Manager of Clinical Research Support
for each heading. Use - for any list of duties/requirements/benefits. Use
for prose. Do NOT repeat job title as heading. Do NOT put Job ID/requisition numbers as headings. Remove boilerplate, navigation, legal, EEO, scam warning, duplicated lines, application instructions. Preserve all substantive info. Include a section only when posting has real, specific content. Avoid filler like "commensurate with experience". No Pay/Schedule/Benefits unless posting actually states them.
Let's extract content.
Job description: "Our Manager Clinical Research Support will oversee and manage the clinical support operations ensuring regulatory compliance, operational excellence, and exceptional patient experience. Additionally, this position is responsible for managing and developing a multidisciplinary team of Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, Program Managers, Executive Support, Medical Assistants, and Front Desk Coordinators and for optimizing workflows. This position is onsite at our Dallas, TX clinic. Relocation assistance is not available."
Then duties list: "Provide direct supervision, mentorship, and performance management for Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, and Program Manager, Executive Support staff, Medical Assistants, and Front Desk Coordinators. Oversee and optimize all aspects of clinical support including biospecimen collection, processing, shipping, and documentation in accordance with protocol and regulatory requirements Coordinate and oversee the collection of vital signs, ECGs, and laboratory specimens, ensuring protocol adherence and data integrity. Ensure the highest standards of patient safety and confidentiality throughout all clinic and research activities. Develop, implement, and monitor departmental SOPs, work instructions, and ensure alignment with corporate and regulatory guidelines"
Minimum qualifications: "Associate's degree in clinical research, healthcare, or related field obtained, Bachelor's Degree preferred 1+ years' work experience in clinical trial operations, including regulatory, safety, and biospecimen management requirements Expertise focused in GCP, GLP, HIPAA, OSHA, and IATA regulations Experience in research protocol interpretation and clinical trial management systems Advanced experience in all Microsoft Office products including Excel, Word, SharePoint, PowerPoint as well as EMR experience Strong proficiency in clinical trial databases, electronic data capture needed Experience adapting to a rapidly changing clinical and research environment as well as prioritizing multiple tasks simultaneously."
About SCRI: paragraph about SCRI.
Total Rewards: "We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here."
Compensation: "As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered."
Scam warning and EEO etc should be removed.
We need sections: About the role (maybe a summary), Responsibilities (duties), Requirements (minimum qualifications), Qualifications (maybe preferred?), Skills (maybe expertise?), Benefits (Total Rewards), Pay (compensation), Schedule (maybe not given). There's no explicit schedule info. So we should not create Schedule section.
We need to decide which sections to include based on content.
- About the role: Could be the introductory paragraph about the role (mission, overview). We have "Our Manager Clinical Research Support will oversee and manage..." That's role description. Also mission statement earlier. Could combine.
- Responsibilities: Duties list.
- Requirements: Minimum qualifications.
- Qualifications: Maybe preferred qualifications (Bachelor's preferred). Could be separate.
- Skills: Expertise in regulations, Microsoft Office, EMR, clinical trial databases, etc.
- Benefits: Total Rewards paragraph.
- Pay: Compensation paragraph.
We must not create sections with filler. Ensure each heading has substantive content.
We must not repeat job title as heading. So no heading "Manager Clinical Research Support". Use generic headings.
We must not include Job ID etc.
We must not include boilerplate like EEO, scam warning, application instructions, navigation.
We must preserve all substantive info; do not invent or summarize away detail. So we need to keep details like "onsite at our Dallas, TX clinic. Relocation assistance is not available." Should be included somewhere, maybe in About the role or Responsibilities.
We need to format lists with
- . For duties, we have multiple sentences; we can split into list items.
Similarly for qualifications, we can list each bullet.
We need to ensure we don't lose any detail.
Let's extract details precisely.
Intro paragraph: "It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world."
That's a lot of fluff but it's substantive? It's about mission. Could be part of About the role.
Then role description: "Our Manager Clinical Research Support will oversee and manage the clinical support operations ensuring regulatory compliance, operational excellence, and exceptional patient experience. Additionally, this position is responsible for managing and developing a multidisciplinary team of Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, Program Managers, Executive Support, Medical Assistants, and Front Desk Coordinators and for optimizing workflows. This position is onsite at our Dallas, TX clinic. Relocation assistance is not available."
Duties list: after "Duties include and are not limited to:" then list.
Let's capture each duty as separate bullet:
- Provide direct supervision, mentorship, and performance management for Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, and Program Manager, Executive Support staff, Medical Assistants, and Front Desk Coordinators.
- Oversee and optimize all aspects of clinical support including biospecimen collection, processing, shipping, and documentation in accordance with protocol and regulatory requirements
- Coordinate and oversee the collection of vital signs, ECGs, and laboratory specimens, ensuring protocol adherence and data integrity.
