ICONMA
Overview
Our Client, a Medical Center company, is looking for a Clinical Research Coordinator for their Boston, MA/ Hybrid location.
Responsibilities
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 ongoing communications with research managers and PIs for data collection needs.
Qualifications
Excellent organization and communications skills required.
Strong interpersonal skills; ability to effectively interact with all levels of staff and external contacts.
Must be detail oriented and have the ability to follow-through.
Ability to effectively manage time and prioritize workload.
Must practice discretion and adhere to hospital confidentiality guidelines at all times.
Must have computer skills including the use of Microsoft Office Suite.
Bachelor’s Degree required.
2-5 years of experience in a research setting.
Special Intermittent Project Responsibilities (2-5/year).
Master’s degree.
Why Should You Apply?
Health Benefits
Referral Program
Excellent growth and advancement opportunities
As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or expression, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.
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Responsibilities
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 ongoing communications with research managers and PIs for data collection needs.
Qualifications
Excellent organization and communications skills required.
Strong interpersonal skills; ability to effectively interact with all levels of staff and external contacts.
Must be detail oriented and have the ability to follow-through.
Ability to effectively manage time and prioritize workload.
Must practice discretion and adhere to hospital confidentiality guidelines at all times.
Must have computer skills including the use of Microsoft Office Suite.
Bachelor’s Degree required.
2-5 years of experience in a research setting.
Special Intermittent Project Responsibilities (2-5/year).
Master’s degree.
Why Should You Apply?
Health Benefits
Referral Program
Excellent growth and advancement opportunities
As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or expression, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.
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