Senior Research Specialist Job at University of Rochester (Rochester)

Senior Research Specialist

The Senior Research Specialist provides direct research support at the senior pr...

Location

United States of America , Rochester

Salary:

63815.00 - 95723.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree required
Master's degree preferred
5 years of related experience
or an equivalent
or a combination of education and experience required
Applicants should be self-motivated and capable of working independently as well as in a collaborative setting required
Strong interpersonal and communication skills, including written communication required
Ability to readily learn new experimental techniques required
Strong analytical, communication, organizational and computer skills required

Job Responsibility

Collaborates with investigators in writing protocols for the conduct of research
Organizes research activities in accordance with approved protocols
Informs staff of their responsibilities in the project
Develops and installs operating procedures for the laboratory
Ensures that health and safety practices are maintained
Analyzes and evaluates experimental data and interprets results
Prepares written reports and presentations on all on-going projects
Keeps abreast of trends in field of interest
Independently operates histological-related equipment and microscopes
Maintains contact with outside research laboratories, vendors and technical representatives

Fulltime

Experience Research Senior Specialist

The Experience Research Senior Specialist is a key member of the team who suppor...

Location

Canada , Toronto

Salary:

83000.00 - 132000.00 CAD / Year

Mastercard

Expiration Date

Until further notice

Requirements

4 years’+ experience in user experience research, market research, behavioral research, or related fields within innovation-driven organizations
Proven experience in a broad range of qualitative and quantitative research methods including ethnography, contextual inquiry, usability testing, surveys, analytics interpretation, and experimental design
Experience in synthesizing complex data sets and translating research findings into clear, actionable insights that influence product and business strategy
Familiarity with product development lifecycles, MVP concept testing, and iterative design processes
Storytelling and communication skills, with experience presenting research findings to diverse audiences

Job Responsibility

Support the lead researcher or strategist in identifying and prioritizing the riskiest assumptions to subsequently de-risk
Support in choosing the optimal research approach and methodology to de-risk priority assumptions, taking into consideration business needs and project phase
Aid in the design and conducting of rigorous, mixed-methods research studies to uncover customer needs, motivations, behaviours, and pain points, across all phases of the product development lifecycle -- from framing the problem to testing and iterating concepts
Help the lead researcher or strategist in defining research plans, goals and objectives, and develop recruitment screeners, discussion guides and surveys focused on testing assumptions, and informing actionable product and business decisions
Support in the partnering with third-party vendors to execute and scale research plans as needed
Aid in the synthesis of qualitative and quantitative data into clear insights, opportunity areas, and actionable recommendations that inform product and business strategy
Support the communication of research findings through compelling storytelling, presentations, and reports to senior stakeholders
Collaborate closely with other researchers and strategists to translate insights into strategic frameworks, value propositions, and MVP hypotheses
Support the planning and facilitation of cross-functional design thinking workshops
Collaborate with the CX team to support the design of optimal testing stimuli based on research needs

Fulltime

Senior Clinical Research Specialist

The Senior Clinical Research Specialist will conduct clinical research throughou...

Location

United States , Burnsville

Salary:

105000.00 - 147000.00 USD / Year

Imricor Medical Systems

Expiration Date

Until further notice

Requirements

BA/BS education in relevant discipline required
5 years clinical experience in the medical device industry strongly preferred
Highly skilled and proficient at clinical trial management/execution
Conduct complex work under minimal supervision and with wide latitude for independent judgment
Experience with Microsoft Office: Word, Excel, PowerPoint

Job Responsibility

Prepares and authors clinical documents such as: protocols, patient informed consents, case report forms, clinical trial agreements, and/or investigator brochures/report of prior investigations as needed
Develops and executes site training on protocol and data management requirements
Communicates with Regulatory agencies (FDA, European Competent Authorities, etc) to develop and implement clinical trials to support our products
Develops monitoring plans and monitors or oversees monitoring of clinical sites
Oversees adverse event review committees and/or data review committees as necessary (develop and execute charters)
Identifies and communicates with CROs as necessary based on study needs
Oversee and resolve operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations
Prepares and maintains clinical trial budgets for specific projects
Authors clinical reports (interim and final) for both regulatory bodies and publications as necessary
Communicates cross functionally with multiple stakeholders in the company – including regulatory, marketing, product development

What we offer

Medical
Dental
Vision
Health Savings Accounts
Health Care & Dependent Care Flexible Spending Accounts
Disability Benefits
Life Insurance
Retirement Benefits

