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ALLIANCE CLINICAL LLC
Lewisville
Job Description Job Description ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. 1) Comply with all company policies, procedures, and conduct. 2) Strictly adhere to confidentiality and compliance standards. 3) Create, Maintain, Evaluate & Implement QA Plan/Policies for conducted studies. 4) Review and audi
Job Source: ALLIANCE CLINICAL LLCUL, LLC
Dallas
The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and interprets science-based reports, data and regulations in order to prepare documents for government agencies, curate lists and/or develop Environment, Health, Safety, and Transportation (EHS&T) information for the control and use of chemicals in the mark
Job Source: UL, LLCRandstad US
Fort Worth
regulatory affairs specialist ii. + fort worth , texas (remote) + posted june 10, 2024 **job details** summary + $50 - $53.57 per hour + contract + high school + category life, physical, and social science occupations + reference48290 job details job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you
Job Source: Randstad USBaylor Scott & White Health
Dallas
**JOB SUMMARY** Regulatory Affairs Specialist provides regulatory guidance, monitoring and administrative help to the Institutional Review Board, Institutional Animal Care and Use Committee and Data and Safety Monitoring Board and other people involved in the conduct of research at all Baylor Scott & White Health **ESSENTIAL FUNCTIONS OF THE ROLE**
Job Source: Baylor Scott & White HealthTCWGlobal
Fort Worth
Job Description Job Description Regulatory Affairs Specialist (R&D/QA) Fort Worth, TX 76104 (*Local candidates- 3 days on site/2 days remote) $43-$45hr (Weekly pay + Benefits) 1yr contract (Excellent potential for extension or permanent) Full-time- M-F 8am-5pm Our client is a global team of innovators, leaders, creators, builders, and problem s
Job Source: TCWGlobalClarendale of Schereville
Bedford, TX, United States
Job Description When you work at LCS Dallas Operations, you have a front-row seat to the amazing life stories of the wisest people on earth. What's more, you are part of an extraordinary company - one that's investing in the future of senior living by investing in you. Don't just do a job. Be part of an extraordinary life! LCS Dallas Operations i
Job Source: Clarendale of ScherevilleJacobs Management Group
Dallas
Job Description Job Description Clinical Specialist / Medical Device Account Specialist Join an innovative team at the forefront of revolutionizing breast cancer surgery! As a Clinical Specialist, you'll play a crucial role in the first commercialization phase of groundbreaking medical devices. This is a unique opportunity to shape the future
Job Source: Jacobs Management GroupCHILDREN'S ADVOCACY CENTER FOR NORTH TEXAS
Lewisville, TX, United States
CHILDREN'S ADVOCACY CENTER FOR NORTH TEXAS is an EEO employer - M/F/Vets/Disabled This full-time position provides client outreach and scheduling of therapeutic services with families that are involved in investigations of severe child abuse. Compensation: $42,000. Salary is based on experience. The Clinical Intake Specialist's responsibilities
Job Source: CHILDREN'S ADVOCACY CENTER FOR NORTH TEXASGrapevine, TX, United States
Iterative Health is pioneering the use of artificial intelligence-based precision medicine in gastroenterology, with the aim of helping to optimize clinical trials investigating the treatment of IBD. We use advanced machine learning and computer vision to interpret endoscopic videos along with other types of data, helping clinicians better assess patients with potential GI problems. Ultimately, the company aims to establish more meaningful endpoints to serve as better predictors of both therapeutic response and disease outcomes.
Iterative Health is seeking a Senior Clinical Regulatory Specialist to join our team. The Senior Clinical Regulatory Specialist will work under the direction of the Director of Regulatory Affairs with the primary responsibility of assisting with the conduct and compliance of Phase 2-4 pharma sponsored research studies. This position will be a collaborative individual contributor, working with internal stakeholders, clinical sites, and study sponsors–requiring Administrative and Regulatory work. This is an exciting time in the Clinical Research industry! Our team is driving the advancement of research by implementing streamlined processes, with a mission of getting treatment options to patients in a faster, more efficient way.
What you’ll be doing:
Working with clinical site staff on essential document preparation, organization, data entry and Regulatory compliance maintenance
Facilitating successful study start-up, including clinical site and sponsor communication and status reporting
IRB submissions on behalf of sites
Participating in internal and external audits
What we’re looking for:
Expertise in clinical research, regulatory & compliance and Phase 2-4 sponsored clinical research, with a deep understanding of the site Study Coordinator role
Previous experience as a clinical research coordinator is valuable
Skilled at adhering to Good Clinical Practices (GCP), FDA essential documents guidelines, and Standard Operating Procedures (SOPs)
Experience with project management and/or functional team leadership, with strong organizational, decision-making, time management, multi-tasking and prioritization skills
Expertise in Adobe, Microsoft Office (Word, Excel, PowerPoint, Outlook, Teams), and clinical trial management system (CTMS)
Confidence and experience presenting to various internal and external stakeholders
Some of our benefits include:
Vision/Dental/ Medical Insurance
Life/Disability Insurance
Parental Leave
Stock Options
Flexible Work Hours
Unlimited Paid Time Off
At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].
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Email Alert for Senior Clinical Regulatory Specialist jobs in Grapevine, TX, United States
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