Senior Clinical Research Coordinator

Integrated Resources, Inc ( IRI ) provided pay range

This range is provided by Integrated Resources, Inc ( IRI ). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$32.00/hr - $35.00/hr

Direct message the job poster from Integrated Resources, Inc ( IRI )

Lead Recruiter at Integrated Resources Inc.(Scientific/ Clinical/Life Sciences /Pharmaceuticals /Engineering/Healthcare/ Business Professionals)

Title:
Clinical Research Coordinator II, Cancer

Duration: 4+ months

Shift: Flexibility to start at 7 am if visits start early, 8 hours per day, M-F

Job Description:

• 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 medical records for patients, including review of pathology reports.
• Accessing patient demographic and clinical information from the clinical systems.
• Enter 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 system.
• 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.
• Must have computer skills including the use of Microsoft Office Suite.

Requirements:

• Bachelor’s Degree is required.
• 2-5 years of experience in a research setting.
• 2 years' experience, preferably operating as a CRC II;
  Preference with interventional trials.
• Experience with hematology/Amyloid/cancer trials.
• Sickle Cell Project.

Seniority level

• Seniority level Associate

Employment type

• Employment type
  
  Contract

Job function

• Job function
  
  Science, Research, and Other
• Industries Hospitals and Health Care, Hospitals, and Health and Human Services

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