Clinical Study Manager - Durham, NC

+Job summary · The Clinical Study Manager provides guidance and oversight to internal and external project team members for the successful management of all aspects study operation management in accordance with GCP/ICH Guidelines, · Monitors adherence to the regulatory/essential ...

Accountable for regional study delivery with appropriate inspection readiness quality · Regional clinical operations team lead · ...

We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. · Provides guidance and oversight to internal and external project team members for the success ...

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? · ...

The Clinical Study Manager is accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget. · ...

We are seeking an experienced Clinical Data Manager to support the closeout of clinical trial studies. · Clinical study data review and support database lock activities · Design and validate clinical databases, including logic checksDevelop and execute Data Management Plans (DMPs ...

Direct and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources. · ...

Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs. · ...

The Clinical Study Manager is responsible for the day‑to‑day operational management of one or more clinical studies. · ...

The Clinical Study Manager is responsible for the day‑to‑day operational management of one or more clinical studies. · ...

The Oncology Clinical Research Unit (CRU) at the Duke Cancer Institute (DCI) is seeking a Senior Clinical Research Coordinator to join our Thoracic, Sarcoma, Head & Neck, and Genitourinary (GU) Clinical Research Program. In this role you will lead a dynamic team coordinating mult ...

We have a functional service provider solution which is a unique partnership that allows our customers to leverage the experience of our staff while allowing you to gain direct experience working onsite at a pharmaceutical/biopharmaceutical company. · Accountable for achieving th ...

The Oncology Clinical Research Unit (CRU) at the Duke Cancer Institute (DCI) is seeking a Senior Clinical Research Coordinator (CRC Sr.) to join our Thoracic, Sarcoma, Head & Neck, and Genitourinary (GU) Clinical Research Program.Lead the coordination and implementation of multip ...

· This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Country Study Operations Manager - REMOTE. In this role, you will be pivotal in overseeing clinical studies from inception to completion, ensuring that they adhere to tim ...

We are looking for an experienced ISR/CO Study Manager to support our large portfolio of Investigator Sponsored Research (ISR) and collaborative (CO) studies. · Manage global ISR and collaborative studies ensuring compliance scientific integrity timely progression. · Serve as ope ...

We are looking for an experienced Project Manager II to support our late-phase oncology research studies. As a key member of our team, you will partner closely with Medical Affairs and principal investigators to drive studies to completion and support their path to publication. · ...

Job summary:Provide technical and administrative support to the Clinical Operations team by coordinating and conducting various responsibilities of clinical studies.Maintains the company's Clinical Trial Management System (CTMS) and Project Study File (PSF) in accordance with Goo ...

To perform experiments ensuring that projects are completed to plan while complying with all quality and safety regulations. · Assist with study plan writing data analysis and interpretation and report writing. · ...

This full-time onsite Clinical Research Professional will support research led by Principal Investigators in the Division of Nephrology. · ...

The Clinical Research Associate assists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, · IHC/GCP Guidelines, company SOPs, and study protocols. · We are leaders in plasma-derived medicines and transfusion medic ...