Contractor-Clinical Research Coordinator (Rochester, MI)
for section headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We must not repeat job title. We must not include Job ID etc. Remove boilerplate. Keep substantive info.
We need to parse the posting.
Sections present:
- About Profound Research (intro) – could be "About the role"? Actually "About Profound Research" is company description. Could map to "About the role"? But we have a heading "About the role" allowed. The content about company mission etc is relevant. We'll put under About the role
with paragraphs.
- Responsibilities: list of duties.
- Requirements: education/experience etc.
- Qualifications? Might be similar to Requirements; but we have "Requirements" already. Could also have "Qualifications" maybe separate but we should not create empty sections. The posting includes "Requirements" bullet list; also includes "Travel Requirements", "Physical Requirements & Work Environment". Those could be part of Requirements or separate sections like "Travel Requirements" and "Physical Requirements". But allowed headings are limited to the list; we could put travel and physical under Requirements as subpoints? But we must use only allowed headings. We could include a section "Requirements" and within it include subpoints; but we cannot create custom headings like Travel Requirements. So we can incorporate those details into the Requirements section as paragraphs or list items.
- Benefits: there is "Why Join Profound Research?" includes Meaningful Impact, Professional Growth, Leadership & Advancement, Collaborative Culture, Full Benefits Package, Diverse Clinical Exposure. That's benefits. So we can make Benefits
with list.
- Pay: not specified; do not create Pay section.
- Schedule: not specified; do not create Schedule section.
- Skills: maybe we can extract skills from requirements: "Proficient ability to work independently, plan and prioritize with minimal guidance; Excellent attention to detail, organization, and communication with varied stakeholders; Ability to work as a team player with the ability to adapt to changing schedules and assignments". Could be a Skills section. But we need to see if there is explicit skills content. The posting includes those under Requirements. Could create a Skills section with those items. However we must not invent sections without real content. The skills are present; we can put them under Skills heading.
- Qualifications: maybe we can treat Requirements as Qualifications? But we already have Requirements. Could also have Qualifications separate but content may overlap. Safer to have Requirements and Skills sections; maybe also Qualifications if we have distinct content like certifications (GCP, CCRC). Those are qualifications. Could put under Qualifications.
Let's decide sections:
- About the role (company description, mission, vision, values, why role exists)
- Responsibilities
- Qualifications (certifications, experience, education)
- Skills (independent work, attention to detail, teamwork, adaptability)
- Benefits (why join)
We must not include empty headings.
Now we need to preserve all substantive information; not invent or summarize away detail. Must keep details.
We need to format lists with - . For prose use
.
We must not repeat job title.
We must not include boilerplate like cookie/navigation/legal/EEO etc. The posting includes a note about AI tools; that's not boilerplate? It's about hiring process; could be considered substantive? It's about hiring process; maybe we should keep? It's not a standard boilerplate but it's about AI usage. The instruction: Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. The AI note is not exactly those; it's about hiring process. Might be considered part of posting; but it's not about the job itself. Might be considered boilerplate? It's not EEO. It's about AI tools usage in hiring. Could be considered part of the posting but not essential job description. Safer to keep? The instruction says remove boilerplate, duplicated lines, and application instructions. This is not application instructions; it's about AI tools usage. I'd keep it as a paragraph maybe under Benefits or separate? But there is no heading for that. Could add a paragraph after Benefits? But we shouldn't create new heading. Could add a
after Benefits section. That is allowed as part of the HTML fragment (just extra content). However we need to ensure we only output HTML fragment; we can include multiple sections and paragraphs.
Let's extract content.
About Profound Research:
"Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues. Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency. Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards."
Why this Role Exists: "The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values."
We can combine.
Responsibilities list:
- Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
- Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner
- Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills
- Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up
- Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
- Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products
- Other duties as assigned
Requirements:
- Bachelor’s degree and 2 years relevant experience in the life science industry OR
- Associate’s degree with 4 years relevant experience in the life science industry OR
- High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience
- Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Proficient ability to work independently, plan and prioritize with minimal guidance
- Excellent attention to detail, organization, and communication with varied stakeholders
- Ability to work as a team player with the ability to adapt to changing schedules and assignments
Travel Requirements: "Daily commute to site(s)" maybe not needed.
Physical Requirements & Work Environment: list.
