NP/PA — BOTOX® Injector (New York)
for section headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We must not repeat job title as heading. We need to include sections only when posting has real specific content. We have content for: About the role (maybe the introductory paragraph about Adams Clinical and mission). Could be "About the role" or "About the organization". The instruction says use headings e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. So we should map content accordingly.
We have:
- Intro paragraph about Adams Clinical: mission, vision, values, culture. That could be "About the role"? Actually "About the role" would be description of the role. But we have a separate "Job Role" section describing the position focus. So we could treat the initial paragraph as "About the role" or maybe "About the organization". But we must stick to allowed headings. Probably "About the role" can include the description of the organization and role context. Then we have "Responsibilities" from Key Responsibilities. Then "Requirements" from Job Requirements (including education, licensure, experience). Then "Qualifications" maybe overlapping with Requirements; but we can combine or separate. The instruction says prefer a few substantive sections over many thin ones. So we could have About the role, Responsibilities, Requirements, Benefits, Pay. Schedule is mentioned: "This is a per diem position, with hours scheduled based on study and clinical needs. Candidates must have the availability to provide on-site clinical support at least 2 weekdays per week..." That's schedule info. So we can include Schedule section.
We must not include sections with filler like "commensurate with experience" for Pay? Actually Pay is given: "$85-95 per hour commensurate with experience". That's specific enough; we can include Pay section with that sentence. Benefits: "401(k) / 401(k) matching". That's specific. So include Benefits.
We must remove boilerplate: EEO, legal, etc. Also remove duplicated lines. Also remove application instructions (none present). Also remove cookie/navigation etc.
We must preserve all substantive information. So we need to include all duties, requirements, etc.
We need to format lists with - . For prose use
.
We must not repeat job title as heading. The job title is "Per Diem Nurse Practitioner (NP) or Physician Assistant (PA)". We must not put that as heading.
We must not put Job ID/requisition numbers as headings (none present).
We need to output only HTML fragment, no /, no markdown fences.
Let's extract content.
Intro paragraph (first block):
"Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change. At Adams Clinical, you’ll find: A culture of respect, transparency, and continuous improvementOpportunities for professional growth and learningA team dedicated to improving lives through innovation and integrity If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team."
We need to format that as prose
. Possibly break into sentences but can be one
.
Then "Job Role This position is focused primarily on administering BOTOX® injections in support of a chronic migraine clinical trial, alongside other clinical support duties as outlined below. Adams Clinical is seeking a Per Diem Nurse Practitioner (NP) or Physician Assistant (PA) to provide flexible, as-needed clinical support at our New York City locations. This role works under the supervision of our physician Principal Investigators and Clinical Operations leadership on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines. Typical tasks will include, but are not limited to, IV catheterization and drug infusion, injections, phlebotomy, medical record and clinical results review, medication reconciliation, and medical liaising. The ideal candidate will have recent injection experience and must be comfortable working in a clinical research environment, following study protocols, and maintaining clear and timely documentation in accordance with study protocols and applicable research and regulatory requirements."
That could be part of About the role or separate. Since we have About the role heading, we can combine intro and Job Role into About the role.
Then Responsibilities: list from Key Responsibilities. Let's extract each bullet:
- Availability to provide on-site clinical support at least 2 weekdays per week, as needed to support protocol-required activities and participant visits. The expected frequency of availability may be adjusted based on applicable study protocols, site needs, and operational requirements.
- IV placement, initiation and monitoring of IV infusions in accordance with the study protocol
- Administer subcutaneous and intramuscular injections in accordance with study protocols
- Support the preparation and handling of investigational product, as needed and as permitted by the study protocol, site procedures, and applicable requirements
- Perform physical exams and other protocol-required assessments within scope of practice
- Perform clinical review and assessment of protocol-required results and clinical data (e.g., laboratory results, ECGs, and vital signs) in collaboration with site Principal Investigators
- Identify and escalate clinically significant findings, changes in participant condition, and potential reactions to study dosing, including those that may impact participant safety or subsequent dosing, in collaboration with the site Principal Investigators
- Assist with difficult phlebotomy and IV placement for blood collection, as needed
- Review medical records and reconcile relevant information with patient-reported history
- Assist with collection and documentation of adverse events (AEs), concomitant medications, medical history
- Assist with identification, documentation, and reporting of Serious Adverse Events (SAEs), including required regulatory/IRB documentation
- Provide on-site clinical support during emergency situations, as needed
- Document clinical assessments, procedures, and participant-related information accurately and in a timely manner in accordance with study protocols and applicable requirements.
