Clinical Procedures Jobs in Tonawanda, NY

About This Role:Pharmacometric analyses and insight are critical in the development of drug candidates determination of product viability and maximization of commercial value at Biogen. The Associate Director Pharmacometrics has responsibility for high priority clinical development as More...

Take your career to the next level and be involved in study startup processes in the US. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. HomebasedYou will:Supports all processes critical for site activ More...

Healthcare Talent Support is a premier recruitment agency dedicated to connecting exceptional healthcare talent with outstanding organizations. We understand that the right people make all the difference in providing topquality care and we strive to match highly skilled professionals More...

GENERAL SUMMARY: The College of Nursing seeks dynamic innovative faculty for part time (contributing) positions in the Master of Science in Nursing program.The key responsibilities of the position are to teach advanced pharmacology courses for nurse practitioner students.  & More...

GENERAL SUMMARY: The College of Nursing seeks dynamic innovative faculty for part time (contributing) positions in the Master of Science in Nursing program.The key responsibilities of the position are to teach advanced pharmacology courses for nurse practitioner students.  & More...

The EHR Support Lead is a critical role within Privia responsible for ensuring the optimal performance and utilization of the athenaOne EHR application. This individual will provide leadership and supervision to the EHR Support Team including Platform Associates Senior Platform Specia More...

Description: 100% onsite Oceanside CA Hours: MonFri business hours Reason for opening: continued/extra workload (projects) Role: Senior Research Associate Biologics Drug Product Development (BDPD). Duration: 12 months could possibly extend additional time however that wont be know More...

Drives key innovative and strategic projects and priorities for USMA oncology. Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions; generation of clinical and scientific data More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...

Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training.Departmental Responsibilities: Develop tracking tools for the Study Startup departmentPrepare departmental reportsPlan organise and fo More...

The Associate Scientific/Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health care professional and provider interactions (Payers Patients Prescribers and Providers); generation of clinical and scienti More...

We are currently seeking a highly skilled and detailoriented Product Assessor to join our team. In this position you will be responsible for conducting technical file reviews against the European Medical Device Directive and Medical Device Regulation for Class I/IIa/IIb and/or Class I More...

Job SummaryThe National Account Director GPO Trade and Distribution is responsible for developing and maintaining business relationships with Oncology and Immunology Institutional and Community GPOs and Hospital and Community Immunologists Rheumatologists Endocrinologists and Oncologi More...

Job SummaryThe National Account Director GPO Trade and Distribution is responsible for developing and maintaining business relationships with Oncology and Immunology Institutional and Community GPOs and Hospital and Community Immunologists Rheumatologists Endocrinologists and Oncologi More...

Job SummaryThe National Account Director GPO Trade and Distribution is responsible for developing and maintaining business relationships with Oncology and Immunology Institutional and Community GPOs and Hospital and Community Immunologists Rheumatologists Endocrinologists and Oncologi More...

Description: Job Title: Research Associate III/ Histology Technical Specialist Location: Foster City CA Duration: 11 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Pay Range: Negotiable Essential Duties and Responsibilities O More...