Clinical Project Associate
Sarah Cannon Research Institute · Tennessee, United States · 1 mo ago
RemoteRemoteAnalystFull-time
We need to output HTML fragment with sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. Must not repeat job title. No Job ID. Remove boilerplate, navigation, legal, EEO, scam warning, application instructions. Must preserve all substantive info.
Let's parse the posting.
Content:
Intro: "It’s More Than a Career, It’s a Mission..." etc. That's about the role? Could be "About the role". We'll include that as prose.
Then: "As the Clinical Project Associate, you are responsible for ensuring the Trial Master File (TMF) is set-up and maintained in “audit ready” condition; and conduct critical documentation collection and review throughout the lifecycle of the study, in accordance with Good Clinical Practices, ICH Guidelines, Federal Regulations and Development Innovations SOPs. You will maintain clinical trial management systems and tracking tools, actively participating in cross-functional teams to ensure delivery of project deliverables. This position is remote based in the US; relocation assistance and visa sponsorship are not available."
That's responsibilities.
Then bullet list of duties: "Duties include and are not limited to: You will set-up, document collection/upload of files to the TMF/eTMF You will perform initial quality review of documents prior to upload/filing in the TMF/eTMF You will partner with document specialist to maintain the Trial Master File (TMF) in “audit ready” condition from study start to completion You will assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial You perform critical document distribution to and collection from the investigative sites throughout the lifecycle of the clinical trial. Proactively liaise with Clinical Research Associate and investigative site to resolve outstanding regulatory issues You review study documents to ensure they are current, complete and accurate Other duties as assigned"
We need to format as
- each duty.
Then "Qualifications needed: Minimum High School Diploma or GED At least 1 year of clinical research experience required; at least 3 years of clinical research experience preferred. Oncology clinical research experience preferred"
That's qualifications.
Then "About Sarah Cannon Research Institute (SCRI) ..." That's about the company, maybe "About the role"? Actually we already have about the role earlier. Could have "About the company" but not in allowed headings. Allowed headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. So we can put company description under "About the role" maybe combine with intro. Or we could put under "About the role" as description of the organization. That's fine.
Then "We care about the well-being..." that's benefits. So we need Benefits section.
Then "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."
That's Pay section.
Then scam warning etc is boilerplate to remove.
EEO statement also boilerplate to remove.
Thus we have sections: About the role (intro + company description), Responsibilities (including the paragraph and bullet list), Qualifications (education + experience), Benefits, Pay.
We might also include Requirements? The qualifications needed could be considered Requirements. But we have Qualifications heading. The allowed headings include Requirements and Qualifications both. We need to decide which to use. The posting has "Qualifications needed:" which is qualifications. Could also treat "Minimum High School Diploma or GED..." as Requirements. But we have both headings; we should not duplicate content. Choose one. Since they explicitly say "Qualifications needed:", we can use Qualifications heading. Requirements could be omitted if no separate content.
Skills: Not explicitly listed; maybe we could infer but we should not invent. So omit Skills.
Schedule: Not mentioned; remote based in US but no schedule details. So omit.
Thus output HTML with sections: About the role, Responsibilities, Qualifications, Benefits, Pay.
Make sure each section heading is
. Then content:
for prose,
- for lists.
We need to preserve all substantive information. Let's extract exact sentences.
About the role: combine intro paragraphs and company description.
Intro: "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."
Then company description: "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." The "Please click here..." is a link; we should keep the sentence but maybe it's a navigation? It's a call to action but it's substantive? It's a link to learn more; could be considered boilerplate? It's not navigation but it's a reference. Probably we can keep it as prose.
We also have "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." That's benefits; we will put in Benefits section.
Thus About the role section should include the mission/intro and company description but not the benefits part (that goes to Benefits). Also not the compensation part (goes to Pay). Also not the scam warning etc.
Now Responsibilities: include the paragraph about ensuring TMF etc and the bullet list.
Paragraph: "As the Clinical Project Associate, you are responsible for ensuring the Trial Master File (TMF) is set-up and maintained in “audit ready” condition; and conduct critical documentation collection and review throughout the lifecycle of the study, in accordance with Good Clinical Practices, ICH Guidelines, Federal Regulations and Development Innovations SOPs. You will maintain clinical trial management systems and tracking tools, actively participating in cross-functional teams to ensure delivery of project deliverables. This position is remote based in the US; relocation assistance and visa sponsorship are not available."
