Trial Preparations Jobs in Indianapolis, IN
Trial Preparations Jobs in Indianapolis, IN
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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...
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...
Position Overview:This position will provide strategic tactical and operational direction and support to expedite development of our clients clinical trial portfolio by helping to develop successful regulatory strategies and submissions in support of clinical trials. This positio More...
Position Overview:This position will provide strategic tactical and operational direction and support to expedite development of our clients clinical trial portfolio by helping to develop successful regulatory strategies and submissions in support of clinical trials. This positio 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: 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...
Job Title: Research Associate III Location: Oceanside CA Duration: 12 months with possible extension Shift Details: 9am5pm Pay Range: $40$47/hr w2 Essential Duties and Responsibilities: Protein formulation/stability of various dosage forms (liquid/lyophilized) and configurations 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...
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...
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...
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...
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