We need to put each as
- . Some are long sentences; okay.
Then Requirements: from Job Requirements.
List:
- BOTOX® injection experience required
- Bachelor’s degree and advanced clinical degree appropriate to Nurse Practitioner or Physician Assistant practice required
- Current, unrestricted New York RN license and New York CRNP certification, with current national certification in the applicable NP specialty; OR current, unrestricted New York PA license and registration and NCCPA certification (PA-C) as a Physician Assistant required
- 2+ years of experience as an NP or PA preferred
- Injection Experience (Required): At least 1 year of experience administering BOTOX® or other neurotoxin injections, with a minimum of 2 patients treated or 8 treatment sessions completed
- Other relevant injection experience (e.g., dermatology or aesthetic injections) will also be considered, subject to Sponsor review
- Experience administering BOTOX® specifically for chronic migraine is a plus — but not required to apply
- BLS/CPR certification preferred
- Previous clinical research experience preferred, but not required
- Strong attention to detail and ability to follow study protocols and established clinical procedures while maintaining clear, accurate, and timely clinical documentation
- This is a per diem position, with hours scheduled based on study and clinical needs. Candidates must have the availability to provide on-site clinical support at least 2 weekdays per week, as needed to support protocol-required activities and participant visits. The expected frequency of availability may be adjusted based on applicable study protocols, site needs, and operational requirements.
Note the last bullet duplicates availability from responsibilities; but we can keep it in Requirements or maybe move to Schedule. We'll handle Schedule separately.
We need to avoid duplication; but instruction says preserve ALL substantive information; we can keep duplicate but maybe better to not duplicate. However we must not invent or summarize away detail. Duplication is okay if it's in original; but we could keep it only once. However the duplicate is exactly same sentence as in Responsibilities first bullet. To preserve all info, we could keep it in Responsibilities and not repeat in Requirements. But the Requirements section includes that sentence as part of the list; if we omit it, we are removing substantive information (the sentence). However it's already present in Responsibilities; but the requirement is about availability; it's still substantive. If we keep it only in Responsibilities, we still have the info. The instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." If we keep it only once, we still preserve the information (not removed). It's not summarizing away; it's just not duplicated. I think it's acceptable to avoid duplication. But to be safe, we could include it in both sections; duplication is not prohibited. However they said "remove duplicated lines". That refers to boilerplate/duplicated lines in the posting. The duplicate availability line is duplicated in the posting; we should remove duplicated lines. So we should keep only one instance. So we will keep it in Responsibilities (or Schedule) and not repeat in Requirements.
Thus Requirements list will exclude that duplicate line.
Now Benefits: "401(k) / 401(k) matching". That's it.
Pay: "$85-95 per hour commensurate with experience". That's specific.
Schedule: we have info about per diem, hours scheduled based on study and clinical needs, availability at least 2 weekdays per week, etc. We'll put that in Schedule section.
We must not create Pay/Schedule/Benefits sections unless posting actually states them. They do.
Now we need to decide headings: About the role, Responsibilities, Requirements, Benefits, Pay, Schedule. Possibly also Qualifications? But we have Requirements covering qualifications; we can skip Qualifications to avoid thin sections. The instruction: Prefer a few substantive sections over many thin ones. So we can omit Qualifications.
Now we need to output HTML fragment.
Structure:
About the role
... combined intro + Job Role ...
Responsibilities
- ... each bullet ...
Requirements
- ... each bullet except duplicate availability ...
Benefits
401(k) / 401(k) matching
Pay
$85-95 per hour commensurate with experience
Schedule
This is a per diem position, with hours scheduled based on study and clinical needs. Candidates must have the availability to provide on-site clinical support at least 2 weekdays per week, as needed to support protocol-required activities and participant visits. The expected frequency of availability may be adjusted based on applicable study protocols, site needs, and operational requirements.
