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The Ohio State University
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The Ohio State University
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Clinical Research Assistant
Apply
$60k-79k (estimate)
Full Time 3 Days Ago
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The Ohio State University is Hiring a Clinical Research Assistant Near Columbus, OH

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 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 Assistant

Department:

CCC | Sponsored Research

Clinical Research Assistant in the Lifestyle Lab in the division of cancer prevention and control at The Ohio State University Comprehensive Cancer Center. The Lifestyle Lab is led by principal investigator, health promotion and behavioral scientist Roberto Benzo, Ph.D., MS. The lifestyle lab aims to study how lifestyle behaviors influence cancer-related health outcomes and to develop innovative lifestyle interventions to prevent disease, improve health outcomes, and reduce health disparities.

This position is on-site 5 days per week with possibility of hybrid schedule in the future.

Responsibilities include:

* Coordinate daily activities and efforts of research projects and behavioral interventions

* Assists with undergraduate and graduate students, postdoctoral fellows, and advanced practice providers

* Completes study-specific trainings; attends study meetings; provides weekly updates and progress reports on study activities, including recruitment and follow-up activities; and other administrative duties as needed

* Assist with development and submission of IRB protocols

* Educates patients and their families of the purpose, processes, and goals of studies

* Identifies, assesses, recruits, consents, and enrolls participants onto clinical studies

* Ensures research studies are conducted in accordance with the study protocol and guidelines, policies, and requirements of OSUCCC

* REDcap development and management

* Familiar with the use of technology (e.g., Fitbit) and online platforms (e.g., myfitnesspal, MyChart) related to health and wellness

Minimum Required Qualifications

Bachelor's Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.

Preferred Qualifications

* Familiarity with electronic medical record documentation (EPIC), chart review, and abstraction of data

* Education and/or experience in public health, exercise science, psychology, dietetics, nutrition, human physiology

* Quantitative and qualitative data analysis

* Excellent communication and writing skills

* Highly organized and self-driven

Starting Pay: $20.00 / Hour

Position Mapping: Research and Scholarship - Clinical Research - Technical - T2

Additional Information:

70%: Coordinates research project activities, primarily in the area of cancer prevention and control; develops and implements screening and recruitment activities that are conducted at the various sites; identifies, assesses, recruits, consents, and enrolls participants into clinical studies; maintains and develops optimal working relationships with physicians and personnel at the study sites; ensures that the research study is conducted in accordance with the protocol and requirements of investigators and sponsoring agencies; develops screening and recruitment reports; coordinates retention of participants; conducts chart review and data abstraction from the electronic medical record; participates in audits; identifies, documents, and tracks protocol violations and adverse events.

10%: Completes forms and reports in a timely manner; maintains participant and screening tracking systems; conducts quality assurance checks of all study data and forms and provides study researchers with monthly reports; resolves data queries; communicates with the study monitor.

10%: Conducts follow-up activities with study participants; coordinates with participating sites to ensure follow-up activities are conducted in a timely manner; coordinates the collection and receipt of biological samples, if applicable.

10%: Attends study team meetings; provides weekly updates on study activities; other duties as assigned.

Location:

McCampbell Hall (0303)

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 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.

Job Summary

JOB TYPE

Full Time

SALARY

$60k-79k (estimate)

POST DATE

06/28/2024

EXPIRATION DATE

07/13/2024

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The following is the career advancement route for Clinical Research Assistant positions, which can be used as a reference in future career path planning. As a Clinical Research Assistant, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Assistant. You can explore the career advancement for a Clinical Research Assistant below and select your interested title to get hiring information.

If you are interested in becoming a Clinical Research Assistant, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Clinical Research Assistant for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Clinical Research Assistant job description and responsibilities

Certifications are also available for this position through The Society of Clinical Research Associates (SOCRA) and The Association of Clinical Research Professionals.

01/04/2022: Santa Barbara, CA

Analyze and evaluate clinical data gathered during research.

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Provide regular report updates of the progress of clinical studies to the appropriate personnel.

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These clinical trials are very much regulated and seriously monitored to ensure that they comply with the laid down regulations.

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Must be able to ensure that data gotten from clinical trials are accurate and reliable and the legal rights and privacy of the subjects are protected.

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Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Clinical Research Assistant jobs

Fact-checking, editing, and proofreading research documents for accuracy and consistency.

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Research Assistants provide support to research teams who are conducting experiments or gathering and analysing data.

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Maintained FDA clinical trial documentation for department and received excellent FDA audits of records.

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Have strong customer focus and good communication skills

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For example, clinical research associate candidates should have excellent attention to detail and organizational skills since they’re responsible for monitoring and reporting on the results of clinical trials.

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