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Job Requirements of Clinical Research Coordinator II:
-
Employment Type:
Contractor
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Location:
Boston, MA (Onsite)
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Clinical Research Coordinator II
Careers Integrated Resources Inc
Boston, MA (Onsite)
Contractor
Job Title: Clinical Research Coordinator II
Location: Boston, MA 02118
Duration: 4 Months+ contract with possible Extension
Shift: Flexibility to start at 7 am if visits start early, 8 hours per day, Mon - Fri
Payrate: $30.00 - $35.00/ hr. on w2
Job Responsiblities-
Location: Boston, MA 02118
Duration: 4 Months+ contract with possible Extension
Shift: Flexibility to start at 7 am if visits start early, 8 hours per day, Mon - Fri
Payrate: $30.00 - $35.00/ hr. on w2
Job Responsiblities-
- Under the supervision of the Lead CRC, Senior Research Manager and Principal Investigator for assigned research studies, the Clinical Research Coordinator (CRC) will perform research activities using approved techniques.
- The CRC procures, processes and ships research specimens and conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks, assists in grant preparation, and participates with the research team in preparation of data and other reports.
- Will also assist with audits and quality improvement projects.
- Evaluating and tracking the eligibility of all patients seen in the clinic.
- Obtaining informed consent (for non-treatment studies) and registering patients to cohort studies and other protocols.
- Reviewing and abstracting the medical records for patients, including review of pathology reports.
- Accessing patient demographic and clinical information from the clinical systems.
- Entering information into the appropriate EMR and eCRF systems and departmental systems in an accurate manner.
- Reviewing data for quality and completeness based on established queries.
- Assists with the coordination of the collection, processing, organization, and storage of biological specimens in the systems
- May be responsible for IRB and regulatory submissions and maintenance of regulatory files
- Maintaining on-going communications with research managers and PIs for data collection needs.
- Bachelor’s Degree required
- 2-5 years of experience in a research setting
- Special Intermittent Project Responsibilities (2-5/year)
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