Associate I, Clinical Pharmacology Scientific Support & Reporting
$65.5k - $125.5kSmartRecruiters, Inc.
Associate I, Clinical Pharmacology Scientific Support & Reporting Full-time Salary Min: 65500 Salary Max: 125500 Workday Global Grade: 14 Compensation: USD 65,500 - USD 125,500 - yearly 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. 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 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. 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. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal 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 determinate. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employer 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. #J-18808-Ljbffr SmartRecruiters, Inc.
$65.5k - $125.5k
...information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded... ...pharmaceutical industry. Or Masters degree in pharmacology or related field. Associates degree/RN with 6+ years of experience in pharmaceutical...ScientificTemporary workWork at officeImmediate startRemote workMonday to Friday- ...Associate-level position supporting clinical pharmacology operations by preparing scientific reports, analyzing trial data, and assisting with study planning documents. Requires bachelor's degree in science with pharmaceutical industry experience, or master's in pharmacology...Scientific
- ...Associate role supporting clinical pharmacology operations at a pharmaceutical company. Responsibilities include preparing scientific reports, analyzing clinical trial data, and drafting phase 1 study protocols while ensuring compliance with internal procedures and regulatory...Scientific
- AbbVie is seeking an Associate I in Clinical Pharmacology Scientific Support & Reporting in Illinois. You will prepare reports for clinical trials, assist with Phase 1 documents, and ensure compliance with study protocols and IQS guidelines. The role requires 2+ years in...Scientific
- ...Senior Clinical Pharmacologist position at AbbVie focused... ...executing clinical pharmacology research and... ...cross-functional teams to support drug development from... ...including protocols, study reports, population PK analyses... ...response evaluation Lead scientific presentations and...Scientific
$109.5k - $208.5k
...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...ScientificWork at officeLocal areaImmediate startRemote workMonday to Friday- ...seeks a lead PK scientist to conceive and execute novel scientific research in Clinical Pharmacology that advances CPPM goals. You will generate PK/PD... ...integrate knowledge into programs. The role includes supporting Phase 1-4 studies, authoring regulatory documents, and...Scientific
- ...scientist to conceive and execute innovative pharmacology research within CPPM. You will generate... ...programs. The role requires heading-up clinical pharmacology activities across Phase 1-... .... AbbVie emphasizes collaboration and scientific leadership. #J-18808-Ljbffr AbbVieScientific
$40 - $50 per hour
Job Title: Clinical Application Specialist II Data Analytics... ...II Data Analytics supports the Global... ...Periodic Safety Update Reports (PSURs), and Briefing... ...analytical outputs align with scientific, clinical, and regulatory... ...areas and their associated epidemiology. Ability...ScientificContract workTemporary workRemote work- AbbVie seeks a Senior Clinical Pharmacologist (Specialty) to lead pharmacology strategy for clinical development. The role involves designing Phase 1-4 studies... ...groups, publish findings, and present at scientific conferences. Ideal candidates hold a PhD or PharmD...Scientific
- AbbVie is seeking a senior leader in Clinical Pharmacology to guide drug development strategies and communicate scientific insights to senior management and regulators. You will lead PK/PD activities across major projects, liaise with R&D, Regulatory, and cross-functional...Scientific
- ...Director of Clinical Pharmacology at AbbVie leads pharmacokinetic and pharmacodynamic activities... ...coordination, and potential team management to support R&D objectives. Responsibilities... ...R&D, regulatory, and management on scientific strategy, critical decisions, and...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
- ...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
- ...communicates multi-disciplinary Clinical Pharmacology development plans and... ...critically evaluating technical and scientific aspects along with Clinical... ...including protocols, study reports, population PK reports,... ...below qualifications: Associate Director, Clinical...ScientificFull timeLocal area
$88k - $136k
...coupling upon drug binding, supporting a pipeline of first-in-class... ...is for an in vitro/in vivo Associate Scientist reporting to the Senior Director of Pharmacology. We seek an enthusiastic, collaborative... ...individual with strong scientific rigor and excellent...ScientificFull timeRelocation packageFlexible hours- ...The assignment lasts 12 months and involves collaboration across cross-functional teams to design, analyze, and report results from clinical trials or scientific studies. The role requires advanced statistics training (PhD in Statistics with 1-3 years, or MS with 5-7...ScientificRemote job
- ...Description Communicates/presents key Clinical Pharmacology information/strategy to senior and... ...strategies, goals, and objectives. Utilizes scientific expertise to provide appropriate... ...Reviews clinical protocols and scientific reports for regulatory filings and anticipates...ScientificFull timeLocal area
$80k - $95k
...Executive for our Science & Clinical staffing division! We’re... ...representatives from relevant business associations (e.g., Society of Human... ...'s degree preferred; Scientific, Life Science, Healthcare degree... ...? \n Kelly takes pride in supporting the whole person, their...ScientificImmediate startRemote workWork from home$35 - $50 per hour
...of Travere as we continue to grow in support of our commitment to identify, develop... ...to senior leadership. \n \n The Clinical Pharmacology Intern will contribute to a focused Pharmacology... ...data summaries that communicate scientific findings. \n Conduct literature...ScientificHourly payTemporary workSummer workInternshipRemote work3 days per week- ...Executive Medical Director leading clinical development programs in solid tumor oncology... ...analyze, and interpret protocols, study reports, and regulatory submissions Coordinate... ...timeline delivery May supervise Medical and Scientific Directors and serve on Clinical Strategy...Scientific
- ...AbbVie seeks a Manager to lead Clinical Outcome Assessment licensing,... ..., and team management to support clinical development initiatives... ..., manage, and develop direct reports while building institutional... ...Requirements Bachelor's degree in scientific field or equivalent relevant...Scientific
- ...Senior Medical Director overseeing hematology clinical development programs at a pharmaceutical company. Directs trial... ...accumulating safety and efficacy data Develop scientific content for protocols, study reports, and regulatory submissions Assess and report serious...Scientific
- ...Abbott seeks a Senior Clinical Laboratory Auditor to lead quality system audits across clinical... ..., risk assessment, and executive reporting. Responsibilities Direct, plan, and... ...Bachelor's degree or equivalent experience in scientific field Lead auditor certificate for...Scientific
$160.5k - $305k
...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- ...Senior Scientific Director position overseeing clinical development programs in oncology, specifically non-Hodgkin lymphoma and leukemia. Leads cross-functional... ...protocol development, analysis, interpretation, and reporting of scientific content and regulatory submissions...Scientific
- ...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...ScientificFull timeLocal area
$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- ...is searching for an in-house Associate General Counsel for our IP Due... ...legal team. This position will support AbbVie's business development... ...clear, actionable due diligence reports and risk assessments to senior legal, business, and scientific stakeholders Partner with...Scientific3 days per week
- ...program is to develop and support high-potential... ...functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance... ...enter the program as Associate Medical Directors.... ...strong medical and scientific principles, knowledge... ...safety monitoring reports to regulatory...ScientificRotational programFull timeTemporary workLocal area
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