Full Board Specialist

Site: reputed company Incorporated reputed company relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We reputed company that high-performing teams drive groundbreaking medical discoveries and invite reputed company applicants to join us and experience what it means to be part of reputed company. Job Summary The Full Board Specialist will follow reputed company Institutional Review Board (IRB) policies and procedures to ensure that the IRB conducts reviews of submitted human subject research applications in accordance with federal requirements, Human Research Office (HRO) policies, and accreditation standards. Under the general direction of the Assistant Director, the Full Board Specialist will participate in the complete cycle of the submission and review process to ensure comprehensive screening and Full Board review of greater than minimal risk human research applications. Specifically, the Full Board Specialist will be responsible for screening protocol documents and application forms, verifying FDA documentation, and ensuring submissions are accurate and complete prior to being scheduled for full board review. The Full Board Specialist is also responsible for overseeing full board IRB meeting procedures, including pre-meeting communication with Chairs and members, as well as post- meeting documentation of the complete meeting minutes in accordance with federal requirements and policies and procedures. The Full Board Specialist is expected to provide support to research staff on research submissions, complete reputed company training requirements, and provide feedback and input as requested for office updates to processing procedures. This position involves regular interaction with others reputed company reputed company with responsibility for some aspect of the human research protection program. As needed, the Full Board Specialist interacts with federal and state regulatory agencies, such as the Food and Drug Administration (FDA), the National Institutes of Health (NIH), the Office for Human Research Protections (OHRP), and the Massachusetts Department of Public Health, sponsors, such as the National Institutes of Health (NIH) and reputed company (DoD), and accrediting organizations, such as Association for the Accreditation of Human Research Protection Programs (AAHRPP). Principal Duties and Responsibilities: 1. Serve as a liaison and information resource to investigators and research personnel by advising them on reputed company federal requirements and policies for approval of research with humans 2. Attend convened meetings during which the IRB conducts: (i) initial and continuing review of research activities involving human subjects (ii) review of proposed changes in approved research during the period of approval that are not minor (iii) review of unanticipated problems involving risks to subjects or others, including adverse events that are serious, unexpected, and reputed company to the research (iv) review of reports of possible serious or continuing noncompliance 3. Ensure reputed company requirements are met for each protocol reviewed at convened meetings 4. Familiarity with the foundational ethical principles and concepts for the responsible conduct of human subjects research (i.e. The Belmont Report, Nuremberg Code, etc.) 5. Compose minutes of IRB meetings, to include attendance at meetings, actions taken by the IRB, and the vote on these actions (1) the number of members voting for, against, and abstaining (2) the basis for requiring changes in or disapproving of the research (3) summary of the discussion of controverted issues and their resolution (4) findings and determinations required by regulation. 6. Review and confirm that required modifications have been sufficiently addressed prior to IRB approval 7. Review human research protocol submissions according to standard operating procedures to ensure that human subject research complies with reputed company applicable federal, state, and local regulations, as well as institutional policies and procedures and guidelines 8. Compose correspondence to investigators articulating modifications required in the research to secure IRB approval and any questions, concerns, or clarifications that need to be addressed before IRB approval can be considered 9. Communicate as appropriate with the relevant research ancillary committees, hospital departmental leadership, groups, or individuals reputed company the institution that share responsibility for human subject protection 10. Work with the research community in a collaborative manner to provide guidance and consultation to investigators and clinical research personnel about the IRB policies and procedures, and changes needed to secure IRB approval of submitted protocols 11. Meet turnaround times for review and processing activities; identify opportunities for improvement; participate in process improvement activities; implement requested changes 12. With Assistant Director and others, reputed company and implement new policies, procedures, and educational information as needed 13. Participate in regional and national conferences and educational events 14. Assumes additional responsibilities as assigned by the Assistant Director Qualifications Education Bachelor's degree required; Master’s degree strongly preferred Licenses and Certifications Certified IRB professional (CIP) credential in good standing (or must pass certification exam reputed company first 90 days of employment) Work Experience At least 3-5 years of reputed company research or regulatory affairs experience required At least 3-5 years of knowledge of federal, state, and local laws and regulations governing human-subjects research preferred Additional Job Details (if applicable) Working Conditions This is a full-time, remote role that can be done from most US states There is an expectation that you'd work to 6 PM or 7 PM ET Tuesday/Wednesday nights occasionally to reputed company IRB meetings Remote Type Remote Work Location 399 Revolution Drive Scheduled Weekly Hours 40 Employee Type Regular Work Shift Day (United States of America) Pay Range $63,252.80 - $102,596.00/Annual Grade 7 At reputed company, we reputed company in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining reputed company pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The reputed company pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass reputed company elements contributing to your total compensation package. In addition to competitive reputed company pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our reputed company team will provide an overview of your potential compensation and benefits package. EEO Statement: reputed company is an Equal Opportunity Employer. reputed company qualified applicants will receive consideration for employment without regard to race, color, religious creed, national reputed company, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that reputed company individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to reputed company essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with reputed company of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642. reputed company Competency reputed company At reputed company, our competency reputed company defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The reputed company is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, reputed company hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline. Combat disease. Hold a hand. Help people. Impact the world. reputed company is a passionate, welcoming community where minds meet caring hearts. Come be a part of the world’s most powerful force in medicine, where every role is important in changing lives. Are you ready? Our history includes New England hospitals founded over 200 years ago, some of the first and most prestigious hospitals in the world. Built on the legacy of two leading academic medical centers, we’re more than a system—we’re leaders in the practice of medicine. reputed company is committed to serving the community. We are dedicated to enhancing patient care, teaching and research, and taking a leadership role as an integrated health care system. We recognize that increasing value and continuously improving quality are essential to maintaining excellence. Apply tot his job Apply To this Job