We can incorporate travel and physical under Requirements as additional bullet points.
Why Join Profound Research? (Benefits):
- Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients - the work we do here matters
- Professional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
- Leadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
- Collaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
- Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
- Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization
Also AI note: "We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us."
We could include that as a paragraph after Benefits maybe under a heading? Not allowed heading. Could just add a
after Benefits.
Now construct HTML.
We'll have:
About the role
... (company description + why role exists)
Responsibilities
- ...
...
Qualifications
- Bachelor’s degree and 2 years relevant experience in the life science industry OR
- Associate’s degree with 4 years relevant experience in the life science industry OR
- High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience
- Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Daily commute to site(s)
- Ability to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
- May be required to wear personal protective equipment (PPE) in accordance with facility protocols
- Travel between company sites, meetings, or partner locations may be required
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
But we need to ensure we don't lose any details: Physical Requirements & Work Environment includes: "This role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed May be required to wear personal protective equipment (PPE) in accordance with facility protocols Travel between company sites, meetings, or partner locations may be required Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role"
We should include all those points.
Also Travel Requirements: "Daily commute to site(s)" maybe separate.
Now Skills section:
Skills
- Proficient ability to work independently, plan and prioritize with minimal guidance
- Excellent attention to detail, organization, and communication with varied stakeholders
- Ability to work as a team player with the ability to adapt to changing schedules and assignments
Benefits section:
Benefits
- Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients - the work we do here matters
- Professional Growth: We invest in our people through comprehensive training, certification support
. We must not repeat job title. We must not include boilerplate like cookie/navigation/legal/EEO etc. The posting includes a note about AI tools; that's not boilerplate? It's about hiring process; could be considered substantive? It's about hiring process; maybe we should keep? It's not a standard boilerplate but it's about AI usage. The instruction: Remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. The AI note is not exactly those; it's about hiring process. Might be considered part of posting; but it's not about the job itself. Might be considered boilerplate? It's not EEO. It's about AI tools usage in hiring. Could be considered part of the posting but not essential job description. Safer to keep? The instruction says remove boilerplate, duplicated lines, and application instructions. This is not application instructions; it's about AI tools usage. I'd keep it as a paragraph maybe under Benefits or separate? But there is no heading for that. Could add a paragraph after Benefits? But we shouldn't create new heading. Could add a
after Benefits section. That is allowed as part of the HTML fragment (just extra content). However we need to ensure we only output HTML fragment; we can include multiple sections and paragraphs. Let's extract content. About Profound Research: "Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship. Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues. Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency. Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards." Why this Role Exists: "The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values." We can combine. Responsibilities list: - Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements - Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner - Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills - Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up - Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms. - Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors - Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products - Other duties as assigned Requirements: - Bachelor’s degree and 2 years relevant experience in the life science industry OR - Associate’s degree with 4 years relevant experience in the life science industry OR - High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience - Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role - Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens - Proficient ability to work independently, plan and prioritize with minimal guidance - Excellent attention to detail, organization, and communication with varied stakeholders - Ability to work as a team player with the ability to adapt to changing schedules and assignments Travel Requirements: "Daily commute to site(s)" maybe not needed. Physical Requirements & Work Environment: list. We can incorporate travel and physical under Requirements as additional bullet points. Why Join Profound Research? (Benefits): - Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients - the work we do here matters - Professional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career - Leadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time - Collaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well - Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support - Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization Also AI note: "We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us." We could include that as a paragraph after Benefits maybe under a heading? Not allowed heading. Could just add a
after Benefits. Now construct HTML. We'll have:
About the role
... (company description + why role exists)
Responsibilities
- ... ...
Qualifications
- Bachelor’s degree and 2 years relevant experience in the life science industry OR
- Associate’s degree with 4 years relevant experience in the life science industry OR
- High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience
- Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Daily commute to site(s)
- Ability to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
- May be required to wear personal protective equipment (PPE) in accordance with facility protocols
- Travel between company sites, meetings, or partner locations may be required
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
Skills
- Proficient ability to work independently, plan and prioritize with minimal guidance
- Excellent attention to detail, organization, and communication with varied stakeholders
- Ability to work as a team player with the ability to adapt to changing schedules and assignments
Benefits
- Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients - the work we do here matters
- Professional Growth: We invest in our people through comprehensive training, certification support