Scientific Writing Jobs in Freeport, IL

ESSENTIAL DUTIES AND RESPONSIBILITIESIn this role the Peer Writing Mentor will:Work with the Instructional Services Support Specialist and staff to ensure consistent quality service to Walden students.Correspond with students by means of an assigned weekly email shift using Outlook in More...

ESSENTIAL DUTIES AND RESPONSIBILITIESIn this role the Peer Writing Mentor will:Work with the Instructional Services Support Specialist and staff to ensure consistent quality service to Walden students.Correspond with students by means of an assigned weekly email shift using Outlook in 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 Associate Scientific/Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health care professional and provider interactions (Payers Patients Prescribers and Providers); generation of clinical and scienti More...

Description: Job Description: Medical Information Specialist (MIS) Pay :BR/Hr We are seeking a dynamic and highly skilled Medical Information Specialist (MIS) to join our team and support the Medical Science Liaison (MSL) team. This role is essential for optimizing the effectivene More...

Amick Brown is seeking an experienced Medical Information Specialist (MIS) for our direct client. Location: Remote CA Duration: 1 Year Estimated pay range: $48 60 per client contract and candidate skills experience and work location. Job Description We are seeking a d More...

Job Title Validation Process Monitoring and Data Analytics Engineer Location Parsippany NJ Hybrid Onsite T/W/Th Working hours: 84:30 8:305 95:30 type of hours (most of team works 95) Job Duration: 12 months Responsibilities: Strong background in statistics process monitori More...

Job Title: Regulatory Project Management (RPM) Location: Foster City California preferred but open to remote candidates Job Duration: 9 months POSITION OVERVIEW: With increasing independence you will support other Development team members with project and/or process administrative 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...

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...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The com More...

Description: Position Overview: We are seeking a skilled Benchling ELN Engineer to join our team. The ideal candidate will have experience in implementing and configuring Benchlings Electronic Lab Notebook (ELN) platform to support our research and development activities. The candida 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...

About this roleThe Sr Manager Medical Information Rare Disease is primarily responsible for responding to Medical Information inquiries by creating associated Standard and NonStandard materials. The position functions in an acrosstheglobe capacity (beyond that of the typical Local or More...

About This Role:Pharmacometric analyses and insight are critical in the development of drug candidates determination of product viability and maximization of commercial value at Biogen. The Associate Director Pharmacometrics has responsibility for high priority clinical development as 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...

About this roleThe Associate Medical Director Neuropsychiatry role is a part of US Medical Affairs a strategic partner within Biogen that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes.  As a key member of the US Ne More...

About This RoleThe Medical Director Nephrology (Immunology) role is a part of Specialty Care North America (US) Medical Affairs a strategic partner within Biogen that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. As a k 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...

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...