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Investigator Research Assistant - St. Vincent Medical Center

Bon Secours Mercy Health

Toledo, OHResearchSeen 2w agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Toledo, OH
Role Type
Research
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Investigator Research Assistant supports investigator‑initiated studies at St. Vincent Medical Center by monitoring safety events, coordinating communications among study sites, vendors, and the central coordinating center, and handling administrative tasks such as contract management, budgeting, and document filing while assisting with study initiation visits and manuscript preparation.

Skills & qualifications

RequiredNice to have

Skills

Document ManagementMicrosoft OfficeTechnology KnowledgeManagement SkillsIndependent WorkTeam Collaboration

Qualifications

Bachelor's in Healthcare Research or Related Field1 Year Clinical Research Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off
Tuition Assistance

Full job description

Primary Function/General Purpose of Position

Responsible for assisting in all aspects of Investigator Initiated Studies coordinated through the central coordinating center.

Essential Job Functions

  • Act as a safety medical monitor when needed by reviewing and documenting the completion of the reviews of all clinical events and all serious clinical events recorded by the sites and provide a monthly report to the Central Coordinating Center (CCC) research team

  • Assist in facilitating communication with central statistical center, Data Safety Management Team, the study sites that are reporting to the CCC, third party vendor providing the electronic data to the CCC and to all sites, any needed third party subcontract to maintain services needed across all sites and with the third party vendor, core imaging center and assuring timely completion of the tasks

  • Reconcile and assist the manager in obtaining and completing the subcontracts from all the national research sites

  • Assist in site initiation visits with slides to illustrate the study and requirements, Remote and occasional on site monitoring that requires travel to the sites

  • Assist in Drafting and proof editing study abstract, meeting presentations, Submission of abstract to meeting website, Help and drafting of the paper/manuscript preparation, Double checking and performing statistical analysis as needed, submission of full paper to the journals

  • Responsible for assisting with the clinical administrative operations activities involving clinical contract and budget support including but not limited to filing, scanning, mailing, populating spreadsheets and other administrative tasks as assigned. Duties and functions include:

  • Filing the documentation obtained from all sites and maintaining it in accordance with regulatory and compliance rules as per FDA, and study regulations.

  • Perform Quality Control (QC) on the scanned contracts to ensure: All pages of the documents are included; all required signatures are verified and present; all budget pages are legible; and all documents have been saved in the Shared Folder for CCC team.

  • Assist with maintaining administration with the help of CCC team invoices from other sites. Work with financial analyst and manager to ensure the QC of the budgets and accounts. __

This document is not an exhaustive list of all responsibilities, skills, duties, requirements, or working conditions associated with the job. Employees may be required to perform other job-related duties as required by their supervisor, subject to reasonable accommodation.

Licensing/Certification

None

Education

Bachelor's Degree in healthcare, research, or related field (required)

Work Experience

1 year experience in clinical research, writing, draft clinical paper, abstract submission to scientific meetings, submission of full clinical research paper to journal, base stat knowledge and analysis (required)

Training

None

Language

None

Skills

Document management

Microsoft Office

Demonstrated knowledge of technology and its application to improving processes

Demonstrated management skills or experience

Ability to work independently with minimal supervision

Ability to work effectively as a team member

As a Bon Secours Mercy Health associate, you're part of a Mission that matters. We support your well-being—personally and professionally. Our benefits are built to grow with you and meet your unique needs, every step of the way.

What we offer

  • Competitive pay, incentives, referral bonuses and 403(b) with employer contributions (when eligible)

  • Medical, dental, vision, prescription coverage, HSA/FSA options, life insurance, mental health resources and discounts

  • Paid time off, parental and FMLA leave, short- and long-term disability, backup care for children and elders

  • Tuition assistance, professional development and continuing education support

Benefits may vary based on the market and employment status.

All applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, sexual orientation, gender identity, age, genetic information, or protected veteran status, and will not be discriminated against on the basis of disability. If you'd like to view a copy of the affirmative action plan or policy statement for Bon secours Mercy Health – Youngstown, Ohio or Bon Secours – Franklin, Virginia; Petersburg, Virginia; and Emporia, Virginia, which are Affirmative Action and Equal Opportunity Employers, please email [email protected] . If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact The Talent Acquisition Team at [email protected]

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