Then bullet list items: need to split each duty.
List items as given:
- You will set-up, document collection/upload of files to the TMF/eTMF
- You will perform initial quality review of documents prior to upload/filing in the TMF/eTMF
- You will partner with document specialist to maintain the Trial Master File (TMF) in “audit ready” condition from study start to completion
- You will assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial
- You perform critical document distribution to and collection from the investigative sites throughout the lifecycle of the clinical trial.
- Proactively liaise with Clinical Research Associate and investigative site to resolve outstanding regulatory issues
- You review study documents to ensure they are current, complete and accurate
- Other duties as assigned
Note some sentences missing "You will". We'll keep as is.
Now Qualifications: "Minimum High School Diploma or GED At least 1 year of clinical research experience required; at least 3 years of clinical research experience preferred. Oncology clinical research experience preferred"
We can format as
- each? Could be prose. We'll use
- for list.
Now Benefits: "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."
We keep that.
Now Pay: "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 ensure we removed boilerplate: EEO, scam warning, application instructions (like "Please click here to learn more about our research offerings." that's okay? It's a link but it's not application instruction. It's about research offerings; we kept it in About the role. The "Please click here to learn more about our research offerings." is a link; we keep as prose. Similarly "For more information regarding benefits through our parent company, McKesson, please click here." we kept in Benefits. That's okay.
Now output HTML fragment.
Structure:
About the role
... (combined intro and company description)
Responsibilities
... paragraph
- ... ...
Qualifications
- Minimum High School Diploma or GED
- At least 1 year of clinical research experience required; at least 3 years of clinical research experience preferred.
- Oncology clinical research experience preferred
Benefits
... benefits paragraph
Pay
... pay paragraph
Make sure no extra whitespace? It's fine. Now craft the About the role paragraph: combine the mission intro and company description. Let's write: "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. 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
- for list.
Now Benefits: "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."
We keep that.
Now Pay: "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 ensure we removed boilerplate: EEO, scam warning, application instructions (like "Please click here to learn more about our research offerings." that's okay? It's a link but it's not application instruction. It's about research offerings; we kept it in About the role. The "Please click here to learn more about our research offerings." is a link; we keep as prose. Similarly "For more information regarding benefits through our parent company, McKesson, please click here." we kept in Benefits. That's okay.
Now output HTML fragment.
Structure:
- each? Could be prose. We'll use
- for lists.
We need to preserve all substantive information. Let's extract exact sentences.
About the role: combine intro paragraphs and company description.
Intro: "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."
Then company description: "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." The "Please click here..." is a link; we should keep the sentence but maybe it's a navigation? It's a call to action but it's substantive? It's a link to learn more; could be considered boilerplate? It's not navigation but it's a reference. Probably we can keep it as prose.
We also have "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." That's benefits; we will put in Benefits section.
Thus About the role section should include the mission/intro and company description but not the benefits part (that goes to Benefits). Also not the compensation part (goes to Pay). Also not the scam warning etc.
Now Responsibilities: include the paragraph about ensuring TMF etc and the bullet list.
Paragraph: "As the Clinical Project Associate, you are responsible for ensuring the Trial Master File (TMF) is set-up and maintained in “audit ready” condition; and conduct critical documentation collection and review throughout the lifecycle of the study, in accordance with Good Clinical Practices, ICH Guidelines, Federal Regulations and Development Innovations SOPs. You will maintain clinical trial management systems and tracking tools, actively participating in cross-functional teams to ensure delivery of project deliverables. This position is remote based in the US; relocation assistance and visa sponsorship are not available."
Then bullet list items: need to split each duty.
List items as given:
- You will set-up, document collection/upload of files to the TMF/eTMF
- You will perform initial quality review of documents prior to upload/filing in the TMF/eTMF
- You will partner with document specialist to maintain the Trial Master File (TMF) in “audit ready” condition from study start to completion
- You will assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial
- You perform critical document distribution to and collection from the investigative sites throughout the lifecycle of the clinical trial.
- Proactively liaise with Clinical Research Associate and investigative site to resolve outstanding regulatory issues
- You review study documents to ensure they are current, complete and accurate
- Other duties as assigned
Note some sentences missing "You will". We'll keep as is.
Now Qualifications: "Minimum High School Diploma or GED At least 1 year of clinical research experience required; at least 3 years of clinical research experience preferred. Oncology clinical research experience preferred"
We can format as