Research Assistant I- Neurology Job at Boston Children's Hospital (Boston)

Clinical Research Assistant

The clinical research assistant will be an integral member of Dr. Eseosa Ighodar...

Location

United States , Winston Salem; North Wilkesboro

Salary:

30.70 - 46.05 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Master's degree with four years' experience in a research setting
or, an equivalent combination of education and experience
Clinical experience preferred
Understanding of scientific research methodologies
Ability to prepare grant proposals independently
Experience with peer-reviewed publications and poster/oral presentations
Proficiency in Microsoft Word, Excel, PowerPoint, and basic statistical analyses
Ability to manage and analyze data accurately
Strong written and verbal communication
Detail-oriented, resourceful, and able to meet deadlines consistently

Job Responsibility

Assist in developing research methodologies and protocols
Create and revise study materials
Conduct participant recruitment, screening, and interviewing, and follow-up activities for research studies
Perform data collection and analysis
Generate study reports
Conduct literature reviews to support ongoing studies
Prepare tables, figures, and data reports for manuscripts and grants
Assist in writing research content for publications and presentations
Format and submit papers to journals
Submit IRB applications for research and quality improvement studies

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
Opportunity for annual increases based on performance
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions

Fulltime

Clinical Research Coordinator

The Ebrahimi-Fakhari Laboratory within the Movement Disorders Program in the Dep...

Location

United States , Boston

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree in neuroscience, biology, biochemistry, public health, psychology, or a related discipline required
Two years of related work experience is required for the role
Strong organizational and communication skills with attention to detail and the ability to manage multiple responsibilities in a fast-paced research environment
Experience coordinating human subject research studies or working in a clinical research environment is preferred
Familiarity with research databases (e.g., REDCap), regulatory documentation, and IRB processes is desirable
Experience working with patient populations, rare diseases, or neurological disorders is beneficial

Job Responsibility

Coordinate daily operations of clinical research studies, including scheduling and conducting study visits
Recruit and consent research participants and assist with participant screening and enrollment
Collect and manage clinical data, patient-reported outcomes, and biospecimens
Maintain accurate study documentation and regulatory binders in accordance with Good Clinical Practice (GCP) standards
Assist with Institutional Review Board (IRB) submissions, amendments, and continuing reviews
Maintain research databases (e.g., REDCap) and ensure data quality and completeness
Track study milestones, enrollment metrics, and research activities
Coordinate shipping, tracking, and documentation of research samples when applicable
Assist with coordination of multi-site research collaborations and communication with study partners
Support preparation of study materials, abstracts, reports, and progress updates for funding agencies

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

Human Subject Research Specialist I

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

Location

United States of America , Rochester

Salary:

21.36 - 29.90 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelors’ Degree Required
Or equivalent combination of education and experience Required
1- 2 years’ experience in clinical research coordination or technology research Preferred
Ability to perform and analyze basic statistical information
Knowledge of Microsoft Word, Excel and Powerpoint
Strong attention to detail and excellent interpersonal and communication skills, including writing ability

Job Responsibility

Plans, coordinates and conducts/implements all research activities associated with the development of patient and caregiver reported outcome measures, longitudinal studies and instrument translations/cultural validations
Interprets research data at the completion of each phase of instrument development and at completion of study milestones creates written summaries with tables and figures for distribution to study sponsors and for presentation at various industry events
Under the direction of the Principal Investigator, assists in the conduct of research studies beginning with the preparation of IRB materials
Coordinates subject recruitment, conducts patient interviews, programs data instrument in REDCap, implements REDCap surveys, monitors data collection within REDCap
Conducts analysis and interpretation of collected data from research studies in anticipation of validating patient and caregiver reported outcome measures
Research grant opportunities and assists with preparation of grant application materials
Assists with the preparation of study proposals for potential collaborators
Prepares grant and study sponsor milestone reports
Presents data to grant-making organizations or study sponsors as requested
Disseminates research findings by drafting abstracts, presentations, and publications for peer review and industry forums

Fulltime

Clinical Research Coordinator I

The Clinical Research Coordinator I assists principal investigators or other stu...

Location

United States , Los Angeles

Salary:

61152.00 - 100464.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

1+ year experience in clinical trial coordination or computerized databases
High School Diploma required
Bachelor's degree or Associate degree in related scientific field preferred
Certified clinical research associate/coordinator preferred

Job Responsibility

Assists principal investigators or other study team members with research studies
Assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects

Fulltime

Clinical Research Coordinator I

The Clinical Research Coordinator I assists principal investigators or other stu...

Location

United States , Los Angeles

Salary:

61152.00 - 100464.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

1+ year experience in clinical trial coordination or computerized databases
High School Diploma or GED required
Bachelor's degree or Associate degree in related scientific field preferred
Certified clinical research associate/coordinator preferred

Job Responsibility

Assists principal investigators or other study team members with research studies
Assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Human Subject Research Specialist I

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

Location

United States of America , Rochester

Salary:

21.36 - 29.90 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelors’ Degree required
Or equivalent combination of education and experience required
1- 2 years’ experience in clinical research coordination or technology research preferred
Ability to perform and analyze basic statistical information
Knowledge of Microsoft Word, Excel and Powerpoint
Strong attention to detail and excellent interpersonal and communication skills, including writing ability

Job Responsibility

Plans, coordinates and conducts/implements all research activities associated with the development of patient and caregiver reported outcome measures, longitudinal studies and instrument translations/cultural validations
Interprets research data at the completion of each phase of instrument development and at completion of study milestones creates written summaries with tables and figures for distribution to study sponsors and for presentation at various industry events
Under the direction of the Principal Investigator, assists in the conduct of research studies beginning with the preparation of IRB materials through the following activities, all within scope of approved protocol: coordinates subject recruitment, conducts patient interviews, programs data instrument in REDCap, implements REDCap surveys, monitors data collection within REDCap
Conducts analysis and interpretation of collected data from research studies in anticipation of validating patient and caregiver reported outcome measures
Researches grant opportunities and assists with preparation of grant application materials
Assists with the preparation of study proposals for potential collaborators
Prepares grant and study sponsor milestone reports
Presents data to grant-making organizations or study sponsors as requested
Disseminates research findings by drafting abstracts, presentations, and publications for peer review and industry forums
Participates in professional associations/organizations dedicated to the neurologic diseases addressed in our research

Fulltime

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