Principal Scientist

We need to output HTML fragment only, with headings

for sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. Remove boilerplate, navigation, legal, EEO, etc. Also remove duplicated lines, application instructions. Keep all substantive info. Let's parse the posting. Content: - Regeneron's Bioanalytical Sciences group, located in Tarrytown, NY, is looking for a Principal Scientist. - In this role you will serve as the Bioanalytical Sciences Lead to manage bioanalytical strategy and oversee bioanalytical activities for clinical programs. - Acts as the liaison between Bioanalytical Sciences (BAS) and clinical study teams to effectively manage pharmacokinetics (PK), immunogenicity, and biomarker deliverables and timelines for clinical studies. - Supports regulatory submissions and interactions to ensure the completeness of sections related to immunogenicity and bioanalysis of PK and target biomarker samples. - When & Where Location: Tarrytown, NY - Work model/flexibility: 4 days onsite - Discover Your Role (maybe heading) - Serve as the Bioanalytical Sciences Lead on clinical study teams and participates on project teams both internal and external to Regeneron to oversee bioanalysis for clinical studies. - Contributes to the development and management of bioanalytical strategy including immunogenicity risk assessment, assay selection, and sampling timepoints for clinical programs. - Act as a liaison between Bioanalytical Sciences (BAS) and the clinical development team, work closely with groups within BAS, as well as the Clinical Pharmacology group, Regulatory Affairs, clinical study teams, and other working groups to establish bioanalytical deliverables and timelines for multiple projects. - Review sample analysis documentation and clinical sample analysis reports. - Contribute to regulatory submissions and responses to regulatory inquiries. - Contribute to and review clinical study-related documents including expanded synopses, protocols, amendments, statistical analysis plan, and clinical study reports. - Review data, SOPs, publications, and guidelines to ensure the conduct of bioanalysis is compliant with industry practice and/or regulatory expectations. - Prepare and present scientific data at internal and external meetings. - This Role Requires PhD or BS/MS with 5+ years of experience in immunology, pharmaceutical sciences, or related field. - Experience with bioanalytical techniques, e.g., ELISA, ECL (MSD), LC-MS, PCR, flow cytometry, or immunogenicity assays. - Experience with writing/reviewing scientific documents, reports, and contributing to regulatory submissions. - Strong communication, project management, and interpersonal skills. - Does this sound like you? Apply now to take your first step towards living the Regeneron Way! (application instruction - remove) - We are committed to building a workplace with an inclusive culture. (EEO boilerplate - remove) - Regeneron is an equal opportunity employer... (remove) - Where required, we will provide reasonable accommodation... (remove) - Where necessary, we disclose salary ranges for roles in all countries... (maybe part of Pay? but we have specific salary range later) - The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. (Pay info) - In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. (maybe not needed) - 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. (Benefits) - For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. (link maybe keep? but it's more info; we can keep as part of Benefits) - For other locations, additional information will be provided during the recruitment process. (maybe not needed) - If you have any questions, please speak with your recruiter. (application instruction - remove) - 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. (maybe schedule? but we have work model/flexibility: 4 days onsite) - As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. (boilerplate - remove) - For jobs in Canada: this posting is for an existing position. Salary Range (annually) $128,600.00 - $210,000.00. (Pay info) We need to include sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide what content goes where. About the role: maybe a brief overview: Regeneron's Bioanalytical Sciences group, located in Tarrytown, NY, is looking for a Principal Scientist. In this role you will serve as the Bioanalytical Sciences Lead to manage bioanalytical strategy and oversee bioanalytical activities for clinical programs. Acts as the liaison between Bioanalytical Sciences (BAS) and clinical study teams to effectively manage pharmacokinetics (PK), immunogenicity, and biomarker deliverables and timelines for clinical studies. Supports regulatory submissions and interactions to ensure the completeness of sections related to immunogenicity and bioanalysis of PK and target biomarker samples. Responsibilities: list of duties: Serve as the Bioanalytical Sciences Lead on clinical study teams and participates on project teams both internal and external to Regeneron to oversee bioanalysis for clinical studies. Contributes to the development and management of bioanalytical strategy including immunogenicity risk assessment, assay selection, and sampling timepoints for clinical programs. Act as a liaison between Bioanalytical Sciences (BAS) and the clinical development team, work closely with groups within BAS, as well as the Clinical Pharmacology group, Regulatory Affairs, clinical study teams, and other working groups to establish bioanalytical deliverables and timelines for multiple projects. Review sample analysis documentation and clinical sample analysis reports. Contribute to regulatory submissions and responses to regulatory inquiries. Contribute to and review clinical study-related documents including expanded synopses, protocols, amendments, statistical analysis plan, and clinical study reports. Review data, SOPs, publications, and guidelines to ensure the conduct of bioanalysis is compliant with industry practice and/or regulatory expectations. Prepare and present scientific data at internal and external meetings. Requirements: maybe education/experience: PhD or BS/MS with 5+ years of experience in immunology, pharmaceutical sciences, or related field. Experience with bioanalytical techniques, e.g., ELISA, ECL (MSD), LC-MS, PCR, flow cytometry, or immunogenicity assays. Experience with writing/reviewing scientific documents, reports, and contributing to regulatory submissions. Qualifications: maybe similar to requirements? Could combine but we need separate sections if content distinct. Could treat Requirements as education/experience, Qualifications as specific technical skills? But we have Skills section for soft skills. Let's map: - Requirements: PhD or BS/MS with 5+ years of experience in immunology, pharmaceutical sciences, or related field. - Qualifications: Experience with bioanalytical techniques, e.g., ELISA, ECL (MSD), LC-MS, PCR, flow cytometry, or immunogenicity assays. Experience with writing/reviewing scientific documents, reports, and contributing to regulatory submissions. - Skills: Strong communication, project management, and interpersonal skills. Benefits: 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. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. (maybe keep link as part of benefits) Pay: Salary Range (annually) $128,600.00 - $210,000.00. Also mention final offer determined within range based on country, role level, skills and experience. Could include that. Schedule: Work model/flexibility: 4 days onsite. Also location: Tarrytown, NY. Could include location in About the role or Schedule? Schedule section could include work model and location. We must not repeat job title as heading. Already not. We must not include boilerplate like EEO, accommodation, etc. We must not include application instructions like "Apply now", "If you have any questions, please speak with your recruiter", etc. We must not include duplicated lines. We must preserve all substantive information. Now produce HTML fragment with

