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JOB REQUIREMENTS: Position Description: Purpose Perform the day-to-day
administrative activities of the clinical research trials program.
Provide support to the team to facilitate the achievement of the
program\'s goals. Primary Functions Recruit, screen, enroll and obtain
consent from program participants. Conduct or coordinate training for
program participants. Coordinate research protocols including arranging
necessary appointments and procedures, working collaboratively with
other departments and institutions, and maintaining contact with study
participants. Collect, analyze, and disseminate program data. Report
program data and progress to program stakeholders. Identify problems or
obstacles in the system/procedures related to implementation of the
research protocols and communicate to the study investigators. Assure
compliance with all relevant IRB and other regulatory agency
requirements. Assist in the preparation of IRB documents and reports.
Assist in the evaluation and writing of research protocols. Collaborate
on the development of program materials including educational materials,
marketing materials, websites, forms, and reports. Work with Principal
Investigator to develop, implement, and maintain comprehensive databases
and files related to the program. Maintain program timeline including
tracking deadlines for program components. Coordinate program outreach
activities including acting as a liaison with community organizations.
Knowledge - Skills - Abilities Knowledge of biology, chemistry,
mathematics, documentation, and records management. Data utilization,
complex problem solving, critical thinking, resource management, and
writing skills. Preferred Schedule: Position Requirements:
Specifications Appropriate experience may be substituted for education
on an equivalent basis Minimum Required Education: Associate\'s Degree
Minimum Required Experience: 1 yearCertification: CITI training within
90 days of hire #LI-NI1 MCW as an Equal Opportunity Employer and
Commitment to Non-Discrimination The Medical College of Wisconsin (MCW)
is an Equal Opportunity Employer. We are committed to fostering a
diverse community of outstanding faculty, staff, and students, as well
as ensuring equal educational opportunity, employment, and access to
services, programs, and activities, without regard to an individual\'s
race, color, national origin, religion, age, disability, sex, gender
identity/expression, sexual orientation, marital status, pregnancy,
predisposing genetic characteristic, or military status. Employees,
students, applicants or other members of the MCW community For full
info follow application link. EEO/AA Minorities/Females/Vets/Disability
The Medical College of Wisconsin is an affirmative action/equal
opportunity employer and does not discriminate in hiring or employment
on the basis of age, sex, race, color, religion, national origin,
veteran status, disability or sexual orientation. APPLICATION
INSTRUCTIONS: Apply Online: ipc.us/t/FFB29B813E4A425F Qualified females,
minorities, and special disabled veterans and other veterans are
encouraged to apply.
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JOB REQUIREMENTS: Position Description: Clinical Research Coordinator
I - Diagnostic, Anesthesia, and Surgical Health (DASH) Purpose Perform
the day-to-day administrative activities of the pediatric DASH clinical
research program. Provide support to the team to facilitate the
achievement of the program\'s goals. Primary Functions Assist in the
preparation of IRB documents and reports. Assist in the evaluation and
writing of research protocols. Recruit, screen, enroll and obtain
consent from program participants. Conduct or coordinate training for
program participants. Coordinate research protocols including arranging
necessary appointments and procedures, working collaboratively with
other departments and institutions, and maintaining contact with study
participants. Collect, analyze, and disseminate program data. Report
program data and progress to program stakeholders. Identify problems or
obstacles in the system/procedures related to implementation of the
research protocols and communicate to the study investigators. Assure
compliance with all relevant IRB and other regulatory agency
requirements. Collaborate on the development of program materials
including educational materials, marketing materials, websites, forms,
and reports. Work with Principal Investigator to develop, implement, and
maintain comprehensive databases and files related to the program.
Maintain program timeline including tracking deadlines for program
components. Coordinate program outreach activities including acting as a
liaison with community organizations. Knowledge - Skills - Abilities
Knowledge of clinical research functions and regulations. Knowledge of
biology, chemistry, mathematics, documentation, and records management.
