Associate I, Clinical Pharmacology Scientific Support & Reporting
BioSpace
Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews. Responsibilities Prepare scientific reports and presentations related to clinical trials using available software and templates. Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols. Comply with procedures set forth in relevant IQS documents and Study protocols Comply with the directives issued by the management regarding clinical studies. Commit to producing work of the highest quality Pay close attention to detail Perform literature and competitive intelligence searches Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision. Qualifications Bachelor’s degree, in Science, related to Field with +2 years’ experience in pharmaceutical industry. Or Masters degree in pharmacology or related field. Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally considered. Must possess good oral and written communication skills Ability to use computer to generate reports, analyze data, and create presentations Previous experience may be narrowly-focused or limited. Ability to identify opportunities and participate in process improvement initiatives. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: #J-18808-Ljbffr BioSpace
- AbbVie in the United States seeks a specialist to build data and information needed for internal clinical trial documents and scientific reports, supporting blinded efficacy and safety reviews. You will prepare reports, assist in phase 1 study planning and protocols, ensure...Scientific
- ...Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical... ...Contribute to clinical development by supporting Phase 1-4 studies including... ...including protocols, study reports, population PK reports, exposure...ScientificLocal area
- ...conduct basic science studies for the pharmacological evaluation of novel compounds and... ...and will generate high-quality data reports to support the identification and development of... ...individual must be able to read and adapt scientific literature to advance models and...ScientificFull timeTemporary workLocal area
- ...Job TitleClinical Pharmacology Development ManagerAbout... ...communicates multi-disciplinary Clinical Pharmacology... ...technical and scientific aspects along with Clinical... ...protocols, study reports, population PK reports... ...below qualifications:Associate Director, Clinical PharmacologyPhD...Scientific
$156k - $296.5k
...Associate Director/Director Clinical Pharmacology Apply for the Associate Director/Director Clinical... ..., and external peers. Supports strategic planning for... ...goals. Utilizes scientific expertise to interpret data... ...clinical protocols and reports for regulatory filings....ScientificTemporary work- ...Director, Clinical Pharmacology (Oncology) Full-time Workday Global Grade: 22 About AbbVie... ...strategies, goals, and objectives. Utilizes scientific expertise to provide appropriate... ...Reviews clinical protocols and scientific reports for regulatory filings and anticipates...ScientificFull time
- AbbVie seeks a lead PK scientist to conceive and execute novel scientific research in Clinical Pharmacology, generating PK/PD proposals and leading methods development. You’ll evaluate advances and integrate knowledge into CPPM programs, driving pharmacology strategy for...Scientific
$169.22k - $219.99k
...Licensed Pharmacist(Associate Service Chief) - Operations Department... ..., with the exclusion of clinical pharmacy services and the student... ...opportunities, tuition support, and individual development... ...competence, including regulations, pharmacology, therapeutics and age-...Local areaRemote workRelocation package- ...Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical... ...Contribute to clinical development by supporting Phase 1-4 studies including... ...including protocols, study reports, population PK reports, exposure...ScientificFull timeLocal area
$58.66k - $110.5k
...toconductbasic sciencestudiesfor the pharmacological evaluation of novel... ...high-quality datareportsto support the identification and development... .... Qualifications Associate I: Bachelor’s Degree (noadditionalexperience... ...be able to readand adapt scientific literature toadvance models...ScientificFull timeTemporary work- ...Communicates/presents key Clinical Pharmacology information/strategy to senior... ...and external peers. Supports strategic planning for drug... ...goals and objectives. Utilizes scientific expertise to provide appropriate... ...protocols and scientific reports for regulatory filings and...ScientificFull timeLocal area
- ...nonclinical safety models. Act as a scientific subject matter expert for... ...that deal with anatomic and clinical pathology including not only... ...of comprehensive reports correlating these data. Integrate... ...Familiarity with related fields: pharmacology, toxicology and drug...Scientific
- ...across the research and development organization, including clinical trials, patient safety, and global medical affairs. You... ...analyses, and present results, ensuring accuracy and scientific soundness across reports, tables, listings, and figures. #J-18808-Ljbffr AbbVieScientific
- ...R&D) is a global analytical scientific organization responsible for... ...candidate molecules to Late Stage Clinical. We are building a world-... ...Position Description: For the Associate Scientist II position in the... ...of core discipline and support early phase development of New...ScientificFull timeTemporary workLocal area
