| Classification Title: | Clinical Research Coordinator III -Division of Pulmonary Critical Care & Sleep Medicine |
|---|
| Classification Minimum Requirements: | Bachelors degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience. |
|---|
| Job Description: | Clinical Trial Project Management
Support the principal investigator with industry-sponsored clinical trials or internally funded clinical research. Screen daily/weekly to enroll patients into clinical trials. Coordinate with the Clinical Research Center inpatient unit or inpatient auxiliaries to schedule patients for study visits. Visit the study and monitor regularly to ensure compliance with industry protocols. Ensure compliance with the Divisional research tracking log. Process patient stipends. Assist the Division Administrator with any internal/external audits. Attend industry-sponsored investigator meetings to gather updates on protocol changes upcoming amendments and related items. Respond to any new industry-sponsored solicitations. Regularly review research study billing to ensure compliance.
Clinical trial regulatory management
Prepare all RAC paperwork needed for study startup approval. Prepare IRB paperwork needed for study startup. Obtain RAC or IRB approval for amendments protocol changes and related activities. Assist with registration of the study in database. Comply with all institutional federal state sponsor and Divisional policies. Retain records/archive documents after study close-out
Clinical Trials budget
Assist the Division Administrator with the industry-sponsored budget proposal. Obtain the cost of services for all procedures study visits etc. related to the trial. Work with the Division Administrator to assess the studys financial feasibility.
This position will perform ad hoc assignments as assigned by the Supervisor |
|---|
| Expected Salary: | $53000 - $66900/annually |
|---|
| Required Qualifications: | Bachelors degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience. |
|---|
| Preferred: | Masters degree and five years of relevant Pulmonary clinical trial experience. Prefer experience and/or certification in Spirometry. |
|---|
| Special Instructions to Applicants: | Application must be submitted by 11:55 p.m. (ET) of the posting end date. |
|---|
| Health Assessment Required: | Yes |
|---|
Required Experience:
IC
Classification Title:Clinical Research Coordinator III -Division of Pulmonary Critical Care & Sleep MedicineClassification Minimum Requirements:Bachelors degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience.Job Description:Cli...
| Classification Title: | Clinical Research Coordinator III -Division of Pulmonary Critical Care & Sleep Medicine |
|---|
| Classification Minimum Requirements: | Bachelors degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience. |
|---|
| Job Description: | Clinical Trial Project Management
Support the principal investigator with industry-sponsored clinical trials or internally funded clinical research. Screen daily/weekly to enroll patients into clinical trials. Coordinate with the Clinical Research Center inpatient unit or inpatient auxiliaries to schedule patients for study visits. Visit the study and monitor regularly to ensure compliance with industry protocols. Ensure compliance with the Divisional research tracking log. Process patient stipends. Assist the Division Administrator with any internal/external audits. Attend industry-sponsored investigator meetings to gather updates on protocol changes upcoming amendments and related items. Respond to any new industry-sponsored solicitations. Regularly review research study billing to ensure compliance.
Clinical trial regulatory management
Prepare all RAC paperwork needed for study startup approval. Prepare IRB paperwork needed for study startup. Obtain RAC or IRB approval for amendments protocol changes and related activities. Assist with registration of the study in database. Comply with all institutional federal state sponsor and Divisional policies. Retain records/archive documents after study close-out
Clinical Trials budget
Assist the Division Administrator with the industry-sponsored budget proposal. Obtain the cost of services for all procedures study visits etc. related to the trial. Work with the Division Administrator to assess the studys financial feasibility.
This position will perform ad hoc assignments as assigned by the Supervisor |
|---|
| Expected Salary: | $53000 - $66900/annually |
|---|
| Required Qualifications: | Bachelors degree in an appropriate area and three years of relevant experience; or an equivalent combination of education and experience. |
|---|
| Preferred: | Masters degree and five years of relevant Pulmonary clinical trial experience. Prefer experience and/or certification in Spirometry. |
|---|
| Special Instructions to Applicants: | Application must be submitted by 11:55 p.m. (ET) of the posting end date. |
|---|
| Health Assessment Required: | Yes |
|---|
Required Experience:
IC
View more
View less
Job Location:
Monthly Salary:
Not Disclosed
Posted on:
7 hours ago
Vacancies:
1 Vacancy
