. This position requires successful completion of a criminal background check and drug and alcohol screening. Required Experience/Education Required: 1 year of performing clinical research, dental digital workflow, periodontal/implant surgeries are also required. Bachelor's Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education and/or experience. Preferred Experience/Education A dental degree (DDS), either granted by a CODA-accredited Dental School in the United States or by a foreign Dental School. 2-4 years of relevant research experience preferred in surgical dentistry, such as performing periodontal and implant surgeries and understanding of interpreting dental ultrasound images or demonstrate the ability to do so. A degree in dental radiology is desirable. A related masters or PhD degree will be given preference. The candidate should have research experience on using software and the dental digital workflow, e.g., 3D Slicer, Osirix/Horos, Blue Sky Bio, 3-D printing, etc. Additional Information:Location: Postle Hall (0024) Position Type: Regular Scheduled Hours: 40 Shift: First Shift Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process. Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions. The university is an equal opportunity employer, including veterans and disability. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.

Created: 2026-03-04

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