Data utilization, complex problem solving, critical thinking, resource
management, and writing skills. Preferred Schedule: Position
Requirements: Specifications Appropriate experience may be substituted
for education on an equivalent basis Minimum Required Education:
Associate\'s Degree Minimum Required Experience: 1 year Preferred
Education: Bachelor\'s Degree Preferred Experience: Experience working
in clinical research and familiarity with research protocols and
regulations. Certification: CITI training within 90 days of hire #LI-NI1
MCW as an Equal Opportunity Employer and Commitment to
Non-Discrimination The Medical College of Wisconsin (MCW) is an Equal
Opportunity Employer. We are committed to fostering a diverse community
of outstanding faculty, staff, and students, as well as ensuring equal
educational opportunity, employment, and access to services, programs,
and For full info follow application link. EEO/AA
Minorities/Females/Vets/Disability The Medical College of Wisconsin is
an affirmative action/equal opportunity employer and does not
discriminate in hiring or employment on the basis of age, sex, race,
color, religion, national origin, veteran status, disability or sexual
orientation. APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/F77858A6C4934E18 Qualified females, minorities, and special
disabled veterans and other veterans are encouraged to apply.
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Research Engagement Coordinator
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JOB REQUIREMENTS: Position Description: We are seeking a highly
motivated candidate who wants to gain experience and training in
cellular and molecular biology research on epigenomics with a focus on
translational applications in precision medicine. A qualified candidate
is expected to have excellent references from research laboratory
experience(s) and be proficient in basic molecular biology research
methods including nucleic acid preparations, protein assays, cell
culture, and more. This technologist would be involved in NIH-funded
studies focused on molecular and cellular mechanisms of epigenomic
complexes that drive cellular identities in cancer development and/or
progression, as well as inflammatory diseases. The applicant will be
encouraged to present findings weekly at lab meetings with the potential
to grow and present at national scientific conferences. As such, the
candidate should be highly motivated, self-directed, and possess
excellent communication and writing skills. Purpose Under general
direction of lab management carryout, improve and implement a variety of
laboratory techniques and specific experiments to contribute to the
timely optimization of assays and production of data in a cellular and
molecular biology research laboratory. To analyze, summarize and present
data generated to a team of scientists with ability to provide feedback
for next steps. Primary Functions With general supervision, perform
routine and complex molecular genetic methodologies including DNA/RNA
extraction, PCR/qPCR, tissue culture (sterile techniques), manipulation
of primary cultures or cell lines (introduction of exogenous DNA) and
Western blots. Be able to carry out written protocols and optimize
procedures. Independently develop and perform lab research procedures
with guidance and oversight of the laboratory team. Be able to scale
protocols and assays to large volume or sample number requests.
Participate in meetings with laboratory director/managers and research
staff. Evaluate and interpret the validity of data as necessary. Monitor
inventory, prepare media and necessary reagents for experiments, and
carry out assigned duties for maintaining supply of reagents. Operate
and perform routine maintenance on specialized equipment used in the
laboratory. Notify management or director when complex problems occur.
Create and maintain accurate records of laboratory protocols and
experimental results, ensure they are updated in a timely fashion.
Records must be available to and understandable by all staff.
Communicate summaries of research projects in individual and group
meetings. Assist in maintenance, genotyping, For full info follow
application link. EEO/AA Minorities/Females/Vets/Disability The Medical
College of Wisconsin is an affirmative action/equal opportunity employer
and does not discriminate in hiring or employment on the basis of age,
sex, race, color, religion, national origin, veteran status, disability
or sexual orientation. APPLICATION INSTRUCTIONS: Apply
Online: ipc.us/t/2285B2F3871241BC Qualified females, minorities, and
special disabled veterans and other veterans are encouraged to apply.
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Job Title: Project CoordinatorJob Description
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Research Analyst – Expert Witness Services
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Research Analyst – Expert Witness Services