We need to ensure we didn't include any boilerplate like EEO etc. Also remove lines like "Adams Clinical is committed to being an equal opportunity and affirmative action employer..." etc. Also remove "In compliance with federal law..." etc.
Now we need to craft the About the role paragraph.
Combine:
"Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and
. We must not repeat job title as heading. The job title is "Per Diem Nurse Practitioner (NP) or Physician Assistant (PA)". We must not put that as heading. We must not put Job ID/requisition numbers as headings (none present). We need to output only HTML fragment, no /, no markdown fences. Let's extract content. Intro paragraph (first block): "Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change. At Adams Clinical, you’ll find: A culture of respect, transparency, and continuous improvementOpportunities for professional growth and learningA team dedicated to improving lives through innovation and integrity If you’re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we’d love to have you on our team." We need to format that as prose
. Possibly break into sentences but can be one
. Then "Job Role This position is focused primarily on administering BOTOX® injections in support of a chronic migraine clinical trial, alongside other clinical support duties as outlined below. Adams Clinical is seeking a Per Diem Nurse Practitioner (NP) or Physician Assistant (PA) to provide flexible, as-needed clinical support at our New York City locations. This role works under the supervision of our physician Principal Investigators and Clinical Operations leadership on the conduct of pharmaceutical-sponsored clinical trials in accordance with FDA regulations and GCP guidelines. Typical tasks will include, but are not limited to, IV catheterization and drug infusion, injections, phlebotomy, medical record and clinical results review, medication reconciliation, and medical liaising. The ideal candidate will have recent injection experience and must be comfortable working in a clinical research environment, following study protocols, and maintaining clear and timely documentation in accordance with study protocols and applicable research and regulatory requirements." That could be part of About the role or separate. Since we have About the role heading, we can combine intro and Job Role into About the role. Then Responsibilities: list from Key Responsibilities. Let's extract each bullet: - Availability to provide on-site clinical support at least 2 weekdays per week, as needed to support protocol-required activities and participant visits. The expected frequency of availability may be adjusted based on applicable study protocols, site needs, and operational requirements. - IV placement, initiation and monitoring of IV infusions in accordance with the study protocol - Administer subcutaneous and intramuscular injections in accordance with study protocols - Support the preparation and handling of investigational product, as needed and as permitted by the study protocol, site procedures, and applicable requirements - Perform physical exams and other protocol-required assessments within scope of practice - Perform clinical review and assessment of protocol-required results and clinical data (e.g., laboratory results, ECGs, and vital signs) in collaboration with site Principal Investigators - Identify and escalate clinically significant findings, changes in participant condition, and potential reactions to study dosing, including those that may impact participant safety or subsequent dosing, in collaboration with the site Principal Investigators - Assist with difficult phlebotomy and IV placement for blood collection, as needed - Review medical records and reconcile relevant information with patient-reported history - Assist with collection and documentation of adverse events (AEs), concomitant medications, medical history - Assist with identification, documentation, and reporting of Serious Adverse Events (SAEs), including required regulatory/IRB documentation - Provide on-site clinical support during emergency situations, as needed - Document clinical assessments, procedures, and participant-related information accurately and in a timely manner in accordance with study protocols and applicable requirements. We need to put each as
About the role
... combined intro + Job Role ...
Responsibilities
- ... each bullet ...
Requirements
- ... each bullet except duplicate availability ...
Benefits
401(k) / 401(k) matching
Pay
$85-95 per hour commensurate with experience
Schedule
This is a per diem position, with hours scheduled based on study and clinical needs. Candidates must have the availability to provide on-site clinical support at least 2 weekdays per week, as needed to support protocol-required activities and participant visits. The expected frequency of availability may be adjusted based on applicable study protocols, site needs, and operational requirements.
We need to ensure we didn't include any boilerplate like EEO etc. Also remove lines like "Adams Clinical is committed to being an equal opportunity and affirmative action employer..." etc. Also remove "In compliance with federal law..." etc. Now we need to craft the About the role paragraph. Combine: "Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and