The Ohio State University
Clinical Research Specialist I
This job is now closed
Job Description
- Req#: R107434
- 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.
Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. 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 l og 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:
Job Title:
Clinical Research Specialist IDepartment:
Medicine | PsychiatryClinical Research Specialist 1 is a supportive resource in the Department of Psychiatry and Behavioral Health, executing assigned clinical research studies using approved protocols administered by the Department of Psychiatry and Behavioral Health.
Research populations will include Spanish-speaking families. The candidate may be responsible for regularly communicating with Spanish-speaking research participants, including describing the research study, answering questions about the study, and completing recruitment and enrollment processes with Spanish-speaking participants.
The Clinical Research Specialist 1:
evaluates and implements design ated aspects of new research strategies;
participates in developing and implementing processes for patient data management;
collaborates with the Principal Investigator to develop and implement study participant consenting processes to comply with sponsor and federal regulations; develops and implements plans to meet requirements of new studies;
oversees and manages planning, implementation, and execution of data protocols from adolescent substance use research studies;
plans and supervises daily data management activities of the clinical research staff;
supervises clinical research data collection, management, and reporting;
collaborates with investigators to develop research protocols and assists with writing and preparation of grant applications to obtain research funding;
participates in lead writing and submission of manuscripts and articles for publication and presentation;
assists with activities to ensure compliance with Institutional Review Boards (IRB);
conducts quality assurance reviews of research processes and data;
ensures compliance with federal, state, and local regulations and guidelines; plans, coordinates, and participates in site visits by research sponsors and regulatory agencies as needed;
recruits, hires, trains, evaluates, and directly supervises clinical research staff; experience in crisis prevention and management.
Minimum Education Required: Bachelor's Degree with a Major in psychology, neuroscience, biological sciences, or healthcare administration.
Required Qualifications : Bachelor's Degree in psychology or neuroscience; knowledge of clinical research regulations, guidelines & compliance issues required, including Institutional Review Board (IRB) & federal or industry sponsor processes and requirements; supervisory experience preferred; experience with large datasets , storage, and NDA sharing strongly preferred; experience in clinical research in adolescent substance use and social determinants of health strongly preferred; experience writing research grants and proposals strongly desired; knowledge of medical terminology desired; computer skills required with experience using Microsoft Software and R studio applications desired. Requires successful completion of a background check. Selected candidates may be requested to complete a pre-employment physical, including a drug screen.
Research populations will include Spanish-speaking families. The candidate may be responsible for regularly communicating with Spanish-speaking research participants, including describing the research study, answering questions about the study, and completing recruitment and enrollment processes with Spanish-speaking participants.
Function: Research and Scholarship
Sub Function: Clinical Research
Career Band: Individual Contributor Series -Specialized
Career Level: S1
Additional Information:
Location:
Pelotonia Research Center (1040)Position Type:
RegularScheduled Hours:
40Shift:
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 Ohio State University is an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability, ethnicity, gender identity or expression, genetic information, HIV/AIDS status, military status, national origin, race, religion, sex, gender, sexual orientation, pregnancy, protected veteran status, or any other basis under the law.
Applicants are encouraged to complete and submit the Equal Employment Identification form.
About the company
The Ohio State University, commonly Ohio State or OSU, is a public land-grant research university in Columbus, Ohio.