- Ensure the highest standards of patient safety and confidentiality throughout all clinic and research activities.
- Develop, implement, and monitor departmental SOPs, work instructions, and ensure alignment with corporate and regulatory guidelines
Minimum qualifications: after "Minimum qualifications needed include:" then list.
Let's capture each:
- Associate's degree in clinical research, healthcare, or related field obtained
- Bachelor's Degree preferred
- 1+ years' work experience in clinical trial operations, including regulatory, safety, and biospecimen management requirements
- Expertise focused in GCP, GLP, HIPAA, OSHA, and IATA regulations
- Experience in research protocol interpretation and clinical trial management systems
- Advanced experience in all Microsoft Office products including Excel, Word, SharePoint, PowerPoint as well as EMR experience
- Strong proficiency in clinical trial databases, electronic data capture needed
- Experience adapting to a rapidly changing clinical and research environment as well as prioritizing multiple tasks simultaneously.
About SCRI paragraph: "Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings."
We should keep that but remove the "Please click here" maybe it's a link; but it's still substantive? It's a reference; we can keep as text but maybe it's considered navigation? It's a link to learn more; but it's not boilerplate; it's part of description. We'll keep as sentence but maybe we can drop the "Please click here" as it's just a call to action; but it's not essential. However we must preserve ALL substantive information; the link is not substantive info; it's a reference. Could drop. Safer to keep the sentence without the link? The instruction: "Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions." The "Please click here to learn more about our research offerings." is like a navigation instruction; could be considered navigation. Safer to remove that sentence.
Total Rewards: "We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here."
Again the "please click here" maybe navigation; we can drop that sentence.
Compensation: "As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered."
We keep that.
Now we need to decide sections.
Potential sections:
- About the role (intro + mission + role description)
- Responsibilities (duties)
- Requirements (minimum qualifications)
- Qualifications (preferred: Bachelor's degree)
- Skills (expertise in regulations, Microsoft Office, EMR, clinical trial databases, adaptability)
- Benefits (Total Rewards)
- Pay (compensation)
We should not create Schedule.
Now ensure we don't repeat content across sections unnecessarily but we must preserve all info. Some info may appear in multiple sections; we need to ensure we don't lose any.
Let's craft.
About the role: combine introductory mission paragraphs and role description.
We'll include:
It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
Our Manager Clinical Research Support will oversee and
for prose. Do NOT repeat job title as heading. Do NOT put Job ID/requisition numbers as headings. Remove boilerplate, navigation, legal, EEO, scam warning, duplicated lines, application instructions. Preserve all substantive info. Include a section only when posting has real, specific content. Avoid filler like "commensurate with experience". No Pay/Schedule/Benefits unless posting actually states them. Let's extract content. Job description: "Our Manager Clinical Research Support will oversee and manage the clinical support operations ensuring regulatory compliance, operational excellence, and exceptional patient experience. Additionally, this position is responsible for managing and developing a multidisciplinary team of Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, Program Managers, Executive Support, Medical Assistants, and Front Desk Coordinators and for optimizing workflows. This position is onsite at our Dallas, TX clinic. Relocation assistance is not available." Then duties list: "Provide direct supervision, mentorship, and performance management for Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, and Program Manager, Executive Support staff, Medical Assistants, and Front Desk Coordinators. Oversee and optimize all aspects of clinical support including biospecimen collection, processing, shipping, and documentation in accordance with protocol and regulatory requirements Coordinate and oversee the collection of vital signs, ECGs, and laboratory specimens, ensuring protocol adherence and data integrity. Ensure the highest standards of patient safety and confidentiality throughout all clinic and research activities. Develop, implement, and monitor departmental SOPs, work instructions, and ensure alignment with corporate and regulatory guidelines" Minimum qualifications: "Associate's degree in clinical research, healthcare, or related field obtained, Bachelor's Degree preferred 1+ years' work experience in clinical trial operations, including regulatory, safety, and biospecimen management requirements Expertise focused in GCP, GLP, HIPAA, OSHA, and IATA regulations Experience in research protocol interpretation and clinical trial management systems Advanced experience in all Microsoft Office products including Excel, Word, SharePoint, PowerPoint as well as EMR experience Strong proficiency in clinical trial databases, electronic data capture needed Experience adapting to a rapidly changing clinical and research environment as well as prioritizing multiple tasks simultaneously." About SCRI: paragraph about SCRI. Total Rewards: "We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here." Compensation: "As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered." Scam warning and EEO etc should be removed. We need sections: About the role (maybe a summary), Responsibilities (duties), Requirements (minimum qualifications), Qualifications (maybe preferred?), Skills (maybe expertise?), Benefits (Total Rewards), Pay (compensation), Schedule (maybe not given). There's no explicit schedule info. So we should not create Schedule section. We need to decide which sections to include based on content. - About the role: Could be the introductory paragraph about the role (mission, overview). We have "Our Manager Clinical Research Support will oversee and manage..." That's role description. Also mission statement earlier. Could combine. - Responsibilities: Duties list. - Requirements: Minimum qualifications. - Qualifications: Maybe preferred qualifications (Bachelor's preferred). Could be separate. - Skills: Expertise in regulations, Microsoft Office, EMR, clinical trial databases, etc. - Benefits: Total Rewards paragraph. - Pay: Compensation paragraph. We must not create sections with filler. Ensure each heading has substantive content. We must not repeat job title as heading. So no heading "Manager Clinical Research Support". Use generic headings. We must not include Job ID etc. We must not include boilerplate like EEO, scam warning, application instructions, navigation. We must preserve all substantive info; do not invent or summarize away detail. So we need to keep details like "onsite at our Dallas, TX clinic. Relocation assistance is not available." Should be included somewhere, maybe in About the role or Responsibilities. We need to format lists with
- . For duties, we have multiple sentences; we can split into list items.
