The Associate Director of Clinical Pharmacology will have a key role in advancing our growing pipeline. The ideal candidate will champion the use of clinical pharmacology expertise and model informed drug development (MIDD) strategies to enhance the development of novel therapies across all phases of R&D and therapeutic areas, including neurology, ophthalmology, and rare

Indicate key areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation. Clinical Support Duties 1. Maintains a good professional relationship with outside storage facility, Access Corporation, as it pertains to daily retrieval of pathol

Assists pharmacists and administrative staff in the provision of pharmaceutical care services. Responsible for participation in pharmacy operations, medication distribution, inventory control, Omnicell usage, and maintenance of personal technical competency. Technical skills required include expertise in Omnicell use and medication preparation. Additionally, provides exem

Data entry of test orders, presort, pickup and delivery of processed specimens to the laboratory, centrifugation and aliquoting Process specimens to be sent out to additional facilities Prepare laboratory specimens for various analysis and testing Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands the

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply t

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for complex research protocols related to treatment, a

Data entry of test orders, presort, pickup and delivery of processed specimens to the laboratory, centrifugation and aliquoting Process specimens to be sent out to additional facilities Prepare laboratory specimens for various analysis and testing Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands the

Working very independently and under very general supervision from Research Manager and/or Principal Investigator, provides support to clinical research studies. May be responsible for the following activities making independent judgment of suitability of potential participants for clinical trials and registries, screening and scheduling potential participants for clinica

Collects and organizes patient data Maintains records and databases Uses software programs to generate graphs and reports Recruiting patients for clinical trials, conducts phone interviews and schedules patients for visits. Obtains patient study data from medical records, physicians, etc. Conducts library searches Performs administrative support duties as required Verifie

Level Entry Job Location IDX Needham MA Site NEEDHAM, MA Education Level High School   Job Category Biotech Description The Lab Aide I is responsible for supporting the Histology department with all clerical and ancillary duties in keeping all equipment ready to run for patient output. This position works under the direction of the supervisor and follows standard Labo

The MSL will play a pivotal role in the education of healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Limb Girdle Muscular Dystrophy as well as Sarepta's investigational therapeutics and product pipeline. Reporting to the East Region Team Leader, the MSL position will play a pivotal role in the education of healthcare professionals (HCPs) about Duchenn

We're offering a generous sign on bonus of $3,000.00 to welcome you to our team. Recognizing and valuing exceptional talent, we're eager to discuss the exciting details of this bonus during our interview process. Sign On Agreement Terms 12 month work commitment Half payment distribution after 90 days of hire and remaining 50% at one year of hire. Agreement authorizes repa

We're saving lives, building careers, and reimagining healthcare. We can't wait to grow alongside you. Job Profile Summar y This role focuses on performing work related to research and development of new products, innovation, and improvement of products and processes . In addition, this role focuses on performing the following Research Programs and Projects duties Supports

Lead the establishment, development, and lifecycle management of primary container (syringe), device, and combination product programs to support Alnylam's portfolio of products Interacts with clinical development partners (Clinical Ops, Regulatory, and Commercial) to provide expert development advice to assist the product teams Collaborate with expertise areas (Quality,

as outlined by CLIA Testing Personnel are responsible for specimen processing, test performance and for reporting test results. 1. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results; 2. Maintain records that demonstrate that proficiency testing samples are tested in the same mann