Clinical Research Coordinator II - Oncology
or drop it. Address could be minor metadata; we could drop or include in a p. Probably drop. We must not create sections with filler like "commensurate with experience". Not needed. We need to output only HTML fragment, no /. Use
for section headings. Use - for any list of duties/requirements/benefits. Use
for prose.
We need to preserve ALL substantive information; do not invent or summarize away detail.
Let's extract details.
From posting:
Our Promise To You Joining AdventHealth is about being part of something bigger... (mission). Could be considered "About the role"? Might be better to put under a section "About the role" as prose.
Job Description paragraph: "Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation. Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity issues. Detail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties Other duties as assigned. Reviews informed consent documents with study candidates and ensures patient advocacy and informed consent throughout the trial. Coordinates support staff, laboratory technicians, and assistants to ensure efficient and high-quality results. Serves as a liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs. Prepares and reviews documentation for clinical research study start-up, execution, modification, renewal, and termination. Maintains current knowledge of regulatory requirements and implements changes as needed. Collaborates with study sponsors and assists site monitors during visits. Works flexible hours and is available for research project-related questions. Communicates effectively with healthcare team members, patients, investigators, sponsors, and administration. Manages records, study medication, and test articles confidentially and securely."
That's responsibilities.
Knowledge, Skills, And Abilities section: list of abilities.
Education: Bachelor's [Required]
Work Experience: 2+ clinical research. [Required]; Cardiology experience [Preferred]; Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines. [Required]
Additional Information: equivalent combination etc.
Licenses And Certifications: Certified Clinical Research Coordinator (CCRC) [Preferred]; Basic Life Support - CPR Cert (BLS) [Preferred]; Advanced Cardiac Life Support Cert (ACLS) [Preferred]
Physical Requirements: link (maybe drop as boilerplate? It's a link to physical requirements; could be considered minor metadata; we could drop or include as a p. Probably drop as it's just a link.
Pay Range: $56,472.00 - $105,040.00
Benefits: list after "All the benefits and perks you need for you and your family: Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability InsurancePaid Time Off from Day One403-B Retirement Plan4 Weeks 100% Paid Parental LeaveCareer DevelopmentWhole Person Well-being ResourcesMental Health Resources and SupportPet Benefits"
We need to separate items properly. The text seems concatenated; we need to parse: Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance Paid Time Off from Day One 403-B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits
We'll make a list.
Schedule: "Schedule Full time Shift Day (United States of America)". Could be under Schedule section.
Address etc: we can drop.
Now decide sections:
- About the role: maybe include the mission statement? Could be considered "About the role" but it's more about organization. Could also omit if not specific to role. The instruction: include a section ONLY when the posting has real, specific content for it. The mission statement is generic; maybe not specific to role. Better to omit About the role section unless we have role-specific overview. The first paragraph "Our Promise To You..." is not role-specific. So we could skip About the role.
- Responsibilities: we have the job description paragraph; we can turn into
or list? It's prose; we can put in
. Could also break into
- for each duty but it's long. The rule: Use
- for any list of duties/requirements/benefits. The job description is not a list but a paragraph; we can keep as
. However there are many sentences; we could split into list but not required. We'll keep as
.
- Requirements: could include Education, Work Experience, Additional Information (equivalent combination). That's requirements.
- Qualifications: could include Licenses And Certifications.
- Skills: Knowledge, Skills, And Abilities.
- Benefits: list.
- Pay: Pay Range.
- Schedule: schedule line.
We must not repeat job title.
Now produce HTML.
We'll need to ensure we don't include boilerplate like "Physical Requirements: (Please click the link below to view work requirements) Physical Requirements - https://tinyurl.com/msy4mja2". That's a link; could be considered minor metadata; we can drop.
Also "This facility is an equal opportunity employer..." drop.
Now craft.
Section headings:
Responsibilities
, Requirements
, Qualifications
, Skills
, Benefits
, Pay
, Schedule
.
We might also include About the role
if we decide to include mission statement; but I'd skip.
