We need to output HTML fragment with sections: About the role? The posting includes summary paragraphs, responsibilities, requirements, qualifications, skills, benefits, pay, schedule. We need to include sections only if real content.
We must not repeat job title as heading. No Job ID. Remove boilerplate: EEO, accommodation, legal, etc. Also remove navigation, cookie, etc. Also remove application instructions (like link). Also remove duplicated lines.
We need to preserve substantive info.
Let's extract content:
Intro: "Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces."
Then "Summary Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career. This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided."
Then link (should be removed). Then "These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers."
Then "Clinical Research Coordinator II Position Highlights The Clinical Research Coordinator II (CRC II) is a second level in the CRC career path within Clinical Trials. It is a development career position supporting the PI in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center. The CRC II may also support PI sponsored IND or IDE trials. As the primary resource for the protocols, the CRC II will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines. The CRC II will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, the CRC II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. The CRC II will perform all CRC core support and additional responsibilities of more complex studies, with a higher patient volume in comparison to the CRC I. The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies. The supervisor or Principal Investigator will provide more detailed instructions on new complex assignments where there is limited prior depth, or breadth of knowledge or working experience. Moderate supervision provided while developing latitude for independent judgment. Still developing and acquiring higher level knowledge and skills, while working on moderate scope complexity where analysis of situations or data requires a review of a variety of factors. Solves a range of straight forward problems using prescribed guidelines and policies. Limited problem solving while working under defined guidelines. Continues to build productive internal/external working relationships."
Then "Requirements Education and Experience: Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred Two (2) years of clinical trials coordination experience. Associate's degree considered with two (2) additional years of experience. License/Certification CCRP/CCRC or equivalent preferred"
Then "Knowledge And Skills The CRC II is required to have thorough knowledge of word processing (Microsoft Office Suite), data base entry, and thorough knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research. They should be proficient in the use of EMR systems, clinical trial management systems and various other data capture/reporting systems. This person must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals. A proficient understanding of medical terminology required. The CRC II is required to work under minimal supervision to plan, organize, and coordinate multiple work assignments, establish and maintain effective working relationships with others in a team setting and communicate clearly verbally and in writing. The ability to prioritize assignments and pace one’s-self when working under the pressure of deadlines and work volume is required. This person must successfully demonstrate competency by meeting established competency guideline/checklist annually."
Then "Salary Range $29.05 - $44.28 Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions. We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce."
Then "Moffitt Career Site If you have the vision, passion, and dedication to contribute to our mission, then we have a place for you!" This is like a call to action; maybe we can treat as part of About the role? It's not boilerplate; it's a motivational statement. Could be part of About the role or Summary. We'll keep.
Then EEO etc to be removed.
We need sections: About the role (maybe summary), Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule.
We have schedule info: "This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period."
Benefits: "Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided." Also maybe other benefits not listed.
We have Pay: salary range.
We have Requirements: education/experience, license/certification.
We have Knowledge And Skills: that's skills.
We have Responsibilities: the Position Highlights section describes responsibilities.
We have About the role: intro and summary.
We need to avoid duplicate content.
Let's craft sections:
About the role
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces. Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career. These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Moffitt Career Site If you have the vision, passion, and dedication to contribute to our mission, then we have a place for you!
But we might split some into Responsibilities.
Better: About the role: general description of Moffitt and role purpose.
Responsibilities: list duties from Position Highlights.
Let's extract responsibilities bullet points:
- Supporting the PI in clinical trials by implementing and coordinating research including administrative procedures.
- May also support PI sponsored IND or IDE trials.
- As primary resource for protocols, coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines.
- Act as liaison between investigators, care providers, Moffitt regulatory staff and the sponsor.
- Along with investigator, screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while subjects are on study.
- Perform all CRC core support and additional responsibilities of more complex studies, with higher patient volume compared to CRC I.
- Responsible for determining methods and procedures for coordination of newly assigned studies.
- Supervisor or PI provides detailed instructions on new complex assignments where limited prior depth/breadth.
- Moderate supervision while developing latitude for independent judgment.
- Still developing and acquiring higher level knowledge and skills, working on moderate scope complexity where analysis requires review of variety of factors.
- Solves straightforward problems using prescribed guidelines and policies.
- Limited problem solving while working under defined guidelines.
- Continues to build productive internal/external working relationships.
We can put as
- ... etc.
Requirements: Education and Experience, License/Certification.
We can list as
.
Qualifications: maybe same as Requirements? The instruction says use sections for Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We have Requirements (education/experience, license/cert). Qualifications maybe could be same? But we could treat Qualifications as "Preferred qualifications" maybe none separate. Could combine? But we need to only include sections when there is real specific content. We have Requirements content. We might not have separate Qualifications beyond Requirements. Could skip Qualifications.
Skills: Knowledge And Skills section.
Benefits: paid training/orientation, position tiers may vary, relocation assistance may be provided. Also maybe hybrid work after 90-day period? That's schedule though.
Pay: salary range.
Schedule: Monday through Friday, hybrid after 90-day intro.
Let's craft.
We must not include boilerplate like EEO, accommodation, legal, etc.
We must not include duplicated lines.
We must not include the link.
We must not include "Moffitt Career Site" maybe it's okay as part of About the role but it's a call to action; we can keep.
Now produce HTML fragment.
Let's write:
About the role
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces. Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving