. Actively manages and tracks study financial activity of assigned disease center in the Clinical Trials Management System (CTMS... experience required. Working knowledge of the clinical trials lifecycle preferred. KNOWLEDGE, SKILLS, AND ABILITIES...
across multiple complex disease centers and sites of service in the Clinical Trials Management System (CTMS) and works closely...-year of hire Experience and knowledge of the clinical trials lifecycle. KNOWLEDGE, SKILLS, AND ABILITIES...
, budgets and contingency/risk management plans to assure successful execution of the clinical trials in compliance with Good...Job Title: Clinical Research Director Location: Cambridge, MA About the Job Are you ready to shape the future...
all clinical trials for projects in development (excluding studies managed by TMCP) and clinical studies for marketed drugs...Job Title: Clinical Scientist Location: Cambridge, MA About the Job Are you ready to shape the future of medicine...
preferred MCA Certification within 1-year of hire No experience required Working knowledge of the clinical trials lifecycle...Responsibilities Submits study financial account creation requests for each new Clinical Research contract budget in...
clinical trials in compliance with Good Clinical Practice (GCP), applicable laws and regulations as well as applicable standard...The Clinical Research Director (CRD) is noted as the primary clinical expert for programs. The role requires...
. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials...Global Market Access & Pricing Specialist - VIE Contract Location: USA, Cambridge Target start date: 01/02/2025...
employment. Experience in both early and late-stage clinical trials. About Actalent Actalent is a global leader in...Job Title: Regulatory Submissions Specialist Job Description We are seeking a highly skilled Regulatory Submissions...
) - will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted...Overview As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation...
, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols... of experience in Medical Affairs with Global Medical Affairs experience highly preferred. Minimum of 4 years of clinical trials...
) - will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted...Overview As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation...