Clinical Research Coordinator - Cancer Control

The Ohio State University Wexner Medical Center

United States

On-site

USD 55,000 - 75,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental and vision coverage
Paid time off (vacation/sick)
State retirement plan

Job summary

The Ohio State University Wexner Medical Center's University Hospital seeks a Clinical Research Coordinator for the Cancer Control Department to oversee daily clinical research activities within the Clinical Trials Office.

Responsibilities include screening patient records, recruiting and enrolling participants, obtaining informed consent, coordinating visits, monitoring adverse events, and ensuring IRB and regulatory compliance.

Qualifications

  • Bachelor’s degree in biological sciences, health sciences, social sciences, or other medical field or equivalent combination of education and experience.
  • One year of experience in a clinical research capacity is required.
  • Knowledge of medical terminology desired.
  • Clinical research certification from an accredited certifying agency desired.
  • Computer skills with Microsoft Office applications desired.
  • Effective communication with clinical staff, research participants, and collaborators.

Responsibilities

  • Assist with assessing patient records to identify patients eligible for specified clinical research protocols.
  • Recruit, interview and enroll patients.
  • Obtain informed consent and ensure consent process complies with regulations.
  • Educate patients and families about purpose, goals, and processes of the study.
  • Coordinate scheduling and follow-through of patient care appointments and testing per protocol.
  • Monitor patients for adverse reactions and notify appropriate professionals as needed.
  • Document unfavorable responses and notify sponsors and regulatory agencies.
  • Assist with collecting, extracting, coding, and analyzing clinical research data.
  • Support compliance with IRB, FDA, and sponsor regulations.
  • Coordinate and prepare for external QA and IRB reviews.

Skills

Communication
Microsoft Office
Clinical research experience

Education

Bachelor’s degree in biological/health/social sciences or related field
Clinical research certification (desirable)

Tools

Microsoft Office

Job description

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 Coordinator - Cancer Control Department: CCC | Clinical Trials Office
Position Summary

The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Recruitment, Intervention and Survey Shared Resource, a part of the Clinical Trials Office within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center.

Responsibilities
  • Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
  • Recruit, interview and enroll patients
  • Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements
  • Educate patients and families of purpose, goals, and processes of clinical study
  • Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with the study protocol
  • Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate patient response, identify the status of complications, & provide the appropriate level of care
  • Document unfavorable responses and notify research sponsors & applicable regulatory agencies
  • Assist with collecting, extracting, coding, and analyzing clinical research data
  • Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry sponsor regulations
  • Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
  • Participate in activities to develop new research protocols and contributes to the establishment of study goals to meet protocol requirements
Job Requirements
  • Bachelor’s Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required.
  • One year of experience in a clinical research capacity is required.
  • Knowledge of medical terminology desired.
  • Clinical research certification from an accredited certifying agency desired.
  • Computer skills required with experience using Microsoft Office Software applications desired.
  • Must be able to effectively communicate, both face-to-face and in writing, with clinical staff, research participants, and outside collaborators.
Location

University Hospital - Pavilion (0372)

Position Type & Hours & Shift
  • 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.

The university is an equal opportunity employer, including veterans and disability.

Ohio State benefits give you options to take care of what matters most to you - and opportunities to make adjustments as your life and needs change, including:
  • Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
  • Paid time off, including sick and vacation time and 11 holidays.
  • State retirement plan or an alternative retirement plan, both with generous employer contributions.

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. At Ohio State, you'll find work that inspires you. We offer roles and growth opportunities in countless fields and specialties - including a job that's right for you. As Buckeyes, we accomplish more together. No matter your role, you'll be part of creating what people need now: pathways to education, research and health care. Working at Ohio State means you're part of a team with a strong sense of community and an unwavering commitment to excellence - and, of course, incomparable Buckeye spirit. We bring out the best in people, help each other succeed and learn together. By joining Ohio State, you become part of a top-20 public university with one of America's leading academic health centers. We're a team of dedicated colleagues with access to boundless resources that support you. Review the Frequently Asked Questions for details on using Workday and submitting your application.

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