Clinical Trials Screening Coordinator I - GI

We need to output HTML fragment with sections: headings

for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. Remove boilerplate like EEO, accommodation, etc. Also remove application instructions, navigation, cookie, legal, duplicated lines. We need to parse the posting. Key content: - Intro: Working at Moffitt is both a career and a mission... (summary). Could be "About the role" or maybe "About Moffitt". The instruction: use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we can create sections: About the role (or About Moffitt), Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to preserve all substantive info. Let's extract: About the role / Moffitt: "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." Also 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 Trials Screening 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 Trials Screening 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 Trials Screening 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." That could be part of About the role. Responsibilities: The posting includes details: "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." Also: "Clinical Trials 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." Also: "The Clinical Trials Screening Coordinator I reports to the Clinical Trials Office but will directly support a specific Disease Site Program. This position is embedded in the clinic to serve as a single point of contact to aid physicians, clinical team - members and research personnel with timely identification of patients for consideration for clinical trial enrollment. The role performs an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program. The role has the primary responsibility for referring physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials. This is role is within the clinical trials career path supporting the PI in clinical trials." Also: "Successful Candidates Will Possess Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences Prior experience in clinical trials is preferred Familiarity with regulatory requirements in clinical research or ability to successfully learn this Experience interacting with patients and coordinating care with medical staff Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol" That's more like Requirements/Skills. Minimum Requirements: "Bachelor's degree in science, health-related field or related project management. 2 years' experience in clinical trials (patient-facing coordination, data management, regulatory or other research coordination)." Salary Range: "$29.05 - $44.28" with note. Schedule: "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 need to avoid filler like "commensurate with experience". Not present. We need to output only HTML fragment, no markdown fences. We'll create sections:

About the role

with paragraphs summarizing Moffitt and role.

Responsibilities

with ul li for responsibilities.

Minimum Requirements

maybe as Requirements.

Preferred Qualifications

maybe as Qualifications (but we have "Successful Candidates Will Possess" list). Could be Skills. We need to decide mapping. We have: - About the role: intro + summary. - Responsibilities: list of duties: work closely with patients, families, sponsors, trial team; report to Clinical Trials Office, support Disease Site Program; embedded in clinic as single point of contact; aid physicians, team, research personnel with timely identification of patients for trial enrollment; integrated approach to ensure effectiveness/efficiencies for directing potential patients to trial program; primary responsibility for referring physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials; within clinical trials career path supporting PI. - Requirements: Bachelor's degree in science, health-related field or related project management; 2 years' experience in clinical trials (patient-facing coordination, data management, regulatory or other research coordination). - Qualifications/Skills: Effective communication, good decision-making, eagerness to embrace challenges with sense of urgency and enthusiasm, time management skills; excellent teamwork skills and ability to collaborate with diverse backgrounds; prior experience in clinical trials preferred; familiarity with regulatory requirements in clinical research or ability to learn; experience interacting with patients and coordinating care with medical staff; gain solid learning and understanding of regulatory guidelines and following a clinical trial protocol. - Benefits: Paid training and orientation through CTO Academy; position tiers may vary according to experience; relocation assistance may be provided. - Pay: Salary Range $29.05 - $44.28 (with note about actual compensation may vary based on location etc.) - Schedule: Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. We should not include filler like "Position tiers may vary according to experience." That's substantive enough for Benefits? It's more about role classification. Could be under Benefits or maybe under About the role. But we can include in Benefits as "Position tiers may vary according to experience." It's not a benefit per se but it's info. However we need to only include sections when posting has real specific content. It does have that sentence. Could be placed under Benefits or maybe under About the role. I'd put under Benefits as it's a detail about the role. But we also have "Relocation assistance may be provided." That's a benefit. Thus Benefits section: Paid training and orientation through CTO Academy; Position tiers may vary according to experience; Relocation assistance may be provided. Now we need to avoid duplication: The sentence about hybrid work appears also in Schedule. We'll put that in Schedule. Now we need to ensure we don't include boilerplate: EEO, accommodation, etc. Remove. Now produce HTML:

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 Trials Screening 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 Trials Screening 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 Trials Screening 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.

Responsibilities

• 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.
• Report to the Clinical Trials Office and directly support a specific Disease Site Program.
• Serve as an embedded single point of contact in the clinic to aid physicians, clinical team members, and research personnel with timely identification of patients for consideration for clinical trial enrollment.
• Perform an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program.
• Have primary responsibility for referring physicians, patients, and caregivers to guide, review eligibility, and provide access to available clinical trials.
• Support the principal investigator within the clinical trials career path.

Requirements

• Bachelor's degree in science, health‑related field or related project management.
• 2 years' experience in clinical trials (patient‑facing coordination, data management, regulatory or other research coordination).

Skills

• Effective communication, good decision‑making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills.
• Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences.
• Prior experience in clinical trials is preferred.
• Familiarity with regulatory requirements in clinical research or ability to successfully learn this.
• Experience interacting with patients and coordinating care with medical staff.
• Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol.

Benefits

• Paid training and orientation through the CTO (Clinical Trials Office) Academy.
• Position tiers may vary according to experience.
• Relocation assistance may be provided.

Pay

Salary Range $29.05 – $44.28 (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).

Schedule

Monday through Friday schedule with hybrid work (mix of remote and on‑site) after passing a 90‑day introductory and training period.

Check for any leftover boilerplate: We removed EEO, accommodation, etc. Also removed the link and "Clinical Trials These positions work closely..." we incorporated into responsibilities. Also removed "Moffitt Career Site" etc. We kept all substantive info