Boston Children’s Hospital
Senior Clinical Research Coordinator- Angelman Syndrome
Boston Children’s Hospital, Boston, Massachusetts, us, 02298
Position Summary
The Division of Genetics and Genomics at Boston Children’s Hospital is seeking an experienced Clinical Research Coordinator to assist with clinical research projects that focus on Angelman syndrome in both children and adults. The primary role will be to oversee the operations of a large investigator-initiated, multi‑center natural history study of Angelman syndrome.
Key Responsibilities
Assisting Principal Investigators (PI) with designing and implementing clinical research protocols, including coordinating the preparation of protocol applications for Institutional Review Board (IRB) submissions, managing stakeholder contracts, ensuring regulatory compliance across study sites, and overseeing the day-to‑day activities of the study.
Delivering regular updates and progress reports to PIs and sponsors, including organizing and leading steering committee sessions focused on continuous improvement.
Conducting virtual and in‑person study site visits (pre‑study, initiation, monitoring, and close‑out) and ensuring sites complete deliverables within given timelines.
Maintaining multiple study databases by coordinating data entry and updates, optimizing data retrieval processes, and enhancing user interface and system performance.
Reviewing and verifying study data for(State) accuracy and completeness.
Creating and implementing subject recruitment and enrollment strategies for study sites.
Developing case report forms (CRFs), protocols, training manuals, and other study‑related documents.
Preparing conference presentations and manuscripts by cleaning and preparing datasets for analyses.
Minimum Qualifications Education
Bachelor’s Degree required, Master’s Degree preferred
Experience
Bachelor’s Degree with 4 years of relevant work experience; OR Master’s Degree and 2 years of relevant work experience
Strong quantitative and analytical skills, including use of statistical software and programming languages such as R or Python
Interest in working with children and adults with severe physical and intellectual disabilities, and their families
Excellent interpersonal as well as oral and written communication skills
Willingness to work flexible hours, as and when required
#J-18808-Ljbffr
Key Responsibilities
Assisting Principal Investigators (PI) with designing and implementing clinical research protocols, including coordinating the preparation of protocol applications for Institutional Review Board (IRB) submissions, managing stakeholder contracts, ensuring regulatory compliance across study sites, and overseeing the day-to‑day activities of the study.
Delivering regular updates and progress reports to PIs and sponsors, including organizing and leading steering committee sessions focused on continuous improvement.
Conducting virtual and in‑person study site visits (pre‑study, initiation, monitoring, and close‑out) and ensuring sites complete deliverables within given timelines.
Maintaining multiple study databases by coordinating data entry and updates, optimizing data retrieval processes, and enhancing user interface and system performance.
Reviewing and verifying study data for(State) accuracy and completeness.
Creating and implementing subject recruitment and enrollment strategies for study sites.
Developing case report forms (CRFs), protocols, training manuals, and other study‑related documents.
Preparing conference presentations and manuscripts by cleaning and preparing datasets for analyses.
Minimum Qualifications Education
Bachelor’s Degree required, Master’s Degree preferred
Experience
Bachelor’s Degree with 4 years of relevant work experience; OR Master’s Degree and 2 years of relevant work experience
Strong quantitative and analytical skills, including use of statistical software and programming languages such as R or Python
Interest in working with children and adults with severe physical and intellectual disabilities, and their families
Excellent interpersonal as well as oral and written communication skills
Willingness to work flexible hours, as and when required
#J-18808-Ljbffr