Fulltime

Senior Clinical Research Specialist

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

60431.00 - 84603.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 3 years of relevant experience required
Ability to effectively manage complex research protocols/procedures required
Fully adheres to applicable safety and/or infection control standards
Proficiency in medical terminology, the clinical research process, and applicable regulatory guidelines, standards preferred
Proficiency in managing multiple and competing priorities/demands
Thorough knowledge of and established track record in assuring GCP, Responsible Conduct of Research standards, applicable safety standards, and OSHA guidelines throughout study implementation
Exceptional interpersonal, organizational, and time management skills
highly collaborative, promotes teamwork
Ability to build collaboration among research team members, laboratory staff, patients, and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients)
Proficient in MS Office (e.g., Word, Excel, and PowerPoint), email, and internet

Job Responsibility

Provides leadership in planning, implementing, monitoring, and evaluating multiple clinical research protocols
Manages the day-to-day operations of multiple studies, carrying out study coordination duties from protocol development and initiation through to study close-out in accordance with regulatory/sponsor guidelines
Monitors and maximizes adherence to research standards, regulatory guidelines, and approved operational procedures
Works closely with study team members and other study sites to ensure the safety and adherence of study participants to the study protocol
Manages study-related administrative and human resources tasks and facilitates across-the-board flow of information, orchestrating study activities and personnel
Coordinates enrollment of participants
Oversees and facilitates eligibility screening and study recruitment activities
Plans study timelines and schedules appointments and study visits
Manages and organizes case report forms, source documents, and research records
Enters research data into data collection forms and/or study databases

Fulltime

Environmental Research Safety Specialist, Senior

Manage and oversee portions of the Accreditation Environment of Care (TJC), and/...

Location

United States , Charlotte; Winston Salem

Salary:

44.15 - 66.25 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Bachelor’s Degree Environmental Health and Safety
Minimum 5 years of experience in related discipline required (safety and/or facilities management that includes experience in emergency management, environmental safety, and life safety)
Must have the ability to clearly communicate verbally, in person, and in writing with patients, families/agencies and the health care team
Must possess a sense of urgency and make sound decisions
Responsible for setting a strong example of safety by working safely and utilizing personal protective equipment (PPE) appropriately
Critical thinking and independent decision making and is solution oriented
Ability to operate computer and computer software programs
This position requires travel, therefore, will be exposed to weather and road conditions
Travel to other facilities in a personal vehicle is required
Must be able to sit, stand, walk, lift, squat, bend, reach above shoulders, and twist frequently throughout the workday

Job Responsibility

Manage and oversee portions of the Accreditation Environment of Care (TJC), and/or Physical Environment (DNV) Safety programs for multiple Advocate facilities
Act as liaison for all chapters (Safety, Security, Hazardous Materials/Waste, Clinical Engineering, Fire Safety and Utilities) within the program
Coordinate and chair the Environment of Care or Physical Environment Committee, maintain committee agendas and minutes, communicate safety updates to committee
Assists with, Occupational Health and Safety (OSHA), Environmental Compliance (EPA), Construction Safety, and Operations activities to maintain constant readiness for surveys and inspections
serves as a safety point of contact during federal, state, local and organizational surveys, and inspections
Supports regulatory agency personnel during compliance inspections
Interfaces with Advocate Facility Administration and Department Leadership to oversee special projects as directed by Safety Leadership and Facility Administration
Presents safety programs, safety updates, and/or training to leadership, physicians, vendors/contractors, and teammates
Discuss safety and risk assessment impacts to operational changes that has effect on patient safety, teammate safety, visitor safety, and life safety
Initiate and disseminate PCRA (Pre-Construction Risk Assessment), ICRA (Infection Control Risk Assessment) and ILSM (Interim Life Safety Measures) documentation for projects at multiple facilities

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance

Fulltime

Environmental Research Safety Specialist, Senior

Manage and oversee portions of the Accreditation Environment of Care (TJC), and/...

Location

United States , Charlotte; Winston Salem

Salary:

44.15 - 66.25 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Bachelor’s Degree Environmental Health and Safety
Minimum 5 years of experience in related discipline required (safety and/or facilities management that includes experience in emergency management, environmental safety, and life safety)
Must have the ability to clearly communicate verbally, in person, and in writing with patients, families/agencies and the health care team
Must possess a sense of urgency and make sound decisions
Responsible for setting a strong example of safety by working safely and utilizing personal protective equipment (PPE) appropriately
Critical thinking and independent decision making and is solution oriented
Ability to operate computer and computer software programs
This position requires travel, therefore, will be exposed to weather and road conditions
Travel to other facilities in a personal vehicle is required
Must be able to sit, stand, walk, lift, squat, bend, reach above shoulders, and twist frequently throughout the workday

