Clinical Trial Documentation Specialist

Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant to our direct client, a global medical device company in Fort Worth, TX (hybrid work schedule).Job Title: Technical Documentation Specialist II (Contractor)Pay Range: $37.86/hr - $41.43/hr (W-2)The contract duration is initially 2...

Job OverviewTalentBurst is seeking a skilled Documentation Specialist II to coordinate clinical trial documentation for a 24-month project in Fort Worth, TX.

Job Title: Regulatory Documentation Coordinator - Clinical TrialsJob OverviewSource One Technical Solutions, a WBENC certified woman-owned company, provides a full range of professionals to various industries nationwide. We are currently seeking a Regulatory Documentation Coordinator - Clinical Trials for our client in Fort Worth, TX.Key...

Are you passionate about driving innovation in clinical research? We're seeking a detail-oriented and proactive professional to play a key role in supporting the success of clinical trials. As a Clinical (Technical) Documentation Specialist, you'll ensure the seamless coordination, accuracy, and organization of critical trial documents while collaborating...

Title: Technical Documentation Specialist Location: Fort Worth, TX Duration: 24 months+ Job Description: Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions. Ensure accuracy and quality of site documents included in the site initiation packets and...

Job DescriptionAt Aequor Information Technologies Pvt. Ltd., we are seeking a highly organized and detail-oriented Clinical Trials Coordinator to join our team.We offer an attractive compensation package of $65,000 per year for this role.Key Responsibilities:Coordinate the collection and processing of trial documents between investigator sites and our...

Technical Documentation Specialist II Clinical Fort Worth, TX, US Pay Rate Low: 30.00 | Pay Rate High: 42.00 Added - 25/11/2024 Apply for Job Exciting Doumentation Specialist development opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world – with complementary businesses in Surgical...

Job title: Technical Documentation Specialist II Job ID: 24-05255 Location: Fort Worth, TX (Onsite) Duration: 24 months on W2 Contract Interviews:1, possibly 2. Job Description: Coordinate collection and processes essential trial documents between investigator sites and Client CRD, including preparation and/or facilitating IRB/IEC...

Job Description: • Coordinate collection and processes essential trial documents between investigator sites and Alcon CRD, including preparation and/or facilitating IRB/IEC submissions. • Ensure accuracy and quality of site documents included in the site initiation packets and throughout the duration of the study. • Enter and maintain site information...

Are you passionate about driving innovation in clinical research? We're seeking a detail-oriented and proactive professional to play a key role in supporting the success of clinical trials. As a Clinical (Technical) Documentation Specialist, you'll ensure the seamless coordination, accuracy, and organization of critical trial documents while collaborating...

Job Title: Technical Documentation Specialist II Location: Ft Worth, TX Duration: 24 Months Job Description: Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions. Ensure accuracy and quality of site documents included in the site initiation...

Astrix Technology is a global leader dedicated to helping people see brilliantly.We have an exciting opportunity for a Technical Documentation Specialist II to join our team!Job Summary:This role is responsible for coordinating the collection and processing of essential trial documents between investigator sites and CRD, including preparation and/or...

Benefits: Coordinate collection and processes essential trial documents between investigator sites and Alcon CRD, including preparation and/or facilitating IRB/IEC submissions. • Ensure accuracy and quality of site documents included in the site initiation packets and throughout the duration of the study. • Enter and maintain site information and...

**Overview**Texas Oncology, Inc. is a leading provider of community-based cancer care in the United States. We are seeking an experienced Clinical Research Nurse (RN) to join our team at our Ft Worth location.This full-time position offers a competitive salary of $95,000 per year and a comprehensive benefits package. As a member of our clinical research...

A global company, we work in over 70 countries and serve patients in more than 140 countries. We have a long history of industry firsts, and each year we commit a substantial amount in Research and Development to meet customer needs and patient demands. Our leadership is grounded in cutting-edge innovation and breakthrough technology, transforming the way we...

Job Title: Technical Documentation Specialist II Location: Ft Worth, TX Duration: 24 Months Job Description: Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions. Ensure accuracy and quality of site documents included in the site initiation packets...

Job Title: Technical Documentation Specialist II Location: Ft Worth, TX Duration: 24 Months Job Description: Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions. Ensure accuracy and quality of site documents included in the site initiation...

Job Title: Technical Documentation Specialist II Location: Ft Worth, TX Duration: 24 Months Job Description: Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions. Ensure accuracy and quality of site documents included in the site initiation...

Job OverviewWe are seeking a highly skilled Medical Device Documentation Expert to join our team at Source One Technical Solutions. This is a unique opportunity to work as a consultant with a global medical device company in Fort Worth, TX.Key Responsibilities:Coordinate the collection and processing of essential trial documents between investigator sites...

Job Title: Technical Documentation Specialist II Location: Ft Worth, TX Duration: 24 Months Job Description: Coordinate collection and processes essential trial documents between investigator sites and *** CRD, including preparation and/or facilitating IRB/IEC submissions. " Ensure accuracy and quality of site documents included in the site...