Similarly for qualifications, we can list each bullet.
We need to ensure we don't lose any detail.
Let's extract details precisely.
Intro paragraph: "It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world."
That's a lot of fluff but it's substantive? It's about mission. Could be part of About the role.
Then role description: "Our Manager Clinical Research Support will oversee and manage the clinical support operations ensuring regulatory compliance, operational excellence, and exceptional patient experience. Additionally, this position is responsible for managing and developing a multidisciplinary team of Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, Program Managers, Executive Support, Medical Assistants, and Front Desk Coordinators and for optimizing workflows. This position is onsite at our Dallas, TX clinic. Relocation assistance is not available."
Duties list: after "Duties include and are not limited to:" then list.
Let's capture each duty as separate bullet:
- Provide direct supervision, mentorship, and performance management for Lab Research Assistants, Clinical Research Assistants, Tissue Coordinators, and Program Manager, Executive Support staff, Medical Assistants, and Front Desk Coordinators.
- Oversee and optimize all aspects of clinical support including biospecimen collection, processing, shipping, and documentation in accordance with protocol and regulatory requirements
- Coordinate and oversee the collection of vital signs, ECGs, and laboratory specimens, ensuring protocol adherence and data integrity.
- Ensure the highest standards of patient safety and confidentiality throughout all clinic and research activities.
- Develop, implement, and monitor departmental SOPs, work instructions, and ensure alignment with corporate and regulatory guidelines
Minimum qualifications: after "Minimum qualifications needed include:" then list.
Let's capture each:
- Associate's degree in clinical research, healthcare, or related field obtained
- Bachelor's Degree preferred
- 1+ years' work experience in clinical trial operations, including regulatory, safety, and biospecimen management requirements
- Expertise focused in GCP, GLP, HIPAA, OSHA, and IATA regulations
- Experience in research protocol interpretation and clinical trial management systems
- Advanced experience in all Microsoft Office products including Excel, Word, SharePoint, PowerPoint as well as EMR experience
- Strong proficiency in clinical trial databases, electronic data capture needed
- Experience adapting to a rapidly changing clinical and research environment as well as prioritizing multiple tasks simultaneously.
About SCRI paragraph: "Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings."
We should keep that but remove the "Please click here" maybe it's a link; but it's still substantive? It's a reference; we can keep as text but maybe it's considered navigation? It's a link to learn more; but it's not boilerplate; it's part of description. We'll keep as sentence but maybe we can drop the "Please click here" as it's just a call to action; but it's not essential. However we must preserve ALL substantive information; the link is not substantive info; it's a reference. Could drop. Safer to keep the sentence without the link? The instruction: "Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions." The "Please click here to learn more about our research offerings." is like a navigation instruction; could be considered navigation. Safer to remove that sentence.
Total Rewards: "We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here."
Again the "please click here" maybe navigation; we can drop that sentence.
Compensation: "As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered."
We keep that.
Now we need to decide sections.
Potential sections:
- About the role (intro + mission + role description)
- Responsibilities (duties)
- Requirements (minimum qualifications)
- Qualifications (preferred: Bachelor's degree)
- Skills (expertise in regulations, Microsoft Office, EMR, clinical trial databases, adaptability)
- Benefits (Total Rewards)
- Pay (compensation)
We should not create Schedule.
Now ensure we don't repeat content across sections unnecessarily but we must preserve all info. Some info may appear in multiple sections; we need to ensure we don't lose any.
Let's craft.
About the role: combine introductory mission paragraphs and role description.
We'll include:
It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
Our Manager Clinical Research Support will oversee and