Senior Clinical Pharmacology Reporting Specialist
ABBVIE
AbbVie in North Chicago, IL is seeking a Senior Associate in Clinical Pharmacology Scientific Support & Reporting Writing to prepare reports and protocols for clinical trials. The role involves multi-tasking across Phase 1 planning, data analysis, and presentation of results while ensuring regulatory and IQS compliance. You will work under limited supervision to maintain scientific integrity, mentor staff, and collaborate with therapeutic-area teams to drive project timelines and quality #J-18808-Ljbffr ABBVIE
$96.5k - $183.5k
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing Full-time Salary Min: 96500 Salary Max: 183500 Workday Global Grade: 17 Compensation: USD 96500 - USD 183500 - yearly About AbbVie AbbVie's mission is to discover and deliver innovative medicines...SeniorFull timeTemporary work- ...YouTube. Job Description To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking. Responsibilities Prepare...SeniorFull timeTemporary workLocal area
- ...Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical Pharmacology and... ...strategy. Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports,...Senior
$86.7k - $173.3k
...serve people in more than 160 countries.Senior Specialist PricingWorking at AbbottAt Abbott, you... ...are used in hospitals, laboratories, and clinics around the globe. The crucial... ...current business needs.Accountability/Scope:Reports to Manager of Contract & PricingCollaborates...SeniorPermanent employmentContract workTemporary work- AbbVie seeks a lead PK scientist to conceive and execute novel pharmacology research, generating PK/PD proposals and advancing methods for clinical pharmacology programs. The role requires leadership in PK/PD insights and integration with CPPM goals across trial phases...Senior
- AbbVie seeks a lead PK scientist to conceive and execute novel clinical pharmacology research, generating PK/PD proposals and guiding regulatory submissions. You will assess methods, lead modeling efforts, and help translate advances into development programs. You will...Senior
- AbbVie is seeking a senior Clinical Pharmacology Scientist to drive PK/PD strategy across Phase 1-4 programs and lead methodological advances in pharmacometrics. You will partner with cross-functional teams to craft regulatory submissions and scientific publications. The...Senior
- AbbVie seeks a Senior Clinical Pharmacologist (Specialty) to lead pharmacology strategy for clinical development. The role involves designing Phase 1-4 studies, contributing to regulatory submissions, and modeling PK/PD with translational aims. You will collaborate across...Senior
- AbbVie's North Chicago, IL site seeks a senior Clinical Pharmacology leader to conceive and execute novel PK/PD research, lead method development, and drive CPPM goals across discovery and development. You will steer regulatory science and contribute to program strategy...Senior
- ...Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical Pharmacology and... .... Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports,...SeniorFull timeLocal area
- ...Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical Pharmacology and... .... Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports,...SeniorFull timeLocal area
- ...manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that... ...documents including protocols, study reports, population PK reports, exposure-... ...accountability when delegated to by others Senior Clinical Pharmacologist: PhD with 0...SeniorFull timeLocal area
- ...processes (e.g. RFPs, RFIs) Lead in-person fact-based contract negotiations Procurement approval of up to $1,000,000 Prepare analytical reports and dashboards to influence stakeholders without authority Assess complex problems and proposes practical solutions Perform value...SeniorContract work
$84.5k - $162k
Senior Specialist, Business Enablement, Value Generation & Optimization Full-time Salary Min: 84500 Salary Max: 162000 Workday Global... ...applysuppliernegotiationskills Create and maintain dashboards, reporting tools, and program documentation to ensure accurate, timely...SeniorFull timeTemporary work- ...Job Description Purpose: Oversee the production of Lab Samples Operations (LSO) deliverables and timelines for assigned clinical trials. Oversee LSO-related cross-functional meetings for assigned clinical trials. Coordinate discrepancy resolution efforts...SeniorFull timeTemporary workLocal area
