Clinical Research Coordinator - Cancer Institute at Memorial Regional Medic at Bon Secours Mercy Health

Midlothian, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

27 Jun, 26

Salary

0.0

Posted On

29 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Affairs, Clinical Research, IRB Submissions, FDA Compliance, ICH-GCP Knowledge, Data Capture, Serious Adverse Event Reporting, Regulatory Submissions, Attention To Detail, Organizational Skills, Communication, Critical Thinking, Problem-Solving, Microsoft Office Proficiency, Clinical Trial Management Systems, Electronic Regulatory Systems

Industry

Hospitals and Health Care

Description

Thank you for considering a career at Bon Secours! Scheduled Weekly Hours: 40 Work Shift: Days (United States of America) Primary Function/General Purpose of Position To implement and manage aspects of all active clinical research programs and to assist in other activities as assigned by investigator providers related to these programs with responsibilities to include, but not limited to: interacting with BSHSI legal, finance, compliance, and other departments as appropriate to help start up new clinical trials. Handle consents and agreements, capture patient data and enter it into confidential data management systems provided by industry sponsors, handle regulatory (IRB) submissions for new clinical trials, submit Serious Adverse Event (SAE) information to IRBs, handle amendments, manage safety reports and submit to IRBs as appropriate, track annual review dates and submit continuing reviews, and assist with departmental needs as requested in a back-up capacity. Requirements and Qualifications Bachelor’s degree in a health science, life science, or related field Minimum of 2 years of experience in regulatory affairs or clinical research Familiarity with regulatory and ethical requirements related to human subjects research (e.g., IRB, FDA, ICH-GCP) Strong attention to detail and organizational skills Excellent written and verbal communication. Ability to manage multiple priorities and meet deadlines Critical thinking and problem-solving abilities. Proficiency in Microsoft Office and familiarity with regulatory databases Preferred Requirements and Qualifications Master’s degree or regulatory certification (e.g., SOCRA, ACRP) Experience working in an academic medical center or large research institution Knowledge of electronic regulatory systems and clinical trial management systems (e.g., OnCore, REDCap) Bon Secours is an equal opportunity employer. As a Bon Secours 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 insurances, 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. Department: Clinical Research Richmond Oncology It is our policy to abide by all Federal and State laws, as well as, the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). Accordingly, 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 Mercy Health– Youngstown, Ohio or Bon Secours – Franklin, Virginia; Petersburg, Virginia; and Emporia, Virginia, which are Affirmative Action and Equal Opportunity Employer, please email recruitment@mercy.com. 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 recruitment@mercy.com. We believe your best is yet to come. At Bon Secours, we celebrate the human side of health care, uniting individuals from all walks of life. We'll ask a lot of you, but we'll give a lot back, as well. Whether you’re called to bedside care, patient support, community service or operations and administration, there’s a place for you here. Because if there's one thing we know for certain, it's that good works start with great people. We’ll support and empower you to bring your best – in service of our patients and our Mission.

Responsibilities

The primary function involves implementing and managing all active clinical research programs, which includes interacting with legal, finance, and compliance departments to initiate new clinical trials. Responsibilities also cover handling consents, capturing and entering patient data, and managing all necessary regulatory submissions, amendments, and safety reports to the IRB.