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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. Position Summary: Under minimal guidance, this position is responsible for oversight of a portfolio of research projects. This position will lead the development and implementation of clinical research projects by collaborating with Principal Investigator and/or designees to ensure targets are met on time.
Job Responsibility:
Oversight of a portfolio of research projects
Lead the development and implementation of clinical research projects
Develop and implement enrollment strategies and study documents including protocol, and study manuals
Provide analytical, data management, and methodological support in the development of clinical research protocols and data management tools
Assist with the development and implementation of best practice guidelines for conducting various clinical research protocols
May train lab staff members and assist in writing articles and papers for submission
In conjunction with the PIs and/or designees designs, develops, and implement clinical research projects such as enrollment strategies, study materials, and study documents
Assist in writing grants
Prepare new applications for research funding and implementing and managing ancillary study grants
Responsible for daily operations of the study
Develops and implements processes and procedures to meet study goals and protocol requirements
Participate in training and prepare study related training materials
Plans and prioritizes the work of administrative and support personnel on all clinical study activities
Consents and enrolls patients for research studies by providing detailed information on the Clinical Study to patients and families
Communicates all policies and procedures and responds to all inquiries
Ability to interpret and apply clinical terminology to evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study
Provide input for updates of SOPs and drafting of new quality documentation
Assist with developing and implementing best practice guidelines for conducting various clinical research protocols
Presents and prepares training materials as part of the sponsored educational efforts
Provides analytical, data management, and methodological support to PIs in the development of clinical research protocols and data management tools
Manages data for single and/or multi-institutional investigations
Develops study specific data management and quality assurance procedures and monitors their implementation at site visits and/or periodic review of study data management reports
Works with PIs and lab members to plan analyses, clean and verify data and facilitate preparation of datasets for analyses
Requirements:
Bachelor’s Degree is required
Master’s or a higher level degree is preferred
Bachelor’s with 4 years of relevant work experience
OR Master’s level degree and 2 years of relevant work experience is required
Applicants with medical degrees are strongly encouraged to apply
Experience in advanced analytics or programming (R, Python) is preferred, though not required
Strong writing skills to assist with grants and manuscripts
Nice to have:
Experience in advanced analytics or programming (R, Python)
Master’s or a higher level degree
Medical degree
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