Senior Clinical Lab Research Specialist - Onsite (Urgent Need)

We need to output HTML fragment with sections: About the role? The posting includes Job Summary, Primary Duties..., Knowledge And Skills, Education And Experience. Also includes location, duration, hours, shift, client, job category, employment type, onsite rate, panel drug test required, etc. According to rules: we should not repeat job title as heading. We should not put Job ID etc. We should include sections only when posting has real specific content. We need to include sections like About the role (maybe Job Summary), Responsibilities (Primary Duties...), Requirements (Knowledge And Skills, Education And Experience), maybe Benefits? Not present. Pay? It says Onsite Rate: $60/hr. That's pay info, so we should include a Pay section. Schedule? It says Total Hours/week: 40.00, 1st Shift. That's schedule info, so include Schedule section. Benefits? Not mentioned. So we can include Pay and Schedule sections. We also need to include location maybe in a short paragraph? The rule says minor metadata can be folded into a short

or drop it. So we can include a paragraph with location, duration, hours, shift, client, job category, employment type, etc. Or we can embed those in a short

. We'll not create headings for them. We must not include boilerplate like EEO etc. There's none. We need to preserve all substantive info: include BS ASCP MT/MLT CLS Certification check if active, 5 years experience, calibration of equipment, generate date, read data, analysis, phlebotomy experience a plus, follow protocol, sample handling add instrument experience see list below, Hepatitis Vaccine required, etc. Also mention "Panel drug test required". Also "Onsite Rate: $60/hr". Also "Total Hours/week: 40.00". Also "1st Shift". Also "Duration: 12 Months". Also "Location: Franklin Lakes, NJ". Also "Client: Medical Devices Company". Also "Job Category: Clinical". Also "Employment Type: Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)". Also "Job Summary" paragraph. We need to format using

for section headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We should only include those with real content. We have content for About the role (Job Summary). Responsibilities (Primary Duties...). Requirements (Knowledge And Skills, Education And Experience). Possibly Skills separate? But we can combine Knowledge And Skills as Skills section. Requirements could be Education And Experience. Or we could have Requirements (Education And Experience) and Skills (Knowledge And Skills). We'll decide. Pay: Onsite Rate: $60/hr. Schedule: Total Hours/week: 40.00, 1st Shift, Duration: 12 Months. We also need to include location etc maybe in a short

before sections. We must not repeat job title as heading. So no heading for Senior Clinical Lab Research Specialist. We must not include duplicated lines. We need to preserve all substantive info; do not invent or summarize away detail. So we need to keep specifics like "Calibration of equipment , generate date , read data , Analysis." Might be weird phrasing but we keep. We need to keep "Phelbotmy experience is a plus, follow protocal,sample handling add instrument experience see list below Hepatitis Vaccine required". Keep as is. We need to keep "BS ASCP MT/MLT CLS Certification check if active". Keep. We need to keep "5 years’ experience". Keep. We need to keep "Phlebotomy is a plus". Keep. We need to keep "Experience with human blood specimen collection products". Keep. We need to keep "Product Trouble shooting as it relates to clinical results". Keep. We need to keep "Strong computer skills". Keep. We need to keep "Strong project planning and budget management skills". Keep. We need to keep "Develop/implement new testing methodologies in collaboration with R&D". Keep. We need to keep "Proven understanding of clinical laboratory testing, blood collection, Urinalysis, POC and LIS/LIMS systems and an ability to apply knowledge to innovative concepts/projects beyond the core clinical laboratory." Keep. We need to keep "Education And Experience BS/BA/MA in Clinical Laboratory Science or Medical Technology, Biology Life Sciences or health related field required. MT/MLT CLS (ASCP) or equivalent experience in a Research environment 5 years+ experience in the Clinical Laboratory environment." Keep. We need to keep "Job Summary This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices, as well as provide innovative ideas cross functionally with other business units. Possess a technical competence and works with human blood in clinical laboratory disciplines such as phlebotomy, chemistry, hematology, coagulation, urinalysis, point of care and capable operation of numerous instrument platforms. Responsible for managing clinical laboratory studies and complaint testing through a variety of clinical testing methods. Knowledge and expertise demonstrating safety and efficacy of new or modified in-vitro diagnostic devices, as well provide innovative ideas outside of the core business. Develop/implement new testing methodologies in collaboration with R&D. Responsible for understanding product design, function and able to apply quality and regulatory standards. Utilizes technical/scientific judgment to resolve technical issues. Works with many different disciplines (manufacturing, marketing, quality, regulatory, etc.), materials, products and processes in the development of core clinical laboratory and outside the core clinical laboratory products and services. Possesses a strong commitment to quality and continuous improvement." Keep. We need to keep "Primary Duties, Responsibilities & Authorities Provides input to and conducts scientific investigations in areas of considerable scope and complexity. Explores, identifies and recommends solution, concepts and principles. Adapts methodologies as needed for areas related to the core clinical laboratory. Conducts clinical testing, maintains laboratory instrumentation/reagent test systems and inventory to strategically align with the priorities within the lab and business objectives. Implements and documents Quality Assurance and Quality Control procedures as they pertain to instrumentation and methodology. Conducts instrument verification per CLSI guidelines, assists with updates and preparation of procedures and instrument performance documentation in compliance with GLP and GCP. Keeps current in the field of Clinical Laboratory Science through review of technical literature, participation in continuing education via webinars/symposia and or customer visits. Senses and monitors trends in laboratory practices and utilizes this information to recommend new projects and influence ongoing projects. Participates in development of the clinical strategy for all BD IDS- Specimen Management products and is responsible for generation of scientific and clinical information to support product conceptualization, feasibility and development. Responsible for scientific integrity and clinical accuracy of all claims and communications made concerning specific PAS products globally. Responsible for management of individual focused projects to complex projects involving multiple internal clinical studies/evaluations. This position provides support from a base of clinical experience and knowledge to resolve customer complaints through clinical investigations. This position will also provide support to guide and implement innovation, product development, clinical testing, manufacturing, and post market surveillance via interfacing with R&D and GCD to insure successful and timely completion of projects." Keep. We need to keep "Knowledge And Skills Strong working knowledge of clinical laboratory science Excellent verbal and written communications skills Awareness/basic knowledge of GCP/GLP and ISO regulations Phlebotomy is a plus Experience with human blood specimen collection products Product Trouble shooting as it relates to clinical results Strong computer skills Strong project planning and budget management skills Develop/implement new testing methodologies in collaboration with R&D Proven understanding of clinical laboratory testing, blood collection, Urinalysis, POC and LIS/LIMS systems and an ability to apply knowledge to innovative concepts/projects beyond the core clinical laboratory." Keep. We need to keep "Education And Experience BS/BA/MA in Clinical Laboratory Science or Medical Technology, Biology Life Sciences or health related field required. MT/MLT CLS (ASCP) or equivalent experience in a Research environment 5 years+ experience in the Clinical Laboratory environment." Keep. We need to include Pay: Onsite Rate: $60/hr. Schedule: Total Hours/week: 40.00, 1st Shift, Duration: 12 Months. Location etc: we can put in a paragraph: "

