Eli Lilly and Company
Advisor/Sr. Advisor - Clinical Research Scientist - Neuroscience Clinical Develo
Eli Lilly and Company, Indiana, Pennsylvania, us, 15705
Overview
Advisor/Sr. Advisor - Clinical Research Scientist – Neuroscience Clinical Development: Neuropsychologist. Pay: $142,500.00/yr - $228,800.00/yr. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. We’re looking for people who are determined to make life better for people around the world. Base pay range provided in the job post. This role supports the Neuroscience medical development team in the development, conduct, and reporting of clinical trials in support of product registration and commercialization, as well as global clinical trial implementation and regulatory interactions. Purpose Through scientific and medical training, clinical expertise, and relevant clinical experience, the Clinical Research Scientist – Clinical Development: Neuropsychologist contributes to protocol design, study reports, publications and data dissemination, product pricing and access materials, regulatory interactions, and external medical outreach. The role ensures activities comply with applicable regulations and company policies, including GCPs and integrity standards. Responsibilities
Overall Responsibilities The Clinical Research Scientist provides scientific support for clinical trials across the Neuroscience platform and serves patients with neurological and psychiatric conditions. Acts as a scientific resource for study teams on endpoint selection, central monitoring strategies, and translation of trial outcomes into meaningful benefits. Design and execution support for phase 2/3 studies aligned with commercial needs. Specific Responsibilities Clinical Planning
- Collaborate with regions, Discovery, Program Phase Medicine, and Clinical Pharmacology to develop and maintain a Draft Launch Label and Value Proposition; contribute to clinical strategies and study protocol design. Contribute to global alignment of clinical strategy and plans. Stay updated on pre-clinical and clinical data relevant to the molecule. Clinical Research/Trial/Execution and Support
- Plan and review scientific content of protocols and documents; oversee informed consent; monitor patient safety and participate in global safety reviews; collaborate on local trials and governance; review risk profiles; participate in investigator identification and site initiation activities; ensure regulatory and ethical requirements are met according to GCPs and local laws. Provide training and address investigator questions; support operational teams and investigators; address scientific information needs. Scientific Data Dissemination/Exchange
- Ensure compliance with data dissemination policies; support external engagement with health care professionals; participate in clinical trial registry reporting; plan symposia and meetings; prepare scientific responses; develop collaborations with experts and societies; support publications and training; provide congress support. Regulatory Support
- Participate in label changes and regulatory submissions; provide medical input to regulatory teams; assist with regulatory reports and advisory committee preparation; engage in risk management with GPS and affiliates. Scientific/Technical Expertise and Development
- Critically read literature and stay current with developments; train the study team; act as protocol expert; monitor trends in clinical practice and access; pursue extramural opportunities; participate in scientific events and workshops. General Responsibilities
- Set and meet professional development goals; support budgeting and recruitment efforts; collaborate with partners; provide feedback and participate in committees; maintain training maps and leadership behaviors; represent the Lilly brand and patients in all activities. Qualifications
Basic Requirements
- Doctoral degree (Ph.D., Psy.D. or equivalent) in Clinical Neuropsychology with 2+ years of industry or academic experience post-training; clinical/research experience with adults with neurological/psychiatric disorders; experience conducting assessments and using standardized scales; statistical/psychometric analysis proficiency; publications or conference presentations. Additional Information
Fluent in English (writing and speaking). Ability to travel domestically and internationally as needed. Position location: Indianapolis, IN or Remote. Lilly is dedicated to equal opportunity employment. If accommodations are needed during the application process, please submit the accommodation request form. Lilly is an Equal Employment Opportunity (EEO) employer and does not discriminate on protected characteristics. Our ERGs support diverse employees. Actual compensation depends on education, experience, skills, and location. Anticipated wage: $142,500 - $228,800. Full-time employees may be eligible for a company bonus and comprehensive benefits. #WeAreLilly Seniority level
Mid-Senior level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Lilly.
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Advisor/Sr. Advisor - Clinical Research Scientist – Neuroscience Clinical Development: Neuropsychologist. Pay: $142,500.00/yr - $228,800.00/yr. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. We’re looking for people who are determined to make life better for people around the world. Base pay range provided in the job post. This role supports the Neuroscience medical development team in the development, conduct, and reporting of clinical trials in support of product registration and commercialization, as well as global clinical trial implementation and regulatory interactions. Purpose Through scientific and medical training, clinical expertise, and relevant clinical experience, the Clinical Research Scientist – Clinical Development: Neuropsychologist contributes to protocol design, study reports, publications and data dissemination, product pricing and access materials, regulatory interactions, and external medical outreach. The role ensures activities comply with applicable regulations and company policies, including GCPs and integrity standards. Responsibilities
Overall Responsibilities The Clinical Research Scientist provides scientific support for clinical trials across the Neuroscience platform and serves patients with neurological and psychiatric conditions. Acts as a scientific resource for study teams on endpoint selection, central monitoring strategies, and translation of trial outcomes into meaningful benefits. Design and execution support for phase 2/3 studies aligned with commercial needs. Specific Responsibilities Clinical Planning
- Collaborate with regions, Discovery, Program Phase Medicine, and Clinical Pharmacology to develop and maintain a Draft Launch Label and Value Proposition; contribute to clinical strategies and study protocol design. Contribute to global alignment of clinical strategy and plans. Stay updated on pre-clinical and clinical data relevant to the molecule. Clinical Research/Trial/Execution and Support
- Plan and review scientific content of protocols and documents; oversee informed consent; monitor patient safety and participate in global safety reviews; collaborate on local trials and governance; review risk profiles; participate in investigator identification and site initiation activities; ensure regulatory and ethical requirements are met according to GCPs and local laws. Provide training and address investigator questions; support operational teams and investigators; address scientific information needs. Scientific Data Dissemination/Exchange
- Ensure compliance with data dissemination policies; support external engagement with health care professionals; participate in clinical trial registry reporting; plan symposia and meetings; prepare scientific responses; develop collaborations with experts and societies; support publications and training; provide congress support. Regulatory Support
- Participate in label changes and regulatory submissions; provide medical input to regulatory teams; assist with regulatory reports and advisory committee preparation; engage in risk management with GPS and affiliates. Scientific/Technical Expertise and Development
- Critically read literature and stay current with developments; train the study team; act as protocol expert; monitor trends in clinical practice and access; pursue extramural opportunities; participate in scientific events and workshops. General Responsibilities
- Set and meet professional development goals; support budgeting and recruitment efforts; collaborate with partners; provide feedback and participate in committees; maintain training maps and leadership behaviors; represent the Lilly brand and patients in all activities. Qualifications
Basic Requirements
- Doctoral degree (Ph.D., Psy.D. or equivalent) in Clinical Neuropsychology with 2+ years of industry or academic experience post-training; clinical/research experience with adults with neurological/psychiatric disorders; experience conducting assessments and using standardized scales; statistical/psychometric analysis proficiency; publications or conference presentations. Additional Information
Fluent in English (writing and speaking). Ability to travel domestically and internationally as needed. Position location: Indianapolis, IN or Remote. Lilly is dedicated to equal opportunity employment. If accommodations are needed during the application process, please submit the accommodation request form. Lilly is an Equal Employment Opportunity (EEO) employer and does not discriminate on protected characteristics. Our ERGs support diverse employees. Actual compensation depends on education, experience, skills, and location. Anticipated wage: $142,500 - $228,800. Full-time employees may be eligible for a company bonus and comprehensive benefits. #WeAreLilly Seniority level
Mid-Senior level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Lilly.
#J-18808-Ljbffr