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

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

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

Summary Performs clinical tests for the detection and diagnosis of disease. All essential functions performed in this position reflect the age specific needs of the patients. Refers unusual situations to Sr. Medical Technologist or Manager for clarification and/or guidance in handling. Responsibilities Demonstrates understanding of Hospital s Mission Vision and Values. De

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

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

Parexel has an exciting opportunity to join our Clinical Operations Leader team. We currently have a home based Manager, Clinical Operations Leaders position that can be located in the US or Canada. The Manager, Clinical Operations Leaders is responsible for their team's performance, training and development. This includes ensuring successful performance and delivery of t

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

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

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

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

Works with Precision Medicine Strategy Lead as well as clinical study teams to ensure quality samples and data are delivered to support biomarker evaluation and delivery of science to medicine. Responsibilities include oversight of clinical sample collection, usage per informed consent form, sample tracking (chain of custody) and sample destruction. Individual will work c

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,