This Clinical Research Specialist III will be responsible for:
Supervising daily operations of the Clinical Research Studies and building upon role of CRS II.
Providing analytical, data management and methodological support to Principal Investigators in the development of clinical research protocols and data management tools. Managing data for single and multi-institutional investigations.
Assisting the development and overseeing the implementation of best practice guidelines for conducting various clinical research protocols. Preparing and presenting data and training materials.
Training and directing the activities of staff and providing input on Performance Management.
Providing analytical, data management and methodological support to clinical investigators in the development of clinical research protocols and data management tools. Managing data for single and multi-institutional investigations.
Collaborating and consulting, independently, with investigators and their staff on the design, development, and conduct of their clinical research studies.
Working with study investigators and statisticians to plan analyses, clean and verify data and facilitate preparation of datasets for analyses.
Collaborating directly with stakeholders on the development and writing of grants and study protocols.
Preparing and presenting educational materials to train clinical research staff in clinical research best practices.
Developing study-specific data management and quality assurance procedures and monitoring their implementation at site visits and/or periodic review of study data management reports
Ensuring work is performed in conformance with established hospital, program, federal, and state policies and procedures.
To qualify, you must have:
The knowledge of theories, principles, and concepts typically acquired through completion of a Bachelor's degree in health science, public health, epidemiology or a closely related field; coursework in biostatistics or computerized analytic methods plus 7 years of work experience with Clinical Trials or a Masters degree with 3 years of experience in a public health, community health or clinical research setting.
The Institutional Centers for Clinical and Translational Research (ICCTR) at Boston Children's Hospital enables investigators to make significant contributions to the improvement of children's health.ICCTR's primary mission is to support Boston Children's investigators through step-by-step guidance on planning, designing, implementing, and reporting clinical and translational studies.
Please note: During a public health emergency, individuals in this role may be expected to take on additional duties to respond to organizational needs. Boston Children's Hospital offers competitive compensation and unmatched benefits, including an affordable health, vision and dental insurance, generous levels of time off, 403(b) Retirement Savings Plan, Pension, Tuition Reimbursement, cell phone plan discounts and discounted rates on T-passes (50% off). Discover your best.
Boston Children's Hospital is an Equal Opportunity / Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.
Internal Number: 3129986
About Boston Children's Hospital
Boston Children's Hospital is a 395-bed comprehensive center for pediatric health care. As one of the largest pediatric medical centers in the United States, Children's offers a complete range of health care services for children from birth through 21 years of age.