Now content:
Responsibilities: Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation. Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity issues. Detail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure. Simultaneously executes and coordinates multiple clinical trials and functions independently; performs diverse clinical and clerical duties. Other duties as assigned. Reviews informed consent documents with study candidates and ensures patient advocacy and informed consent throughout the trial. Coordinates support staff, laboratory technicians, and assistants to ensure efficient and high-quality results. Serves as a liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs. Prepares and reviews documentation for clinical research study start-up, execution, modification, renewal, and termination. Maintains current knowledge of regulatory requirements and implements changes as needed. Collaborates with study sponsors and assists site monitors during visits. Works flexible hours and is available for research project-related questions. Communicates effectively with healthcare team members, patients, investigators, sponsors, and administration. Manages records, study medication, and test articles confidentially and securely.
Requirements: We need to list Education, Work Experience, Additional Information.
Education: Bachelor's [Required]
Work Experience: 2+ clinical research. [Required]; Cardiology experience [Preferred]; Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines. [Required]
Additional Information: An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement: Bachelors degree and 2+ years of experience OR Associates degree and 4+ years of experience OR Technical/Vocational School and 6+ years of clinical research experience. Other certification as applicable to degree or program (i.e., medical assistant, medical technician, phlebotomy)
We can format as - for each bullet.
But note: The instruction: Use
- for any list of duties/requirements/benefits. So we should list requirements as list.
Thus:
- Education: Bachelor's degree required.
- Work Experience: Minimum 2+ years of clinical research required; cardiology experience preferred.
- Work Experience: Research experience including awareness of FDA/OHRP/ICH/GCP guidelines and relevant state/federal regulatory/statutory guidelines required.
- Alternative qualifications: Equivalent combination of education and experience accepted (Bachelor's + 2 years, Associate's + 4 years, Technical/Vocational + 6 years clinical research). Other relevant certifications (e.g., medical assistant, medical technician, phlebotomy) may be considered.
But we need to preserve all detail; we must not lose any. Let's capture exactly:
- Education Bachelor's [Required]
- Work Experience 2+ clinical research. [Required]
- Cardiology experience [Preferred]
- Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines. [Required]
- Additional Information: An equivalent combination of education ad relevant work experience may be considered in lieu of the stated degree requirement: Bachelors degree and 2+ years of experience ORAssociates degree and 4+ years of experience ORTechnical/Vocational School and 6+ years of clinical research experience.Other certification as applicable to degree or program (i.e., medical assistant, medical technician, phlebotomy)
Note there's a typo "ad" but we keep as is? We should preserve exactly; but we can correct minor typos? The instruction: Preserve ALL substantive information; do NOT invent or summarize away detail. It doesn't forbid fixing typos? Safer to keep as is but maybe we can keep the text as given. However we can rephrase slightly but must keep meaning. Safer to keep the exact phrases.
Thus list items:
- Education: Bachelor's [Required]
- Work Experience: 2+ clinical research. [Required]
- Cardiology experience [Preferred]
- Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines. [Required
for prose. We need to preserve ALL substantive information; do not invent or summarize away detail. Let's extract details. From posting: Our Promise To You Joining AdventHealth is about being part of something bigger... (mission). Could be considered "About the role"? Might be better to put under a section "About the role" as prose. Job Description paragraph: "Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation. Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity issues. Detail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties Other duties as assigned. Reviews informed consent documents with study candidates and ensures patient advocacy and informed consent throughout the trial. Coordinates support staff, laboratory technicians, and assistants to ensure efficient and high-quality results. Serves as a liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs. Prepares and reviews documentation for clinical research study start-up, execution, modification, renewal, and termination. Maintains current knowledge of regulatory requirements and implements changes as needed. Collaborates with study sponsors and assists site monitors during visits. Works flexible hours and is available for research project-related questions. Communicates effectively with healthcare team members, patients, investigators, sponsors, and administration. Manages records, study medication, and test articles confidentially and securely." That's responsibilities. Knowledge, Skills, And Abilities section: list of abilities. Education: Bachelor's [Required] Work Experience: 2+ clinical research. [Required]; Cardiology experience [Preferred]; Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines. [Required] Additional Information: equivalent combination etc. Licenses And Certifications: Certified Clinical