Location: Franklin Lakes, NJ | Duration: 12 Months | Hours/week: 40.00 (1st Shift) | Client: Medical Devices Company | Job Category: Clinical | Employment Type: Contract on W2 (US Citizens/GC Holders/GC EAD/OPT/EAD/CPT)

" We also need to mention panel drug test required. Could be included in that paragraph or separate note. We'll add: "Panel drug test required." We also need to mention Hepatitis Vaccine required. Could be in responsibilities or a note. We'll add a short paragraph after responsibilities maybe. We must not create sections with filler. We'll include About the role (Job Summary), Responsibilities (Primary Duties...), Requirements (Education And Experience), Skills (Knowledge And Skills), Pay, Schedule. We need to use

• for any list of duties/requirements/benefits. The responsibilities and knowledge/skills are prose paragraphs, not lists. However we could convert them to lists? The rule says use
  • for any list of duties/requirements/benefits. If we keep as prose, we should use

    . That's fine. Only if there is a list we need to use

    • . There's no explicit list in the posting; it's all sentences. So we will use

      . We need to output only HTML fragment, no /, no markdown fences. Let's craft. Structure:

      Location: Franklin Lakes, NJ | Duration: 12 Months | Hours/week: 40.00 (1st Shift) | Client: Medical Devices Company | Job Category: Clinical | Employment Type: Contract on W2 (US Citizens/GC Holders/GC EAD/OPT/EAD/CPT) | Panel drug test required.

      About the role

      [Job Summary text]

      Responsibilities

      [Primary Duties text]

      Requirements

      [Education And Experience text]

      Skills

      [Knowledge And Skills text]

      Pay

      Onsite Rate: $60/hr

      Schedule

      Total Hours/week: 40.00, 1st Shift, Duration: 12 Months

      We might also need to mention Hepatitis Vaccine required. Could add a short paragraph after Responsibilities or in a separate section like "Additional Requirements". But we shouldn't create a section unless real specific content. We could add a note in Responsibilities or Requirements. Perhaps add a sentence: "Hepatitis Vaccine required." We'll incorporate into Responsibilities paragraph after the main text. Similarly "BS ASCP MT/MLT CLS Certification check if active" is a requirement; we can include in Requirements paragraph. We need to preserve all details: include "Calibration of equipment , generate date , read data , Analysis." "Phelbotmy experience is a plus, follow protocal,sample handling add instrument experience see list below Hepatitis Vaccine required". We'll embed that in Responsibilities maybe. Let's extract the exact text from posting for each section. Job Summary text: "This laboratory-based position will provide input to design, evaluation, execution and reporting for safety and efficacy of new or modified in-vitro diagnostic devices, as well as provide innovative ideas cross functionally with other business units. Possess a technical competence and works with human blood in clinical laboratory disciplines such as phlebotomy, chemistry, hematology, coagulation, urinalysis, point of care and capable operation of numerous instrument platforms. Responsible for managing clinical laboratory studies and complaint