- ...PK and toxicology leads, regulatory and clinical development leads as well as medical affairs... ...Understanding and application of the pharmacology, chemistry and non-clinical toxicology... ...responsibility for leading the strategy for periodic reports (DSURs, PSURs, PADERs etc.) Responsible...Senior
$69k - $103k
...A leading packaging company in Waukegan, Illinois, seeks a Senior Staff Accountant to handle a variety of transactional accounting and reporting functions. This full-time role requires a degree in Accounting or Finance and 3+ years of experience in staff accounting. Responsibilities...SeniorFull time- ...comprehensive data management expertise to Clinical Data Management (CDM) team to provide... ...simultaneously Provide updates directly to senior stakeholders as requested by line management... ...status updates for the project Track and report quality and performance metrics and KPIs...Work at office
- ...support as assigned within a defined scope to include managers, clinical research nurse coordinators (CRNC), investigators and sub-... ...throughout the study. Evaluate adverse events and manage safety reporting activities in a timely manner. Review protocols and informed consent...SeniorFull timeTemporary workTraineeshipWork experience placementLocal area
- ...Job Description The Customer Service Specialist is responsible for supporting domestic top... ...recognition, document management, and reporting for various order types: EDI, fax, email... ...control drugs, serialized products, and clinical trials. Research/resolve shipping, ASN/DSCSA...SeniorFull timeTemporary workWork at officeLocal area
- AbbVie is seeking a Senior Scientist in Process Chemistry to lead chemical process research and development from preclinical stages through early clinical phases. You will design and optimize scalable synthetic routes for small molecules, conjugates, and related modalities...Senior
$124.5k - $236.5k
Senior Manager, Clinical Quality Assurance - Americas Full-time Salary Min: 124500 Salary Max: 236500 Workday Global Grade: 19 Compensation... ...thereby advancing the pipeline. This position will report to RDQA Associate Director or RDQA Global Director, AREA Major...SeniorFull timeLocal area- AbbVie is seeking a Senior Analyst for Clinical Photography and Imaging in a Hybrid role in the US. The position supports data science delivery for clinical trials within AbbVie's Data Science team, ensuring protocol requirements are translated into robust clinical systems...Senior
- ..., biology, pharmaceutical sciences, and clinical development. Purpose: The Molecular... ...stakeholders, and contribute to study reports and publications. · Provide experimental... ...Qualifications PhD in neuroscience, pharmacology, biomedical engineering, or a related discipline...SeniorFull timeLocal area
- AbbVie Data Science is seeking a senior program lead to coordinate CDSO study teams and align them with program and study strategies.... ...against program objectives. This role requires 8+ years in pharma/clinical data and strong leadership, communication, and analytical...Senior
- AbbVie is seeking a highly motivated Senior Scientist in Process Chemistry to invent and optimize chemical processes for API development, supporting pre-clinical through early clinical candidates. You will design scalable routes for small molecules, conjugates, and related...Senior
- ...Irvine, CA and San Francisco, CA Position Purpose The Senior Manager, Clinical Product Supply Quality Assurance provides strategic quality... ...and direction for complex investigations, exception reports, deviations, and product quality actions, including high-impact...SeniorFull timeLocal area
- A leading biopharmaceutical company in North Chicago is seeking an Associate Medical Director/Medical Director to oversee clinical development programs in oncology. The candidate must have an M.D. or D.O. and clinical trial experience. Responsibilities include managing...Senior
- ...throughout the study. The position requires an Associate Degree in Nursing (Baccalaureate preferred) with 5+ years of nursing or 4+ years in a clinical research setting, and involves training staff and coordinating protocol activities in compliance with #J-18808-Ljbffr ABBVIESenior
- AbbVie in North Chicago, IL invites an experienced Senior Manager, Clinical Product Supply Quality Assurance to shape program strategy and ensure high-quality, compliant clinical supplies across drug substance, drug product, and finished product stages. You will partner...Senior
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