Clinical Research Coordinator I
About The Position
Work as a Clinical Research Coordinator I (CRC I) in the MGB AMC Pediatric Neurotherapeutics and Psychopharmacology Clinical and Research Program under the supervision of the Program Director, Program Associate Director, Director of the Bressler Program for Autism Spectrum Disorder and Director of Pediatric Depression Research. In this presently hybrid role working within clinical and research settings, the coordinator will contribute to a range of research studies focused on understanding, predicting, diagnosing and treating mental health disorders in children. The CRC's main responsibilities will include investigations into the pharmaceutical and nutraceutical treatment of depression. The CRC will also assist with other projects researching emotional dysregulation, mood disorders, autism, and ADHD. The incumbent must be self-motivated, mature, and responsible with excellent organizational, as well as oral and written communication skills. Previous experience working in clinical trials is valued but not required. Must have excellent attention to detail. Must be able to work independently in a dynamic environment, juggle and prioritize multiple tasks, feel comfortable working with clinical and non-clinical study populations, and seek assistance when appropriate. Must be able to take the initiative to solve problems. Will be expected to communicate with the hospital's Institutional Review Board (IRB) in the submission and updating of protocols and continuing reviews of active studies.
Requirements
- Must be self-motivated, mature, and responsible with excellent organizational, as well as oral and written communication skills.
- Must have excellent attention to detail.
- Must be able to work independently in a dynamic environment, juggle and prioritize multiple tasks, feel comfortable working with clinical and non-clinical study populations, and seek assistance when appropriate.
- Must be able to take the initiative to solve problems.
- Will be expected to communicate with the hospital's Institutional Review Board (IRB) in the submission and updating of protocols and continuing reviews of active studies.
Nice To Haves
- Previous experience working in clinical trials is valued but not required.
Responsibilities
- Collect & organize patient data
- Maintain records and databases
- Use software programs to generate graphs, reports and slide sets
- Manage the recruitment of patients for research trials
- Obtain patient study data from medical records, physicians, etc.
- Verify accuracy of study forms
- Update study forms per protocol
- Document patient visits and procedures
- Maintain regulatory binders according to current QA/QC procedures
- Interview study subjects
- Administer and score questionnaires
- Provide basic explanation of study and in some cases obtain informed consent from subjects
- Perform study procedures, which may include phlebotomy, running MRI scans, and PET scans
- Assist with study regulatory submissions
- Draft consent forms and protocols
- Verify subject inclusion/exclusion criteria
- Assist with manuscript writing and submission
- Perform administrative support duties as required
- Perform other duties as assigned
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
