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At Boston Children’s Hospital, the quality of our care – and our inclusive hospital working environment – lies in the diversity of our people. With patients from local communities and 160 countries around the world, we’re committed to reflecting the spectrum of their cultures, while opening doors of opportunity for our team. Here, different talents pursue common goals. Voices are heard and ideas are shared. Join us, and discover how your unique contributions can change lives. Yours included. The Clinical Research Coordinator will coordinate activities of daily operations for Dr. Stephanie Sacharow’s clinical research trials. Dr. Sacharow’s research focuses on Phenylketonuria in pediatric and adult patients. Dr. Sacharow’s research trials include drug trials and some focus on neurological imaging and neurocognitive tests. They will interact with patients at Boston Children’s Hospital diagnosed with Phenylketonuria. The ideal candidate will have clinical research experience, strong organizational and interpersonal skills, and the ability to prioritize and to perform multiple tasks. They must be able to work effectively on a team, as well as independently. Dr. Sacharow’s lab is looking for two-year commitment. This is an exciting opportunity to work within a multidisciplinary team furthering research and bringing new treatments to children and adults with rare genetic conditions. They will have direct patient-facing experience in providing patient care oversight. This role is ideal for those considering/pursuing graduate academia in patient sciences or those wanting to explore patient centered clinical research.
Job Responsibility:
Coordinate activities of daily operations for clinical research trials
Run study visits, which includes contacting patients/families, scheduling visits, preparing study materials/samples for shipment, and conducting monitor visits with study sponsors
Serve as liaison between BCH and study sponsors/CROs
Participate in the screening, consenting, recruitment, and selection of patients for studies
Prepare IRB and/or CCI documentation and submissions
Conduct data collection activities and prepare analytical reports regarding results of studies
Assist in writing articles and summary papers for various publications
Complete eCRFs/paper CRFs
Lead weekly/biweekly meetings to update the PI on study progression
Have leadership roles on Dr. Sacharow’s team for different studies
Assist with completing regulatory tasks including IRB submissions and study operations maintenance
Requirements:
Bachelor’s degree
2 years of relevant experience
Analytical skills to gather and interpret data
Excellent organizational skills and attention to detail
Resourcefulness to independently find answers and solve problems
Effective communication and writing skills
Ability to effectively deal with conflicting views or issues and mediate fair solutions
Knowledge of principles of study design and approaches to statistical analysis
Ability to problem-solve, create, implement, and evaluate clinical study operational needs
What we offer:
Flexible schedules
Affordable health, vision and dental insurance
Child care and student loan subsidies
Generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement