654 Software Developer Research jobs in Franklin,MA

Bachelor's Degree in one of the following disciplines: Electrical, Mechanical, Chemical, Industrial Engineering or a science-based equivalent degree
5+ years of manufacturing process experience
5+ years of related quality assurance and quality auditing experience
Valid driver's license required
Experienced in manufacturing, quality control, and audit practices
Comfortable working independently and managing your own schedule
Tenured audit experience with demonstrated proficiency performing conformity assessment audits
Ability to obtain and assess objective evidence throughout the audit process while acting impartially and maintaining confidentiality
Observe, document, and evaluate audit observations while effectively managing customer interactions throughout the audit process
Computer literacy with demonstrated proficiency in Microsoft Office Suite
Experience with various measurement tools such as pressure gauges, calipers, voltmeters, etc.
Ability to read and interpret engineering technical drawings

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Forward Deployed Software Engineer

Growth Signals

Boston, MA 02115

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Claims Complex Property Adjuster

ACSC Management Services

Lincoln, RI 02865

$38.64-$51.46/hr

~ 29 min OnsiteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

7-9 years Prior claims handling experience. Required
7-9 years Property claims administration experience. Preferred
Advanced knowledge of insurance, coverage investigation, scope and damage assessment, negligence and subrogation principles required.
Advanced knowledge of Microsoft Office suite, general computer software and claims software.
Comprehensive understanding of building and vehicle repair procedures and third-party liability issues.
Advanced leadership skills among peers required.
Advanced organization and planning recognition skills required
Advanced oral and written communication skills required.
Advanced interpersonal skills required.
Valid Driver's License, acceptable Department of Motor Vehicles record and minimum liability insurance - Issued by State Required
An insurance/claims adjuster license may be required for claims administration in specific states.
Bachelors Equivalent combination of education and experience Preferred

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Director, Clinical Outcomes Assessment, Global Evidence & Outcomes

Takeda Pharmaceutical

Boston, MA 02108

RemoteEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Combination of academic training and practical experience (oncology experience preferred) in outcomes research is required.
Doctoral degree (e.g., Ph.D., Sc.D. or Dr.P.H.) in a relevant discipline such as, but not limited to, health services research, health outcomes research, epidemiology, pharmacy administration, public health, economics, statistics or decision sciences, plus 8+ years practical experience
Practical experience (number of years as noted above) in performing outcomes research, in any setting, including life sciences company, research organization, academic institution or governmental agency, is required.
A minimum of 5 years of Patient Reported Outcomes experience is required.
Demonstrated experience in interpreting statistical analysis is required.
Ability to communicate scientific evidence, with strong written and verbal presentation skills, is required.
Working knowledge of Patient Focused Drug Development (PFDD) Guidance documents and other relevant guidance documents and best practices is required.
Ability to understand regulatory and HTA/payer challenges for Takeda products; and to critically review data and assimilate strategies that take such environments into consideration is required.
Familiarity with the role and importance of outcomes research in the multi-disciplinary drug development and commercialization environment and process (involving multiple stakeholders) is required.
Experience should include the conduct of outcomes research studies, and the communication of study findings to internal and external audiences.
Expertise and experience with the development, psychometric evaluation and selection of PRO instruments used in clinical studies is expected.
Must be capable of leading teams, influencing teams, and driving decisions; must also be able to work effectively as a member of different teams.
Experience with the drug development process in the pharmaceutical industry is strongly preferred. Regulatory understanding and experience in negotiating PRO label claims is strongly preferred. Experience with ePRO is strongly preferred.
Oncology experience is highly desirable
Ability to work collaboratively and effectively in a multicultural and cross functional team environment.
Experience managing budgets is expected.
Demonstrated expertise in patient-reported outcomes/health-related quality of life assessment is highly desirable.
Experience in conducting outcomes research in different geographic regions and interacting with regulator and/or HTA/payer policy-makers is highly desirable.