Job Responsibility

Manage and oversee portions of the Accreditation Environment of Care (TJC), and/or Physical Environment (DNV) Safety programs for multiple Advocate facilities
Act as liaison for all chapters (Safety, Security, Hazardous Materials/Waste, Clinical Engineering, Fire Safety and Utilities) within the program
Coordinate and chair the Environment of Care or Physical Environment Committee, maintain committee agendas and minutes, communicate safety updates to committee
Assists with, Occupational Health and Safety (OSHA), Environmental Compliance (EPA), Construction Safety, and Operations activities to maintain constant readiness for surveys and inspections
serves as a safety point of contact during federal, state, local and organizational surveys, and inspections
Supports regulatory agency personnel during compliance inspections
Interfaces with Advocate Facility Administration and Department Leadership to oversee special projects as directed by Safety Leadership and Facility Administration
Presents safety programs, safety updates, and/or training to leadership, physicians, vendors/contractors, and teammates
Discuss safety and risk assessment impacts to operational changes that has effect on patient safety, teammate safety, visitor safety, and life safety
Initiate and disseminate PCRA (Pre-Construction Risk Assessment), ICRA (Infection Control Risk Assessment) and ILSM (Interim Life Safety Measures) documentation for projects at multiple facilities

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program

Fulltime

Senior Contract Specialist, Clinical Research Agreement

The Clinical Research Agreements team manages the contract negotiation of indust...

Location

United States , Boston

Salary:

69888.00 - 111831.20 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor's degree
2+ years of relevant experience
ability to effectively negotiate with peer level department heads and/or with external agencies/facilities on issues and programs that impact department as well as several other large departments/divisions

Job Responsibility

Drafts and negotiates written clinical research related agreements with corporate sponsors and other outside entities
Conducts negotiation of complex clinical research agreements and attends to relevant terms
Assures timely completion of negotiation proceedings
Acquires and maintains knowledge of Hospital’s policies and procedures applicable to clinical sponsored research
Develops functional understanding of the business needs of the hospital administrative and research staff
Evaluates and makes recommendations for systems, policies and procedures
Advises faculty on BCH and sponsor requirements for clinical corporate sponsored research agreements
Responsible for overseeing pre award administration of clinical research agreements
Supports strategies for marketing the hospital’s research capabilities and clinical trial resources to industry
Advises on quality improvement efforts

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

CI Specialist - Research Analyst Support - Senior

As an experienced CI Specialists, you will support the mission to identify, moni...

Location

United States , Fort Meade

Salary:

140000.00 - 145000.00 USD / Year

Amentum

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a relevant field and 14 years’ relevant intelligence analysis experience
with a portion of the experience within the last 2 years
High school diploma and 20 years of relevant experience
Associate degree and 16 years of relevant experience
Master’s degree and 12 years of relevant experience
Must have experience with all the following: AR 381-12 (Threat Awareness and Reporting Program)
AR 381-20 (US Army Counterintelligence)
AR 381-10 (US Intelligence)
and DoDI 5240.23 (CI Activities in Cyberspace)
Must be a graduate of in-residence Fundamentals of Intelligence Analysis course or Military Service equivalent

Job Responsibility

Conduct, develop, produce, and present programs of instruction in specified collection operations TTPs, and related or supporting processes, relevant to the various human intelligence and technical intelligence operations under DoD authorities
Provide research and analysis of existing and emerging threats and vulnerabilities to the Army Commanders and their Staff
Provide recommendations regarding the management, coordination, and training executed by the Detachment
Analyze and develop recommendations regarding the Operations Calendar to ensure requirements levied are executable against current tasks to ensure there are no conflicts, and training requirements are synchronized with operations
Conduct analysis and provide reports on personnel operations tempo to Government Team/Branch/Division Chiefs
Provide an analysis of finalized products, including Damage Assessments, Threat Assessments, and OPSEC Assessments to supported organizations
Monitor and disseminate all operations orders received from higher headquarters and ensure completion of all required administrative tasks and Army mandatory training
Conduct analysis and provide recommendations to the commander on the training readiness of the unit
Analyze and compare unit compliance with AR 350-1 training requirements, and additional requirements levied by the higher headquarters and the unit commander
Provide analysis of trends within the Battalion for use in future planning and efficiency improvement

What we offer

Health, dental, and vision insurance
Paid time off and holidays
Retirement benefits (including 401(k) matching)
Educational reimbursement
Parental leave
Employee stock purchase plan
Tax-saving options
Disability and life insurance
Pet insurance

Fulltime

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