Clinical Research Coordinator
When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives.
Job Type:
RegularScheduled Hours:
40Work Shift:
Day (United States of America)Assists in the setup, monitoring, and completion of clinical research trials undertaken by the Principal Investigator in accordance with NEBH policies and procedures and Federal regulations.
The position works directly with patients, staff and physicians at the hospital to coordinate study logistics.
Duties include participant identification, recruitment, eligibility screening, appointment scheduling, direct patient interactions, survey administration, data collection, and other administrative duties as needed in support of the study.
Working with a research team and hospital staff that is available to mentor, answer questions and conduct required trainings.
This position is perfect for those looking to gain 1-2 years of experience in clinical settings before moving on to other professions.
Permanent job seeker welcomed as well.
Job Description:
SummaryAssists in the setup, monitoring, and completion of clinical research trials undertaken by the Principal Investigator in accordance with NEBH policies and procedures and Federal regulations.
The position works directly with patients, staff and physicians at the hospital to coordinate study logistics.
Duties include participant identification, recruitment, eligibility screening, appointment scheduling, direct patient interactions, survey administration, data collection, and other administrative duties as needed in support of the study.
Working with a research team and hospital staff that is available to mentor, answer questions and conduct required trainings.
This position is perfect for those looking to gain 1-2 years of experience in clinical settings before moving on to other professions.
Permanent job seeker welcomed as well.
Primary Duties and
Responsibilities:
Coordinates subject visits and follow-up appointments, administers surveys to subjects, attends study meetings, reports study progress, tracks subject data and specimen collection and delivery, and implements recruitment and retention strategies Prepares regulatory documents according to FDA standards when necessary Maintains subject records and documentation according to HIPAA, GCP and sponsor requirements Completes and submits Institutional Review Board (IRB) research documents with assistance Documents and maintains study procedures according to Good Clinical Practice (GCP) and Standard Operating Procedures; ensures compliance with protocol, and maintains appropriate procedures for documenting protocol deviations and adverse events Review medical records and extract data from hospital databases for purposes of specific studies Provide administrative support on REDCap and Patient IQ to researchers Facilitate submission of scientific deliverables (journal article manuscript and conference abstract) Correspond with researchers to monitor study progress Schedule, participate, and take minutes in meetings with researchers Perform data analysis as needed Support office administrative tasks as needed Assist with writing study manuscript, depending on candidate's capacity Key Competencies:
BS/BA in pre-med, biostatistics, or other health-related field required Good Clinical Practice (GCP) and research ethics certificates a plus, or obtain within two weeks of hire Proficiency in MS Excel and data management a plus Strong interests in clinical research Customer service focused with ability to listen and work with multiple levels of individuals within the hospital Adept at keeping regulatory material and notes neat, organized and complete; responsible for tracking necessary industry information Able to communicate study updates, patient recruitment status and logistical processes clearly to physicians, staff and manager Accountable of time and able to understand surgery schedules Comfortable working with a department of 4-5 individuals but having access to the entire hospital staff and physicians Professional Opportunities for the Candidates:
Opportunities to work closely with surgeons in a top tier orthopaedic program Clinical exposure to orthopaedic surgery Opportunities to co-author publications Experience with all facets of clinical research, including study conceptualization, human subject protection, data gathering and analysis, manuscript preparation and submission FLSA Status:
ExemptAs a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities.
Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) and COVID-19 as a condition of employment.
Learn more about this requirement.
More than 35,000 people working together.
Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives.
Your skill and compassion can make us even stronger.
Equal Opportunity Employer/Veterans/Disabled Recommended Skills Active Listening Administration Clinical Research Clinical Works Data Analysis Data Collection Estimated Salary: $20 to $28 per hour based on qualifications.
Job Type:
RegularScheduled Hours:
40Work Shift:
Day (United States of America)Assists in the setup, monitoring, and completion of clinical research trials undertaken by the Principal Investigator in accordance with NEBH policies and procedures and Federal regulations.
The position works directly with patients, staff and physicians at the hospital to coordinate study logistics.
Duties include participant identification, recruitment, eligibility screening, appointment scheduling, direct patient interactions, survey administration, data collection, and other administrative duties as needed in support of the study.
Working with a research team and hospital staff that is available to mentor, answer questions and conduct required trainings.
This position is perfect for those looking to gain 1-2 years of experience in clinical settings before moving on to other professions.
Permanent job seeker welcomed as well.
Job Description:
SummaryAssists in the setup, monitoring, and completion of clinical research trials undertaken by the Principal Investigator in accordance with NEBH policies and procedures and Federal regulations.
The position works directly with patients, staff and physicians at the hospital to coordinate study logistics.
Duties include participant identification, recruitment, eligibility screening, appointment scheduling, direct patient interactions, survey administration, data collection, and other administrative duties as needed in support of the study.
Working with a research team and hospital staff that is available to mentor, answer questions and conduct required trainings.
This position is perfect for those looking to gain 1-2 years of experience in clinical settings before moving on to other professions.
Permanent job seeker welcomed as well.
Primary Duties and
Responsibilities:
Coordinates subject visits and follow-up appointments, administers surveys to subjects, attends study meetings, reports study progress, tracks subject data and specimen collection and delivery, and implements recruitment and retention strategies Prepares regulatory documents according to FDA standards when necessary Maintains subject records and documentation according to HIPAA, GCP and sponsor requirements Completes and submits Institutional Review Board (IRB) research documents with assistance Documents and maintains study procedures according to Good Clinical Practice (GCP) and Standard Operating Procedures; ensures compliance with protocol, and maintains appropriate procedures for documenting protocol deviations and adverse events Review medical records and extract data from hospital databases for purposes of specific studies Provide administrative support on REDCap and Patient IQ to researchers Facilitate submission of scientific deliverables (journal article manuscript and conference abstract) Correspond with researchers to monitor study progress Schedule, participate, and take minutes in meetings with researchers Perform data analysis as needed Support office administrative tasks as needed Assist with writing study manuscript, depending on candidate's capacity Key Competencies:
BS/BA in pre-med, biostatistics, or other health-related field required Good Clinical Practice (GCP) and research ethics certificates a plus, or obtain within two weeks of hire Proficiency in MS Excel and data management a plus Strong interests in clinical research Customer service focused with ability to listen and work with multiple levels of individuals within the hospital Adept at keeping regulatory material and notes neat, organized and complete; responsible for tracking necessary industry information Able to communicate study updates, patient recruitment status and logistical processes clearly to physicians, staff and manager Accountable of time and able to understand surgery schedules Comfortable working with a department of 4-5 individuals but having access to the entire hospital staff and physicians Professional Opportunities for the Candidates:
Opportunities to work closely with surgeons in a top tier orthopaedic program Clinical exposure to orthopaedic surgery Opportunities to co-author publications Experience with all facets of clinical research, including study conceptualization, human subject protection, data gathering and analysis, manuscript preparation and submission FLSA Status:
ExemptAs a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities.
Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) and COVID-19 as a condition of employment.
Learn more about this requirement.
More than 35,000 people working together.
Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives.
Your skill and compassion can make us even stronger.
Equal Opportunity Employer/Veterans/Disabled Recommended Skills Active Listening Administration Clinical Research Clinical Works Data Analysis Data Collection Estimated Salary: $20 to $28 per hour based on qualifications.
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