- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Manager , Clinical Drug Supply... manager of multiple small and/or less complex clinical studies for the functional area in supply ... applies to internally sourced studies and/or CRO/Partnered studies . Collaborates and interacts with clinical trial...Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical … more
- BeOne Medicines (San Carlos, CA)
- …for sample collection schedule, sample processing and shipment, etc. + Participate in clinical study team meetings, providing updates and insights related to ... **General Description:** Manage biomarker (central lab) related operational work for clinical trials **Essential Functions of the job:** + Independently manage… more
- Lilly (Indianapolis, IN)
- …will collaborate with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data Manager and other key business partners to deliver ... Clinical Data Associate , Clinical Data Management Associate to deliver study database per business need and before first patient visit + Influence… more
- Merck (Rahway, NJ)
- …operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have ... development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … Clinical Study Lead or Clinical Study Associate Manager . The CSS will support internally sourced studies and studies out-sourced to ... Job Description The ** Clinical Study Specialis** t (CSS) provides...assigned to support the execution of one or more studies across a program. The CSS receives assignments from… more
- Sumitomo Pharma (Nashville, TN)
- …We are currently seeking a versatile and experienced Senior Manager - Associate Director level scientist with strengths in clinical pharmacology, and a ... PK/PD, clinical pharmacology and drug-metabolism expertise to project teams. + Design clinical pharmacology components of clinical studies . + Create … more
- Astrix Technology (Euclid, OH)
- ** Associate Scientist** Clinical Project Manager /Scientist Euclid, OH, US Pay Rate Low: 65000 | Pay Rate High: 75000 + Added - 05/05/2025 Apply for Job **Pay ... $65,000-$75,000** **Position Summary** We are looking for a detail-oriented and proactive Associate Scientist to join our Stability Laboratory. In this role, you… more
- Vanderbilt University Medical Center (Nashville, TN)
- …management of paperwork and administrative tasks/procedures for clinical research studies within the Holowatyj Laboratory. The Associate Program Manager ... & Team with some guidance-such that the integrity and rigorous quality of clinical and translational research is maintained, the study objectives are… more
- IQVIA (New Providence, NJ)
- …This role is aligned with IQVIA's Centralized Outsourcing Operations Hub (COOH) team. The Clinical Training Manager or Associate Director will be responsible ... for the development and implementation of learning programs for clinical -based roles with patients and healthcare providers in both the field-based and virtual… more
- Abbott (Minneapolis, MN)
- …Summary Under the supervision of senior colleague/ manager (or delegate), the Associate Clinical Site Lead drives study execution and operational ... manager (or delegate): Develop and support a productive clinical territory: + Identify, develop, and maintain sites capable...other Abbott clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed.… more
- AdventHealth (Orlando, FL)
- **Program Manager - Study Intake - AdventHealth...for the assessment, review and ultimately the initiation of clinical trials and research studies for a ... outpatients each year **The role you'll contribute:** The Program Manager - Study Intake ( Manager )...assessment and review of research opportunities. o Certification as Clinical Research Associate (CCRA) through the Society… more
- AdventHealth (Orlando, FL)
- …role you'll contribute:** The Study Intake Support Specialist will assist the Study Intake Manager in the startup of Phase I-IV industry-sponsored and ... Intake Support Specialist is immediately accountable to the Study Intake Manager and works with them...cabinet and verify receipt of necessary documents_ + _Enter studies into the Master Study Database and… more
- Kelly Services (St. Louis, MO)
- Kelly Science & Clinical is seeking a skilled, full-time, temporary-to-permanent ** Associate Project Manager ** with experience in data reporting for a client ... + Target Pay Rate: $25-30/hour **Position Overview:** As an Associate Project Manager , you will play a...and regulatory teams with data review, collection, reporting, and clinical studies related to external investigators or… more
- Hartford HealthCare (Hartford, CT)
- …information * Coordinates all aspects of study activity as required of a Clinical Research Associate * This is a grant funded position * Bachelor degree ... us. *Job Summary:* As a specialized research professional the Clinical Research Associate (CRA) collaborates with the...the compliance, financial, personnel and all aspects of the clinical study . *Job Responsibilities:* * Compiles and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …and compliance in all US Medical activities. + Drive and deliver all aspects of clinical study execution from study concept to final reporting, coordinate ... application is true to the best of my knowledge. **Job Description** ** Associate Director, Clinical Research, Value & Evidence Generation, US Medical**… more
- Abbott (Alameda, CA)
- …. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality ... you'll do:** + Conduct single or multi-center medical device clinical studies . + Perform study ...for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed. + Participate… more
- Rush University Medical Center (Chicago, IL)
- …disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago **Req ... Clinical Practice (GCP) S/he will coordinate standard clinical research studies conducted by PI(s) which...serious adverse events). * Work with PI(s), sponsor, compliance, clinical staff and/or manager to identify and… more
- Abbott (Alameda, CA)
- …clinical data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager / Study Lead as needed. + Proactively and ... monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH...effectively communicate the status of clinical studies to management. + Participate in… more
- Abbott (Alameda, CA)
- …clinical data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager / Study Lead as needed. + Proactively and ... monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH...effectively communicate the status of clinical studies to management. + Participate in… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 04, 2025 Requisition # 106218 The ... will not have any impairment. The Stanford ADRC seeks a full-time Clinical Research Coordinator Associate . The desired candidate is self-motivated,… more
Related Job Searches:
Associate,
Associate Manager,
Clinical,
Clinical Associate,
Clinical Manager,
Clinical Manager Associate,
Clinical Study Manager,
Manager,
Study,
Study Manager