Trial Preparations Jobs in Newton, MA

This role is parttime (2030 hours/week) hybrid (average 1 day/week in the Newton MA office) and temporary (6 month contract) with the possibility for conversion to a fulltime permanent role. Research Professional 1 Job Posting ID SIMNJP Period 04/01/2025 to 09/30/ More...

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...

Job Description:Provides escrow services for residential and commercial resale new construction refinance relocation and timeshare transactions. Responsible for supporting real estate transactions by providing a range of administrative and/or support duties to assist escrow processes 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...

About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri 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...

Description: Join our team now at Client as a Clinical Trial Assistant. This role is parttime (2030 hours/week) hybrid (average 1 day/week in the Newton MA office) and temporary (6 month contract) with the possibility for conversion to a fulltime permanent role. This is a role well 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...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide The below client is with one of our client which is a leading global medical technology company. It offers a wide ran 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...

Job Title: Clinical Data Associate Duration: 06 months contract with possible extension Shift Details: Day shift/ Fully Remote Pay Range: $30$37 /hr w2 Essential Duties and Responsibilities: Works collaboratively with Process Engineers and Statisticians in Global Manufact More...

Description: Works collaboratively with Process Engineers and Statisticians in Global Manufacturing Sciences and Technology (GMSAT) Statistical Sciences & Analytics (SS&A) team to meet project deliverables and timelines to author and approve Continued Process Verification (CPV) relat 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...

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...

Description: 100% onsite Oceanside CA Hours: MonFri business hours Reason for opening: continued/extra workload (projects) Role: Senior Research Associate Biologics Drug Product Development (BDPD). Duration: 12 months could possibly extend additional time however that wont be know 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...

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...