- AbbVie (Durham, NC)
- …focused on the feasibility of AbbVie's clinical trials at the program, study , country and site levels. Drives Analytics innovation and experimentation to ... is a key role to enable application of advanced analytics techniques across clinical development processes, specifically...conducting and delivering fit for purpose analysis related to clinical trial feasibility including, study design, … more
- Lilly (IN)
- …in the study planning, execution, and close out activities of clinical studies . + Proactively identifies potential technical and operational issues/risks and ... Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data Management Associate to deliver study database per business need… more
- BeiGene (San Mateo, CA)
- **General Description:** The Associate Director R&D Quality Excellence, Analytics , and Innovation is responsible for supporting and maintaining a proactive, ... critical role in supporting innovation/modernization and driving change including analytics education/development, process modernization and increasing productivity with innovative… more
- IQVIA (Raleigh, NC)
- …is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and ... Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams...team and/or sub-team. * Accountable for assigned portion of clinical studies as per the contract while… more
- IQVIA (Durham, NC)
- …other required study documentation. * Act as a mentor for clinical staff including conducting co-monitoring and training visits. * Collaborate and liaise with ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...clients. IQVIA is a leading global provider of advanced analytics , technology solutions and clinical research services… more
- IQVIA (Durham, NC)
- IQVIA MedTech is seeking a Clinical Research Associate II with Medical Device monitoring experience! Central Nervous System (CNS) experience is a plus! Job ... Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study … more
- IQVIA (San Diego, CA)
- …coworkers, managers, and clients. IQVIA is a leading global provider of advanced analytics , technology solutions and clinical research services to the life ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,… more
- Walmart (Bentonville, AR)
- Position Summary What you'll do The Director of Healthcare Research Analytics will be responsible for leading data management and analysis of large, real-world ... work collaboratively with cross-functional teams and shape the future of our analytics capabilities. This position will report to the Senior Director, Healthcare… more
- Amgen (South San Francisco, CA)
- …worldwide. It's time for a career you can be proud of. **Scientific Associate Director - Clinical Pharmacology, Modeling & Simulation** **Live** **What you ... innovative modeling methods including mechanistic modeling, data science and predictive analytics to support drug development. The Scientific Associate Director… more
- IQVIA (Radford, VA)
- …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines *… more
- IQVIA (Parsippany, NJ)
- IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines +… more
- University of Utah (Salt Lake City, UT)
- …The data engineering intern supports pieces of our work that involve clinical analytics (eg, patient segmentation, episode prediction, and health outcome ... **Shift** Day **Work Schedule Summary** **Is this a work study job?** No **VP Area** U of U Health...findings, are also important. The intern reports to the Associate Director of Data & Analytics . **This… more
- BeiGene (San Mateo, CA)
- …TA, indication, program levels + Partners with internal stakeholders including global clinical program leaders, global clinical study managers, development ... and risk assessment with therapeutic knowledge balanced with data analytics and interpretation. The Global Strategic Feasibility supports the...across study teams and programs to accelerate study execution. + Partners with global clinical … more
- IQVIA (Durham, NC)
- **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will ... initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.… more
- University of Florida (Jacksonville, FL)
- Clinical Psychologist - Clinical Assistant/ Associate Professor Apply now ... the availability of a full-time faculty position for a Licensed Clinical Psychologist (#00019699). The Clinical Psychologist will provide comprehensive… more
- RELX INC (Dayton, OH)
- …and visualizing data across the Interfolio ecosystem. You will work with the associate director of product and VP of product to determine the roadmap for ... prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate… more
- IQVIA (San Diego, CA)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. +… more
- IQVIA (Durham, NC)
- …+ Global submissions experience IQVIA is a leading global provider of advanced analytics , technology solutions and clinical research services to the life ... au niveau mondial Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects… more
- IQVIA (Overland Park, KS)
- …and join our team. \#CRASDAJD IQVIA is a leading global provider of advanced analytics , technology solutions and clinical research services to the life sciences ... regular lines of communication plus administering protocol and related study training to assigned sites + Evaluating the quality...will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A… more
- IQVIA (Overland Park, KS)
- …and join our team** . IQVIA is a leading global provider of advanced analytics , technology solutions and clinical research services to the life sciences ... plan + Establishing regular lines of communication plus administering protocol and related study training to assigned sites + Evaluating the quality and integrity of… more