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.
Project Manager to plan, lead and manage implementation and execution of daily activities for multicenter clinical research studies in accordance with approved protocols and guidelines administered by the Department of Psychiatry and Behavioral Health in daily administrative and research operational activities between the Department of Psychiatry and Behavioral Health and national and international partners for joint research projects and grants; Collaborates with investigators to create, develop and implement new protocols, process and maintain IRB submissions and other regulatory documentation, explores and identifies feasibility of new studies and develops plans to meet protocol requirements, participates in development and application of research methodologies, develops communications amongst local coordinating center and subsites, coordinates regulatory compliance, data collection, and assists in development of training and certification materials; central meetings preparations; reviews, monitors and authorizes expenditures against research grant; serves as a liaison to subsites, state & federal regulatory agencies, and federal, industry & research sponsors; represents and promotes the goals and objectives of the study to various internal and/or external constituencies, as appropriate; assists with development, content and oversight of study websites & promotional materials, manages data collection, analysis & reporting; oversees and establishes assessment criteria and processes for determination of participant eligibility, recruitment and on-going support for study participants, develops processes & strategies to promote recruitment & retention; plans, coordinates and assigns daily activities to project staff, monitors and evaluates protocol activity to ensure compliance to all state, federal and sponsor policies, rules and regulations, prepares and participates in study monitoring visits, serves as liaison with IRB, FDA, drug companies and industry sponsors, assists with investigators with preparation of submission of grants to secure continued funding of research projects, collaborates with investigators to write abstracts, manuscripts, articles and research reports for publication in peer-reviewed journals, attends and presents research data at scientific meetings, serves a subject matter leader.
Duties Description:
40% Oversees, manages and coordinates implementation and execution of clinical research activities within the Department of Psychiatry & Behavioral Health program; ensures compliance with all local, state and national regulations; serves as primary resource for multi-site collaborative projects
30% Coordinates and prepares protocol applications, human subject and regulatory documents for IRB review; serves as a liaison with PI (s), IRB, other officials and sponsors as needed
25% Oversees and prepares for external quality assurance and control reviews; actively participates in site visits and audits; assists with study set up preparation including systems for data capture, quality assurance and data extraction; assists with training new staff members working on assigned studies
5% Provides support related to financial management of assigned projects.
Experience:
Bachelor's degree in biological or health sciences, or an equivalent combination of education & experience required; Master's degree preferred; considerable experience with planning and administering research projects required, preferably in a health services or clinical research study setting; proficiency with data abstraction required; clinical research certification from ACRP (Association of Clinical Research Professionals) or SOCRA (Society of Clinical Research Associates) certification is strongly desired; working knowledge of medical terminology required. Requires successful completion of a background check. Qualified candidates may be asked to complete a pre-employment physical including a drug screen and background check.
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.
More jobs in Columbus, Ohio
|
Worthington Industries Inc |
|
Worthington Industries Inc |
|
Kroger |