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Idaho State Job Bank Boise, United StatesSenior Manager, Training Development and Delivery at Takeda Pharmaceuticals in Boise, Idaho, United States Job Description By clicking the 'Apply' button, I understand that my employment application process with Takeda will commence and that the information I provide in my applic ...
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Cardiology Clinical Research Coordinator Full
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Idaho State Job Bank Boise, United StatesSenior Clinical Research Monitor, Western Region at Edwards Lifesciences in Boise, Idaho, United States Job Description Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our inn ...
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Idaho State Job Bank Boise, United StatesSenior Country Clinical Quality Management Lead (Remote) at Merck in Boise, Idaho, United States Job Description Job Description It is critical that, for all company-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and regulati ...
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Trinity Health Corporation Boise, ID, United StatesEmployment Type: · Part time · Shift: · Description: · Location: Saint Alphonsus Regional Medical Center · Status: PRN · Call: No Call · Salary and Benefits: · * Market-based salary · * Malpractice Insurance (Incl. Tail) · Practice Highlights: Saint Alphonsus Medical Group (SAMG) ...
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Trinity Health Boise, ID , USA, United States**Employment Type:** · Part time · **Shift:** · **Description:** · **Location:** **Saint Alphonsus Regional Medical Center** · **Status** : PRN · **Call** : No Call · **Salary and Benefits** : · + Market-based salary · + Malpractice Insurance (Incl. Tail) · **Practice Highlights: ...
Senior Clinical Trial Coordinator - Boise, United States - Idaho State Job Bank
Description
Senior Clinical Trial Coordinator at J&J Family of Companies in Boise, Idaho, United States Job Description Senior Clinical Trial Coordinator W Description Abiomed, part of Johnson & Johnson's MedTech is recruiting for a Senior Clinical Trial Coordinator II, located in Danvers, MA or Remote.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at The Senior Clinical Trial Coordinator (Sr. CTC) supports the planning and coordination in all aspects of clinical trial operations.This position requires a thorough understanding of clinical trials, including how to support a trial from site feasibility/qualification to site activation.
A Sr.CTC will work closely with the clinical project team to collect all essential regulatory documents for a clinical study (at both study and site level) in a timely fashion and store appropriately while ensuring compliance with ICH/GCP guidelines, federal regulations, and corporate policies and procedures.
The position involves interaction with internal and external customers and partners, and must operate with a high degree of discretion, as the role involves handling information of a confidential and critical nature.
Key Responsibilities:
+ Take a lead role in management of trial-related systems such as the electronic Trial Master File (eTMF), including set up, maintenance and study close out. + Assures collection of essential clinical trial documents (i.e., CVs, Medical Licenses, Laboratory documentation, Financial Disclosures, Investigator Agreements) from investigational sites for efficient study start-up/site activation. + Support site start-up activities including reviewing study specific ICF templates, managing and communicating the status of sites and study's start-up progress. + Plan, coordinate, and arrange study communications on and off-site with both internal and external partners. + Responsible for supporting the drafting of meeting agendas and detailed meeting minutes. + Maintain quality of collected regulatory documents, which To view full details and how to apply, please login or create a Job Seeker account