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      with location and work model. Let's craft. About the role: could be

      summarizing. Now check for any duplicated content: The initial paragraph about role appears again in Discover Your Role section; we need to avoid duplication. We'll combine unique content. Let's extract unique substantive sentences: From first paragraph: - Regeneron's Bioanalytical Sciences group, located in Tarrytown, NY, is looking for a Principal Scientist. - In this role you will serve as the Bioanalytical Sciences Lead to manage bioanalytical strategy and oversee bioanalytical activities for clinical programs. - Acts as the liaison between Bioanalytical Sciences (BAS) and clinical study teams to effectively manage pharmacokinetics (PK), immunogenicity, and biomarker deliverables and timelines for clinical studies. - Supports regulatory submissions and interactions to ensure the completeness of sections related to immunogenicity and bioanalysis of PK and target biomarker samples. From Discover Your Role bullet points (some overlapping): - Serve as the Bioanalytical Sciences Lead on clinical study teams and participates on project teams both internal and external to Regeneron to oversee bioanalysis for clinical studies. (similar to first bullet) - Contributes to the development and management of bioanalytical strategy including immunogenicity risk assessment, assay selection, and sampling timepoints for clinical programs. - Act as a liaison between Bioanalytical Sciences (BAS) and the clinical development team, work closely with groups within BAS, as well as the Clinical Pharmacology group, Regulatory Affairs, clinical study teams, and other working groups to establish bioanalytical deliverables and timelines for multiple projects. (similar to liaison) - Review sample analysis documentation and clinical sample analysis reports. - Contribute to regulatory submissions and responses to regulatory inquiries. - Contribute to and review clinical study-related documents including expanded synopses, protocols, amendments, statistical analysis plan, and clinical study reports. - Review data, SOPs, publications, and guidelines to ensure the conduct of bioanalysis is compliant with industry practice and/or regulatory expectations. - Prepare and present scientific data at internal and external meetings. We can combine responsibilities list from these, avoiding duplicates. Now requirements/qualifications/skills: - This Role Requires PhD or BS/MS with 5+ years of experience in immunology, pharmaceutical sciences, or related field. - Experience with bioanalytical techniques, e.g., ELISA, ECL (MSD), LC-MS, PCR, flow cytometry, or immunogenicity assays. - Experience with writing/reviewing scientific documents, reports, and contributing to regulatory submissions. - Strong communication, project management, and interpersonal skills. We can