Clinical Research Assistant Jobs in the United States
AbbVie
Charlotte, NC
The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law. 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 ingood faith it will pay for this role at the time of this posting based on the job grade for this position.
AbbVie
Minneapolis, MN
To enable AbbVie s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law.
AbbVie
New York City, NY
The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law. 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 ingood faith it will pay for this role at the time of this posting based on the job grade for this position.
AbbVie
East Irvine, CA
She/He/They will be responsible for managing a diverse team of in vitro/ex vivo scientists to design and perform cellular and complex organ culture studies using existing and novel assays aimed at evaluating novel candidate molecules, performing CRISPR screens for identification of new targets and further validation of mechanism of actions. The ideal candidate will have a strong and established background in pharmacology (in hair a plus), specializing in in vitro assays (biochemical, cellular, complex models) plus novel target screens, and a proven track record of successfully leading diverse project teams to produce novel therapeutics.
AbbVie
North Chicago, IL
The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law. 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 ingood faith it will pay for this role at the time of this posting based on the job grade for this position.
AbbVie
North Chicago, IL
The main function of this position will be to develop and implement LC-MS (liquid chromatography-mass spectrometry)-based bioanalysis and in vitro characterization assays for biologics entities, including monoclonal antibodies, multi-specific antibodies and antibody drug conjugates (ADC), peptides, lipid nanoparticles (LNP), Adeno-Associated Virus (AAV) etc. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law.
AbbVie
San Diego, MA
The main function of this position will be to develop and implement LC-MS (liquid chromatography-mass spectrometry)-based bioanalysis and in vitro characterization assays for biologics entities, including monoclonal antibodies, multi-specific antibodies and antibody drug conjugates (ADC), peptides, lipid nanoparticles (LNP), Adeno-Associated Virus (AAV) etc. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law.
AbbVie
North Chicago, IL
PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Masters Degree or equivalent education and typically 8+ years of experience, Bachelors Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). 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 Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.
AbbVie
North Chicago, IL
PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Masters Degree or equivalent education and typically 8+ years of experience, Bachelors Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). 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 Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.
AbbVie
North Chicago, IL
PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Masters Degree or equivalent education and typically 8+ years of experience, Bachelors Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, Journal club.
AbbVie
South San Francisco, CA
PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Masters Degree or equivalent education and typically 8+ years of experience, Bachelors Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). 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 Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.
AbbVie
South San Francisco, CA
The intern will explore the utility of incorporating preclinical animal PBPK models in benefiting human PK predictions and may execute various other prediction methods including, but not limited to, allometric scaling and in vitro-in vivo extrapolation (IVIVE), to provide a comprehensive evaluation of predictive performance using both internal and external data. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law.
AbbVie
Atlanta, GA
Maintain Cross-Functional Field Partnerships:Creates, maintains, and collaborates in relationships with Cross-Functional partnerships, including, but not limited to: in field commercial teams, engagement with site management and monitoring and clinical research associates, the Therapeutic Area, HEOR, and with the Medical Outcome Science Liaisons. Therapeutic Disease State, Landscape, and Asset Expert:Continually educates self on market issues/trends, product knowledge, and new therapeutic areas of interest as it pertains to specific business responsibilities, including creating awareness and relationships for AbbVie in the Medical community.
Joulé
San Diego, CA
Trains and supports external trial staff regarding requirements for CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability and temperature monitoring, query resolution, essential document collection and ITF filing. You are working for a sponsor, in a therapeutically aligned model supporting Endocrinology studies, conducting remote and onsite monitoring of regional sites in a risk-based monitoring model.
Joulé
Dallas, TX
Trains and supports external trial staff regarding requirements for CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability and temperature monitoring, query resolution, essential document collection and ITF filing. You are working for a sponsor, in a therapeutically aligned model supporting Endocrinology studies, conducting remote and onsite monitoring of regional sites in a risk-based monitoring model.
Joulé
Carnegie, PA
Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes. A top-ranked research university is currently searching for a Clinical Research Coordinator for one of its growing departments to be responsible for assisting in the operations of ongoing clinical trials.
Joulé
Asheville, NC
Duties and Responsibilities: Duties include but are not limited to: • Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements . • Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications .
Joulé
Nashville, TN
Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications . Duties and Responsibilities: Duties include but are not limited to: • Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements .