Associate Director, Clinical Scientist, Ophthalmology
or drop it. So we can include location in a paragraph. Then "Discover Your Role" heading then bullet list of responsibilities. Let's extract responsibilities: - May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical Scientist - Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments - Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape - Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature - Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support - Contributes to planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators - Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies - Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program These are responsibilities. Then "This role requires:" bullet list: - Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc) - 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Ophthalmology - Proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills - Experience in all aspects of conducting global clinical trials and execution of clinical programs - We need an individual who is a strong team-player; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally These are qualifications/requirements/skills. Then "Does this sound like you? Apply now to take your first step towards living the Regeneron Way!" is call to action, we should remove application instructions. Then EEO boilerplate etc remove. Then "Where required, we will provide reasonable accommodation..." remove. Then "Where necessary, we disclose salary ranges for roles in all countries in which we operate." etc. Then "Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits." That's benefits. Then "For additional information about Regeneron benefits in the U.S., please visit ..." remove. Then "If you have any questions, please speak with your recruiter." remove. Then "Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location." remove. Then "As part of the recruitment process, certain background checks may be conducted..." remove. Then "For jobs in Canada: this posting is for an existing position. Salary Range (annually) $176,100.00 - $287,300.00" That's pay info. Thus we have sections: About the role (intro paragraph), Responsibilities (list), Requirements/Qualifications/Skills (maybe combine), Benefits (list), Pay (salary range). Schedule not present, so omit. We need to decide headings: Use
for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). We can choose appropriate headings based on content.
We have About the role: we can put intro paragraph.
Responsibilities: list.
Requirements: maybe combine degree, experience, knowledge, etc. Could be "Requirements". Skills: maybe the team-player etc. But we can combine into Requirements and Skills if needed. However instruction: Prefer a few substantive sections over many thin ones. So we could have About the role, Responsibilities, Requirements (including qualifications and skills), Benefits, Pay.
Thus headings: About the role, Responsibilities, Requirements, Benefits, Pay.
Now we need to output HTML fragment only, no /. Use for each heading, then content:
for prose,
- for lists.
We need to preserve all substantive information, not invent or summarize away detail. Must not omit any substantive info.
Let's extract exact text for each piece.
About the role paragraph: The first paragraph up to "patients worldwide." Let's copy exactly:
"Build Our Future Together At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting Ophthalmology. In this role, you will contribute to the development, evaluation, planning and execution of Internal Medicine clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Work in a matrix environment as part of a cross-functional team (with internal and external vendor representation) and may contribute to candidate development projects through early and/or late phase development. You will report to the Sr Dir/Director, Clinical Science, Internal Medicine and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide."
Note there is a minor grammar issue "ensures" but we keep as is.
Location: "When & Where Location: Tarrytown, NY, Warren, NJ, Cambridge, MA". We could include as a short paragraph after About the role maybe as part of About the role? But location is metadata; we can include as a paragraph.
But we must not repeat job title as heading; we already didn't.
Now Responsibilities list: need to capture each bullet exactly as in posting.
Let's copy each bullet:
- May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical Scientist
- Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments
- Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape
- Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature
- Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support
- Contributes to planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators
- Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies
- Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program
Check punctuation: some have semicolons etc. Keep as is.
Now Requirements: combine degree, experience, knowledge, global trials, team-player etc.
Let's list:
- Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc)
- 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Ophthalmology
- Proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills
- Experience in all aspects of conducting global clinical trials and execution of clinical programs
- We need an individual who is a strong team-player; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally
Note the last bullet is a sentence; we keep.
Now Benefits: list from paragraph:
"Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits."
We can turn into list items.
Now Pay: salary range: "$176,100.00 - $287,300.00" annually. Also note "For jobs in Canada: this posting is for an existing position. Salary Range (annually) $176,100.00 - $287,300.00". So we include that.
We should not include extra fluff like "For jobs in Canada: this posting is for an existing position." That's metadata but maybe we can keep as part of pay paragraph? It's substantive? It's about the posting being for an existing position in Canada. Might be considered minor metadata; we could drop it. But the instruction says preserve ALL substantive information; do NOT invent or summarize away detail. The line "For jobs in Canada: this posting is for an existing position." is substantive? It's about the posting being for an existing position in Canada. Might be considered metadata but it's specific. However we could include it in a short paragraph under Pay.
But we also have location paragraph earlier.
We need to avoid boilerplate like EEO etc. That's fine.
Now construct HTML.
We'll have:
About the role
Build Our Future Together At Regeneron, we