Research Coordinator (CCRC) [Preferred]; Basic Life Support - CPR Cert (BLS) [Preferred]; Advanced Cardiac Life Support Cert (ACLS) [Preferred] Physical Requirements: link (maybe drop as boilerplate? It's a link to physical requirements; could be considered minor metadata; we could drop or include as a p. Probably drop as it's just a link. Pay Range: $56,472.00 - $105,040.00 Benefits: list after "All the benefits and perks you need for you and your family: Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability InsurancePaid Time Off from Day One403-B Retirement Plan4 Weeks 100% Paid Parental LeaveCareer DevelopmentWhole Person Well-being ResourcesMental Health Resources and SupportPet Benefits" We need to separate items properly. The text seems concatenated; we need to parse: Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance Paid Time Off from Day One 403-B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits We'll make a list. Schedule: "Schedule Full time Shift Day (United States of America)". Could be under Schedule section. Address etc: we can drop. Now decide sections: - About the role: maybe include the mission statement? Could be considered "About the role" but it's more about organization. Could also omit if not specific to role. The instruction: include a section ONLY when the posting has real, specific content for it. The mission statement is generic; maybe not specific to role. Better to omit About the role section unless we have role-specific overview. The first paragraph "Our Promise To You..." is not role-specific. So we could skip About the role. - Responsibilities: we have the job description paragraph; we can turn into
or list? It's prose; we can put in
. Could also break into
- for each duty but it's long. The rule: Use
- for any list of duties/requirements/benefits. The job description is not a list but a paragraph; we can keep as
. However there are many sentences; we could split into list but not required. We'll keep as
. - Requirements: could include Education, Work Experience, Additional Information (equivalent combination). That's requirements. - Qualifications: could include Licenses And Certifications. - Skills: Knowledge, Skills, And Abilities. - Benefits: list. - Pay: Pay Range. - Schedule: schedule line. We must not repeat job title. Now produce HTML. We'll need to ensure we don't include boilerplate like "Physical Requirements: (Please click the link below to view work requirements) Physical Requirements - https://tinyurl.com/msy4mja2". That's a link; could be considered minor metadata; we can drop. Also "This facility is an equal opportunity employer..." drop. Now craft. Section headings:
Responsibilities
,Requirements
,Qualifications
,Skills
,Benefits
,Pay
,Schedule
. We might also includeAbout the role
if we decide to include mission statement; but I'd skip. Now content: Responsibilities:Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation. Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity issues. Detail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure. Simultaneously executes and coordinates multiple clinical trials and functions independently; performs diverse clinical and clerical duties. Other duties as assigned. Reviews informed consent documents with study candidates and ensures patient advocacy and informed consent throughout the trial. Coordinates support staff, laboratory technicians, and assistants to ensure efficient and high-quality results. Serves as a liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs. Prepares and reviews documentation for clinical research study start-up, execution, modification, renewal, and termination. Maintains current knowledge of regulatory requirements and implements changes as needed. Collaborates with study sponsors and assists site monitors during visits. Works flexible hours and is available for research project-related questions. Communicates effectively with healthcare team members, patients, investigators, sponsors, and administration. Manages records, study medication, and test articles confidentially and securely.
Requirements: We need to list Education, Work Experience, Additional Information. Education: Bachelor's [Required] Work Experience: 2+ clinical research. [Required]; Cardiology experience [Preferred]; Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines. [Required] Additional Information: An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement: Bachelors degree and 2+ years of experience OR Associates degree and 4+ years of experience OR Technical/Vocational School and 6+ years of clinical research experience. Other certification as applicable to degree or program (i.e., medical assistant, medical technician, phlebotomy) We can format as- for each bullet.
But note: The instruction: Use
- for any list of duties/requirements/benefits. So we should list requirements as list.
Thus:
- Education: Bachelor's degree required.
- Work Experience: Minimum 2+ years of clinical research required; cardiology experience preferred.
- Work Experience: Research experience including awareness of FDA/OHRP/ICH/GCP guidelines and relevant state/federal regulatory/statutory guidelines required.
- Alternative qualifications: Equivalent combination of education and experience accepted (Bachelor's + 2 years, Associate's + 4 years, Technical/Vocational + 6 years clinical research). Other relevant certifications (e.g., medical assistant, medical technician, phlebotomy) may be considered.
- for any list of duties/requirements/benefits. So we should list requirements as list.
Thus:
- for each bullet.
But note: The instruction: Use
- for any list of duties/requirements/benefits. The job description is not a list but a paragraph; we can keep as