PRN Registered Nurse (Night Shifts - 530 pm – 6 am)
for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we can have headings like About Us? Not listed but we can still use for any section heading. The posting includes "About Us" paragraph, "Job Summary", "Job Summary", "Essential Responsibilities And Duties", "Education/Experience/Skills", "Working Conditions". Also maybe "Benefits", "Pay", "Schedule" not present. So we should only include sections that have real content.
We need to preserve all substantive info, not repeat job title, not include Job ID etc. Remove boilerplate: EEO line at end should be removed. Also maybe "CenExel Clinical Research is an Equal Opportunity Employer..." remove.
We need to format lists with - for any list of duties/requirements/benefits. So for responsibilities list, we need to turn each bullet into
- . The responsibilities are currently a paragraph with semicolons and commas. We need to split into list items. The instruction: "Use
- for any list of duties/requirements/benefits". So we should create a list for responsibilities. Also for Education/Experience/Skills we can list each requirement as
- . Also maybe Working Conditions as
or list? It's prose; we can keep as
.
We must not invent or summarize away detail. Must preserve all substantive information. So we need to capture each responsibility point.
Let's extract responsibilities from the text:
"Essential Responsibilities And Duties Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.Reviews and executes clinical research protocols.Completes and maintains study documents in accordance with sponsor and site requirements.Possible recruitment of potential study subjects.Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.Maintains adequate inventory of all data and supplies.Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.Observes, documents, reports, and follows up on adverse events and serious adverse events.Conducts the informed consent process, per CenExel Standard Operating Procedures.Follows up appropriately on all laboratory results.Maintains safety standards when performing job responsibilities.Maintains study logs and site relationsEnsures proper collection, processing, and shipment (if applicable) of laboratory specimens.Assists with quality assurance activities and completes queries, as applicable.Obtains Principal Investigator signatures on necessary documents.Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol.Ensures accountability and adequate supply for study and clinical drugs.Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.Assumes other duties and responsibilities as assigned."
We need to split each sentence or clause separated by periods. Let's list them:
1. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
2. Reviews and executes clinical research protocols.
3. Completes and maintains study documents in accordance with sponsor and site requirements.
4. Possible recruitment of potential study subjects.
5. Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
6. Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
7. Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
8. Maintains adequate inventory of all data and supplies.
9. Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
10. Observes, documents, reports, and follows up on adverse events and serious adverse events.
11. Conducts the informed consent process, per CenExel Standard Operating Procedures.
12. Follows up appropriately on all laboratory results.
13. Maintains safety standards when performing job responsibilities.
14. Maintains study logs and site relations
15. Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens.
16. Assists with quality assurance activities and completes queries, as applicable.
17. Obtains Principal Investigator signatures on necessary documents.
18. Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol.
19. Ensures accountability and adequate supply for study and clinical drugs.
20. Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
21. Assumes other duties and responsibilities as assigned.
Note: Some items may be combined; but we can keep as separate
- .
Now Education/Experience/Skills list:
"Must be a Registered Nurse with a current license in Florida, and not have any disciplinary action on the license.
Must be BLS or ACLS certified or able to obtain.
0-1 year of experience is required.
Must be IV certified, depending on site.
Must be capable of performing all clinical tasks relevant to licensure and/or training.
Must be able to clearly communicate verbally with patients.
Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
Must be self-motivated and able to perform tasks independently.
Ability to react calmly and effectively in emergency situations.
Must reflect the professional image of the company, upholding the company vision in actions and demeanor.
Must be able to effectively communicate verbally and in writing.
Must be able to work night Shift – 5:30 pm to 6 am (potential for an occasional day shift but the focus is the night shift)
Bilingual (English - Spanish) - preferred
Clinical Research background a plus"
We need to list each as
- . Also note "0-1 year of experience is required." Keep.
Now Working Conditions paragraph: "Indoor, Clinic environment.Essential physical requirements include sitting, typing, standing, and walking.Lightly active position, occasional lifting of up to 20 pounds.Reporting to work, as scheduled, is essential.On-site work arrangement."
We can keep as
maybe with sentences separated by periods.
Now About Us paragraph: "Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success."
We can put as
under heading About Us.
Job Summary paragraph: "With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process."
We can put as
under heading Job Summary.
Now we need to output HTML fragment only, no /. Use
for each section heading.
We should not repeat job title as heading. The job title is Clinical Research RN I? Not needed.
We should not include Job ID etc.
We should not include EEO line.
We should not include any filler like "commensurate with experience". Not present.
Now produce HTML:
About Us
Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Job Summary
With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process.
Responsibilities
- Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
- Reviews and executes clinical research protocols.
- Completes and maintains study documents in accordance with sponsor and site requirements.
- Possible recruitment of potential study subjects.
- Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
- Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
- Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
- Maintains adequate inventory of all data and supplies.
- Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
- Observes, documents, reports, and follows up on adverse events and serious adverse events.
- Conducts the informed consent process, per CenExel Standard Operating Procedures.
- Follows up appropriately on all laboratory results.
- Maintains safety standards when performing job responsibilities.
- Maintains study logs and site relations
- Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens.
- Assists with quality assurance activities and completes queries, as applicable.
- Obtains Principal Investigator signatures on necessary documents.
- Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol.
- Ensures accountability and adequate supply for study and clinical drugs.
- Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
- Assumes other duties and responsibilities as assigned.
Education/Experience/Skills
- Must be a Registered Nurse with a current license in Florida, and not have any disciplinary action on the license.
- Must be BLS or ACLS certified or able to obtain.
