Trial Records Jobs in Whiteville, TN

Acts as a specialized liaison to assist sites with a protocoltailored approach to increase efficiency of the patient identification and recruitment processAssists sites in developing and implementing patient enrollment techniquesCoordinates site specific patient recruitment and retent More...

Description: The ideal candidate will have thorough knowledge of Clinical investigation of medical devices for human subjects Good Clinical Practice (ISO 14155) 21 CFR partand other applicable regulations. Roles & Responsibilities: Contribute to all clinical research activitie More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...

*Can be remote in the US or EUProvides specialist medical and scientific strategic and operational input into core medical affairs activities such as: healthcare professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value More...

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II More...

What is it for you: Experienced Trial Attorneys certified by the New Jersey Supreme Court in civil criminal and workers compensation matters Six New Jersey offices and additional locations in New York City and suburban Atlanta offer comprehensive regional coverag outstanding bene More...

Take your career to the next level and be involved in study startup processes in the US. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. HomebasedYou will:Supports all processes critical for site activ More...

About This RoleAs a Senior Manager Aggregate Report Scientist you will be an integral part of the Safety Surveillance and Aggregate (SSA) Reports team. In this pivotal role you will oversee the pharmacovigilance processes for all aggregate reports including PSURs DSURs PADERs and loca More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards More...

Reporting to the Global Marketing Director Demand Generation who is based in Melbourne Australia the Sr. Marketing Manager AMER will play a critical role in shaping and executing Ignitions local marketing strategy for the US. This is a handson highly collaborative role that involves p More...

The Director of Network Strategy is responsible for leading the strategic planning and optimization of Milestone Ones partnership with clinical research sites. The position requires a strong analytical mindset crossfunctional collaboration and strong leadership skills. This role will More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

JOB TITLE: Vendor Qualification Associate I Onsite: Foster City Hybrid: 3 days a week minimum Description Client is looking for a Vendor Qualification Associate I who will report to the Senior Manager of Vendor Outsourcing. The candidate will be responsible for ensuring high quality More...

destinationone Consulting specializes in recruitment across diverse sectors including CleanTech Education and EdTech Government (Municipal State/Provincial and Federal) Health and MedTech Healthcare and Wellness Legal NotForProfit and Public Accounting. We are committed to building a More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

Drives key innovative and strategic projects and priorities for USMA oncology. Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions; generation of clinical and scientific data More...

The Senior Associate Counsel Clinical Trials and Research provides legal support for clinical trial and research activities across the University of Maryland Medical System (UMMS). This role involves refining processes to streamline timetoactivation for clinical trials standardizing c More...

About This RoleThis role reports into the Head of Aggregate Reports and will be part of the Safety Surveillance and Aggregate Reports (SSA) team. The Associate Director Pharmacovigilance Scientist is responsible for managing the processes for all Aggregate Reports such as PSURs DSURs More...