Clinical Research Assistant I- Angelman Syndrome - Boston Children's Hospital
Boston, MA
About the Job
***Position requires a cover letter***
*** Start date of June 2025 or soon thereafter***
The Division of Genetics and Genomics is seeking a Clinical Research Assistant to assist with clinical research projects that focus on Angelman syndrome in both children and adults. These projects include multiple industry-sponsored clinical trials.
This position may offer candidates an opportunity to shadow physicians and other healthcare providers in an academic medical center.
This Clinical Research Assistant I will be responsible for:
In order to qualify, you must have:
*** Start date of June 2025 or soon thereafter***
The Division of Genetics and Genomics is seeking a Clinical Research Assistant to assist with clinical research projects that focus on Angelman syndrome in both children and adults. These projects include multiple industry-sponsored clinical trials.
This position may offer candidates an opportunity to shadow physicians and other healthcare providers in an academic medical center.
This Clinical Research Assistant I will be responsible for:
- Assisting Principal Investigator (PI) in planning and implementing clinical research studies as assigned, including: coordinating preparation of protocol applications for submission to the IRB, study sponsor, regulatory authority, etc.; corresponding with the IRB, study sponsors, clinical research organizations, study participants, and referring physicians.
- Recruiting study participants for enrollment in clinical studies, including organizing strategies for recruiting study participants, screening study participants for eligibility, and completing informed consent procedures.
- Organizing study procedures and scheduling study participants for study visits. Assists the PI during study visits.
- Completing record abstraction of source documents, conducting required study measurements and completing study Case Report Forms (CRFs); conducting a QC check of completed CRFs prior to submission for data entry; coordinating resolution of all data queries.
- Maintaining regulatory binders, case report forms, source documents, and other study documents; monitoring the occurrence of adverse events and reporting to the PI, the study sponsor and the IRB, if any.
- Under the supervision of the PI, work with study staff to prepare for monitoring and audits by independent monitors, sponsors, and other regulatory agencies.
- Collection or processing of study specimens, delivery to appropriate labs or packaging and shipping to appropriate facilities.
- Assist PI and other study staff with conference presentations and manuscripts by extracting and compiling data from investigator-initiated studies
In order to qualify, you must have:
- Bachelor’s degree from an accredited 4-year college or university with a major in the sciences, engineering, mathematics, or psychology
- Strong quantitative and analytical skills; comfortable with numbers
- Interested 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.
- Ability to make a 2-year commitment
- At least one semester of basic science or clinical research experience preferred
- Defended an honors thesis or equivalent preferred
- Previous leadership position in student or community organizations preferred
Source : Boston Children's Hospital