- 0-1 year of experience is required.
- Must be IV certified, depending on site.
- Must be capable of performing all clinical tasks relevant to licensure and/or training.
- Must be able to clearly communicate verbally with patients.
- Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
- Must be self-motivated and able to perform tasks independently.
- Ability to react calmly and effectively in emergency situations.
- Must reflect
- for any list of duties/requirements/benefits. So for responsibilities list, we need to turn each bullet into
- . The responsibilities are currently a paragraph with semicolons and commas. We need to split into list items. The instruction: "Use
- for any list of duties/requirements/benefits". So we should create a list for responsibilities. Also for Education/Experience/Skills we can list each requirement as
- . Also maybe Working Conditions as
or list? It's prose; we can keep as
. We must not invent or summarize away detail. Must preserve all substantive information. So we need to capture each responsibility point. Let's extract responsibilities from the text: "Essential Responsibilities And Duties Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.Reviews and executes clinical research protocols.Completes and maintains study documents in accordance with sponsor and site requirements.Possible recruitment of potential study subjects.Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.Maintains adequate inventory of all data and supplies.Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.Observes, documents, reports, and follows up on adverse events and serious adverse events.Conducts the informed consent process, per CenExel Standard Operating Procedures.Follows up appropriately on all laboratory results.Maintains safety standards when performing job responsibilities.Maintains study logs and site relationsEnsures proper collection, processing, and shipment (if applicable) of laboratory specimens.Assists with quality assurance activities and completes queries, as applicable.Obtains Principal Investigator signatures on necessary documents.Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol.Ensures accountability and adequate supply for study and clinical drugs.Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.Assumes other duties and responsibilities as assigned." We need to split each sentence or clause separated by periods. Let's list them: 1. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. 2. Reviews and executes clinical research protocols. 3. Completes and maintains study documents in accordance with sponsor and site requirements. 4. Possible recruitment of potential study subjects. 5. Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log. 6. Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol. 7. Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor. 8. Maintains adequate inventory of all data and supplies. 9. Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned. 10. Observes, documents, reports, and follows up on adverse events and serious adverse events. 11. Conducts the informed consent process, per CenExel Standard Operating Procedures. 12. Follows up appropriately on all laboratory results. 13. Maintains safety standards when performing job responsibilities. 14. Maintains study logs and site relations 15. Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens. 16. Assists with quality assurance activities and completes queries, as applicable. 17. Obtains Principal Investigator signatures on necessary documents. 18. Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol. 19. Ensures accountability and adequate supply for study and clinical drugs. 20. Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies. 21. Assumes other duties and responsibilities as assigned. Note: Some items may be combined; but we can keep as separate
- . Now Education/Experience/Skills list: "Must be a Registered Nurse with a current license in Florida, and not have any disciplinary action on the license. Must be BLS or ACLS certified or able to obtain. 0-1 year of experience is required. Must be IV certified, depending on site. Must be capable of performing all clinical tasks relevant to licensure and/or training. Must be able to clearly communicate verbally with patients. Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc. Must be self-motivated and able to perform tasks independently. Ability to react calmly and effectively in emergency situations. Must reflect the professional image of the company, upholding the company vision in actions and demeanor. Must be able to effectively communicate verbally and in writing. Must be able to work night Shift – 5:30 pm to 6 am (potential for an occasional day shift but the focus is the night shift) Bilingual (English - Spanish) - preferred Clinical Research background a plus" We need to list each as
- . Also note "0-1 year of experience is required." Keep.
Now Working Conditions paragraph: "Indoor, Clinic environment.Essential physical requirements include sitting, typing, standing, and walking.Lightly active position, occasional lifting of up to 20 pounds.Reporting to work, as scheduled, is essential.On-site work arrangement."
We can keep as
maybe with sentences separated by periods. Now About Us paragraph: "Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success." We can put as
under heading About Us. Job Summary paragraph: "With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process." We can put as
under heading Job Summary. Now we need to output HTML fragment only, no /. Use
for each section heading. We should not repeat job title as heading. The job title is Clinical Research RN I? Not needed. We should not include Job ID etc. We should not include EEO line. We should not include any filler like "commensurate with experience". Not present. Now produce HTML:
About Us
Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Job Summary
With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process.
Responsibilities
- Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
- Reviews and executes clinical research protocols.
- Completes and maintains study documents in accordance with sponsor and site requirements.
- Possible recruitment of potential study subjects.
- Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
- Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
- Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
- Maintains adequate inventory of all data and supplies.
- Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
- Observes, documents, reports, and follows up on adverse events and serious adverse events.
- Conducts the informed consent process, per CenExel Standard Operating Procedures.
- Follows up appropriately on all laboratory results.
- Maintains safety standards when performing job responsibilities.
- Maintains study logs and site relations
- Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens.
- Assists with quality assurance activities and completes queries, as applicable.
- Obtains Principal Investigator signatures on necessary documents.
- Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol.
- Ensures accountability and adequate supply for study and clinical drugs.
- Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
- Assumes other duties and responsibilities as assigned.
Education/Experience/Skills
- Must be a Registered Nurse with a current license in Florida, and not have any disciplinary action on the license.
- Must be BLS or ACLS certified or able to obtain.
- 0-1 year of experience is required.
- Must be IV certified, depending on site.
- Must be capable of performing all clinical tasks relevant to licensure and/or training.
- Must be able to clearly communicate verbally with patients.
- Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
- Must be self-motivated and able to perform tasks independently.
- Ability to react calmly and effectively in emergency situations.
- Must reflect