Senior Clinical Research Coordinator

Integrated Resources, Inc ( IRI )

Boston (MA)

On-site

USD 67,000 - 73,000

Full time

14 days+

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Job summary

Integrated Resources, Inc (IRI) is seeking a Clinical Research Coordinator II specializing in cancer studies for a contract position. You will conduct essential research activities under supervision, including patient recruitment and data management, contributing to groundbreaking trials in a supportive clinical environment. The ideal candidate will hold a Bachelor’s Degree with 2-5 years of related experience, particularly in hematology and cancer research.

Qualifications

Requires a Bachelor’s Degree.
2-5 years of experience in a research setting specifically as a Clinical Research Coordinator.
Experience with hematology/Amyloid/cancer trials preferred.

Responsibilities

Perform research activities and maintain patient databases.
Conduct patient recruitment and data entry into electronic systems.
Assist with audits and quality improvement projects.

Skills

Data Entry

Patient Recruitment

Quality Improvement

Computer Skills

Education

Bachelor’s Degree

Tools

Microsoft Office Suite

Job description

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