DescriptionWhy RTI RTI International (RTI) is both a global research institute and a leading international development organization based out of North Carolina. At RTI, you will find work you believe in, tackling some of the most complex global challenges of our time. Our mission is to impact the wellbeing of 1 billion people by 2030 through science-based solutions in climate, education, health, and equity. Our staff promote meaningful change around the world helping people live healthier, more productive, and more independent lives. If you are looking for an opportunity to make a real difference, RTI is the place for you. Join us in our commitment to teamwork, belonging, and the passion to change the world. About the Hiring Group RTI is seeking a Clinical Trials Coordinator in the Clinical Project Management (CPM) program. The CPM program delivers innovative project management and operational support solutions for broad-based research including multisite studies, clinical networks and related collaborative public health efforts. The ideal candidate will be highly motivated, results-oriented, and collaborative with experience working as an integral member of a multi-site clinical trial operations team. The Clinical Trials Coordinator will support study teams for clinical trials and Data Coordinating Center projects with tasks pertaining to study planning, communication, budget and resource management. What You'll Do The key deliverables for this role are to assist and support in the planning and execution of clinical trials and Data Coordinating Centers. Assist in the distribution of study documents and materials including data collection forms, manuals of operations and technical memos to research sites. Distribute various materials, including study supplies and data collection forms, to clinical sites. Coordinate and schedule conference calls; write and distribute meeting minutes. Assist with management of correspondence and project communications. Assist in the preparation and updating of progress reports and client/study/network meeting materials. Assist in the preparation and maintenance of IRB documents. Participate in quality control activities. Gather background data and information to support proposal and project efforts. What You'll Need Job Requirements are a combination of qualifications and related experience. Judgment of an acceptable equivalent combination, on an individual basis, is the responsibility of Management. Bachelor's Degree in Clinical Research and 0 years of experience, or equivalent combination of education and experience. Prior internship in the clinical trials field. Certification(s) in Human Subjects Research Training and/or Good Clinical Practices Proficiency with MS Word, Outlook, PowerPoint, Excel. Demonstrated interest in clinical research. Ability to work in a highly collaborative environment. Ability to listen and communicate well both verbally and in writing. Ability to synthesize and summarize complex information. Attention to detail and accuracy. Ability to handle regular changes to priorities, interruptions to independent work due to meetings, and multiple tasks ongoing simultaneously. EEO & Pay Equity Statements For San Francisco, CA USA Job Postings Only: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Further information is available here. RTI accepts applications to our job openings from candidates with criminal histories or conviction records in accordance with all applicable laws, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. For Applicants in Massachusetts Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. The anticipated pay range for this role is listed below. Our pay ranges represent national averages and may vary by location as a geographic differential may be applied to some locations within the United States. RTI considers multiple factors when making an offer including, for example: established salary range, internal budget, business needs, and education and years of work experience possessed by the applicant. Further, salary is merely one element to our offer. At RTI, we demonstrate our commitment to rewarding individual and team achievement through a total rewards package. This package includes (among other things) a competitive base salary, a generous paid time off policy, merit based annual increases, bonus opportunities and a robust recognition program. Other benefits include a competitive range of insurance plans (including health, dental, life, and short-term and long-term disability), access to a retirement savings program such as a 401(k) plan, paid parental leave for all parents, financial assistance with adoption expenses or infertility treatments, financial reimbursement for education and developmental opportunities, an employee assistance program, and numerous other offerings to support a healthy work-life balance. Equal Pay Act Minimum/Range $66,000 - $82,000
ResponsibilitiesThe key deliverables for this role are to assist and support in the planning and execution of clinical trials and Data Coordinating Centers. Assist in the distribution of study documents and materials including data collection forms, manuals of operations and technical memos to research sites. Distribute various materials, including study supplies and data collection forms, to clinical sites. Coordinate and schedule conference calls; write and distribute meeting minutes. Assist with management of correspondence and project communications. Assist in the preparation and updating of progress reports and client/study/network meeting materials. Assist in the preparation and maintenance of IRB documents. Participate in quality control activities. Gather background data and information to support proposal and project efforts
QualificationJob Requirements are a combination of qualifications and related experience. Judgment of an acceptable equivalent combination, on an individual basis, is the responsibility of Management. Bachelor's Degree in Clinical Research and 0 years of experience, or equivalent combination of education and experience. Prior internship in the clinical trials field. Certification(s) in Human Subjects Research Training and/or Good Clinical Practices Proficiency with MS Word, Outlook, PowerPoint, Excel. Demonstrated interest in clinical research. Ability to work in a highly collaborative environment. Ability to listen and communicate well both verbally and in writing. Ability to synthesize and summarize complex information. Attention to detail and accuracy. Ability to handle regular changes to priorities, interruptions to independent work due to meetings, and multiple tasks ongoing simultaneously