The Real World Evidence (RWE) lead provides clinical leadership for evidence generation activities, supporting the integration of RWE into Sarepta key strategic initiatives. The role functions in a company matrix team environment interacting with several key stakeholder groups including; Clinical Development, Pharmacovigilance, Regulatory Affairs, Quality Assurance, Manufa

TheCTA is responsible forsupporting the Clinical program teams and may assist the teams across multipleclinical studies. The CTA would also participate in broader clinical operationsactivitiesand initiatives such as the development and refinement of new processes. Responsibilities Clinical Study and Program Support ~70% Support clinical study teams in the delivery of key

PHARMACY ORDER ENTRY TECHNICIAN Job Locations US MA LOWELL ID 2024 138271 Line of Business PharMerica Position Type Full Time Our Company PharMerica Overview Join our PharMerica team! PharMerica is a closed door pharmacy where you can focus on fulfilling the pharmaceutical needs of our long term care and senior living clients. We offer a non retail pharmacy environment. O

Perform administrative support duties to assist the investigative team Attend individual and team meetings Conduct literature review and library searches Assist with developing and managing IRB protocols for the study Assist with recruiting patients for clinical trials Verify subject inclusion/exclusion criteria Provide basic explanation of study and obtains informed cons

of Key Responsibilities Develop, implement, and oversee Alnylam's Clinical Trial Oversight strategy in alignment with ICH GCP E6 and E8 Lead, direct, and support Clinical Trial Oversight Leads (CTOLs) in assessing CRO monitoring effectiveness across the portfolio Direct day to day work activities for FSP vendor for Clinical Trial Oversight Consistently manage oversight act

Provide expert guidance to healthcare professionals on cleaning, disinfection, and sterilization processes, including best practices, regulatory compliance, and the use of our products. Utilize scientific methods to draw fact based conclusions during testing for design verification or for troubleshooting and problem solving. Collaborate with the director CDS to ensure the

Primary Work Address 16 Divinity Avenue, Cambridge, MA, 02138 Current HHMI Employees, click here to apply via your Workday account. The Howard Hughes Medical Institute (HHMI) advances the discovery and sharing of scientific knowledge to benefit us all. As a biomedical research organization and philanthropy, HHMI supports a vibrant community of academic researchers, educato

Lead and manage integration of all project team activities, leveraging internal and development partner resources, expertise and knowledge, along with optimizing CRO resources, expertise and knowledge. Provide strategic input and execution of clinical trials from protocol design to the final clinical study report for specified studies Provide leadership and input into glo

Parexel is one of the only CROs to provide a broad depth of Clinical Pharmacology, Modeling and Simulation (CPMS) expertise to our clients, and the group is growing its capabilities and expanding globally!We currently havetremendous opportunities available to join this extremely collaborative and super friendly team! If you're looking for an opportunity to expand professi

The Clinical Research Coordinator II works closely with Health. Informatics and Implementation Science and Department of Medicine Faculty and is responsible for independently performing delegated tasks and procedures involving human subject research. Faculty conduct health policy, health equity, and digital health research with minoritized communities. This work includes

Responsible for directing quality management efforts to ensure continuous improvement and organizational excellence, adherence with all regulatory, compliance, accreditation, and legal issues, and promote a safe environment for all employees, patients and visitors. Manage risk issues and oversees the credentialing function for medical staff. Accountable for the developmen

1. Provides assistance on clinical research studies as per study guidelines and protocols. 2. Recruits and evaluates potential study patients. Per protocol instruction, conducts in person or telephone interviews or schedules patient for study visit and screening. May be required to perform clinical tests such taking vital signs, urine screens, etc. 3. Interact with patien

Parexel is one of the only CROs to provide a broad depth of Clinical Pharmacology, Modeling and Simulation expertise to our clients, and the group is currently seeking an intellectually curious and highly innovative Clinical Pharmacology / PK Director to bring their high level of motivation to our team and help our clients reduce the time to bring new treatments to patien

Position available immediately McLean Hospital is a comprehensive psychiatric hospital committed to providing easy access to superior quality, cost effective mental health services in the Boston area, Massachusetts and beyond. Since 1811, McLean Hospital has been a world leader in the treatment of mental illness and chemical dependency, research into the cause of mental i

S trategy/Business Development and Innovation Financial Management People Management Qualifications About You Customer/Patient Focus Builds strong customer/patient relationships and delivering customer/patient centric solutions Values Differences Recognizes the value that different perspectives and cultures bring to an organization Builds Effective Teams Builds cohesive t