- ...s candidate synthetic molecules to support various stages of clinical evaluation, from proof of concept to... ...be able to place data in proper scientific context by consulting and citing relevant... ...meetings. Qualifications Associate Scientist I/II – Formulation About...ScientificFull timeTemporary workLocal area
- ...Description 2027 Overview Summer associates will be immersed in AbbVie’s... ...and litigation counsel. Clinical R &D Legal Academy Work... ...and regulatory matters in support of AbbVie’s therapeutic... ...Bachelor’s or graduate degree in a scientific or engineering discipline...ScientificFixed term contractSummer workInternshipSummer internshipWork at officeLocal areaRelocation package
- ...site Board-Certified Veterinary Clinical Pathologist. The successful... ...a passion for bringing his/her scientific skills to the discovery and development... ...for inclusion in pathology reports from regulatory toxicity studies intended to support the development of new...ScientificFull timeContract workLocal area
- ...Senior Clinical Research Coordinator - Gurnee, IL... ...we connect sponsors' scientific ambitions with high-performing... ...complex studies while supporting staff development,... ...CTMS updates, and case report forms Ensure high-quality... ...Bring to the Team ~ Associate’s or Bachelor’s degree...ScientificWork at officeLocal area
- ...YouTube. Job Description AbbVie IR Scientific Computing Solutions is seeking a highly... ...to implement, configure, maintain, and support software and technology solutions across... ...Investigate, troubleshoot, and resolve reported issues, errors, and performance problems...ScientificFull timeTemporary workLocal area
- ...analysis, data review, and report writing for GLP non-clinical and clinical studies. The... ...Safety and Clinical Pharmacology. Key Responsibilities Include... ...of Abbvie assets in support of nonclinical and clinical... ...for regulated analysis and scientific papers for publication Expertise...ScientificTemporary workLocal area
- ...scientists with the goals of supporting patient,... ...Development Sciences, Pre-clinical Safety. Responsibilities... ...and toxicology reports/summaries and utilize... ...degree in toxicology, pharmacology, or related science... ...Understand relevant scientific literature and apply...ScientificFull timeTemporary workWork at officeLocal area
$58.66k - $100.5k
...YouTube. Job Description Associate Shift Technical Engineer (rotating... ...and applies engineering and scientific knowledge, mathematics, and ingenuity to support process troubleshooting and minimize... ...e.g. documents work status and reports to management with appropriate frequency...ScientificFull timeTemporary workFor contractorsLocal areaShift workRotating shift- ...Enterprise-scale biologics portfolio spanning clinical, commercial, and lifecycle stages... ...manufacturing, quality, regulatory, and scientific leadership Mission: Every model you build... ...manufacturing environments. ~ Support both batch and real-time/streaming data...ScientificFull timeTemporary workLocal area
- ...process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through... ...development of key system interfaces Under direct supervision, supports the execution of all processes in support of study startup, conduct...Full timeTemporary workInternshipLocal area
- ...scientist to generate and analyze precise, reliable data under supervision. You will follow established protocols, report variances, and apply core scientific principles while maintaining laboratory equipment and optimizing operations for efficiency. The role emphasizes...Scientific
$50 - $55 per hour
...looking for a highly motivated person to support these developability efforts and early-stage... ...filling, and lyophilization) Communicate scientific findings and development risks through clear presentations and technical reports to cross-functional teams and senior...ScientificContract workRelocationMonday to Friday- ...Embryonic Stem Cell Associate Scientist/Scientist... ...teams to advance our scientific and translational objectives... ...research grade to clinical grade production (suspension... ...clearly in meetings, reports, and cross-functional... ...strategy. Support white paper/manuscript...Scientific
- ...provides statistical expertise to support the research and development organization... ...areas of work may include clinical trials, patient safety, and global... ...Provide expertisetodesign, analysis and reporting of clinical trials or other scientific research studies. Independently...Scientific
$46 - $50 per hour
...collaborative, fast-moving Clinical Program Development... ...your work directly supports clinical trials and patient... .... The Patient Reported Outcomes Manager is responsible... ...'s Degree in a scientific field or equivalent with... ...a scientific field or associate degree with relevant experience...ScientificHourly payContract work- ...planning, execution and interpretation of clinical trials or research activities of a... ...high-quality clinical data supporting overall product scientific and business strategy. Responsibilities... .... Responsible for assessment and reporting of serious adverse events per...Scientific
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