Research Associate Clinical I Jobs in Chicago Ridge, Cook, Illinois

Job Knowledge & Skills, Education, Experience

Research Associate I- Social Sciences

About The University Of Illinois Chicago

Excellent organization skills with attention to details and time management, bringing forward ideas and paths for building on organizational tools

Excellent written and verbal communication and interpersonal skills

Consistently creates pathways for process improvement, streamline workflows and build efficiently for individual and project outcomes with little guidance from manager

Works within timelines with limited oversight from manager, informing managers of any potential issues with timelines, bringing solutions/mitigations as necessary

Manage drafting and finalization of protocol and associated documents, including identifying need for amendments

Collect, manage, file and archive study documentation and correspondence. Assist in the accuracy and completeness of the Trial Master Files (TMF)

Familiar with formulas in excel and advanced database management.

Bachelors with three to five years clinical research experience.

Strong oral and written communication skills in order to address large/diverse audiences. Strong customer service skills required.

Intermediate knowledge of Microsoft Office Suite (Excel, Work, Outlook, etc.).

Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred.

Works collaboratively with all levels within the organization to advise on contractual negotiations, recommendations and processes.

Perform independent literature reviews or background research to become familiar with technical knowledge needed for this role.

Knowledge of fundamental research concepts, practices and procedures.

Entry level knowledge of research methods.

Strong writing and verbal communication skills

Experience or background in biology, restoration ecology, or related fields is a plus

Perform technical reviews of program applications and other documentation provided by industry participants.

Visiting Research Associate I - HCHS/SOL

About the University of Illinois Chicago

Required Employment Notices and Posters

The university provides accommodations to applicants and employees.

M-F; working remotely from home, Midwest USA-based location, near a major airport; travel routinely 50-60% and up to 80% at times.

Bachelor's degree in a science or healthcare-related field or a registered nursing certification or equivalent certification/licensure from an appropriately accredited institution.

3 years of CRC experience or previous 1-year experience as a CRA.

Direct patient care or clinical research experience required.

Familiarity with clinical research and study development processes.

Valid Driver's License where applicable.

Understand and apply applicable corporate and divisional SOPs. Maintain knowledge of relevant QSR and safety requirements.

Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks.

Develop knowledge and understanding of GxP and related regulations and guidance.

Bachelors degree in a science-related field with 0-1 years experience

Possess relevant laboratory (chemistry)/technical, writing, and computer skills.

Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction.

Oversee site management responsibilities for assigned sites.

Assist in the management of routine trial activities, adhering to industry and corporate standards.

Support the Study Team/Management in all phases of the clinical trial.

Manage trial-specific Trial Master File (TMF) and internal filing system, including regulatory and legal document tracking and archiving.

2+ years of experience in a sponsor or CRO setting (strongly preferred).

Knowledge of clinical research in Cardiology/Medical Devices

Must be detail-oriented and efficient in time management.

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff.

Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and

Basic knowledge in regulations for applicable geographies and types of studies (IDE, non-significant risk, feasibility, exempt, etc.).

Minimum 1-year clinical research experience required.

College/University degree in Life Sciences or an equivalent combination of education, training & experience

Communication, collaboration, and problem-solving skills

To act as the main point of communication with Investigator and his team

When requested to support preparation of regulatory and / or EC submission

Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance

Full working proficiency in English

College/University degree in Life Sciences or an equivalent combination of education, training & experience

Communication, collaboration, and problem-solving skills

To act as the main point of communication with Investigator and his team

When requested to support preparation of regulatory and / or EC submission

Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance

Full working proficiency in English

Collaborate with Data Manager and/or Clinical Affairs management to define data management plan and design CRFs.

Computer software skills (e.g., MS Word, Excel, PowerPoint and Google products experience).

Knowledge of FDA requirements for clinical validation and CLIA waiver.

Minimum 3 years of related experience, preferably including clinical research and clinical operations experience.

Experience working in IVD clinical studies highly preferred.

Strong attention to detail, self-motivation, and good organizational skills.

At least two years of experience as a clinical research associate

Excellent writing, editing, and communication skills

Strong Administrative and Organizational skills to support several team members

A bachelors degree in Health Sciences, Nursing or Medical Biotechnology, or Biological Sciences

Familiarity with various computer document formats, styles, and standards

· Collecting, analyzing, and recording data

The Clinical Research Intern will apply analytical, project management skills and enthusiasm for healthcare and commitment to improving healthcare through research.

The candidate will Product practical experience within the Clinical Research operations at ***.

Complies with established policies, health and safety regulations and requirements, procedures, and department objectives.

Bachelor's Degree in biological or life sciences or health related field OR attending/completed a clinical research certification program.

Proficient computer skills using Microsoft Office products.

May assist with follow up and closing of clinical studies.

Able to manage multiple and competing priorities through effective organizational management skills.

Effective interpersonal skills; able to build effective relationships with study management team colleagues and business partners.

Excellent time management skills; able to accomplish established goals efficiently.

Supply chain management support may include:

Support Trial Management team member with assigned study specific projects and tasks.

Two years Clinical Research work experience, or relevant experience

Clinical Trial Collaboration: Work alongside our clinical team, focusing on site qualification, initiation, management, and data integrity.

Data Management: Oversee data activities, generate, and resolve queries, and report on study metrics including enrollment and adverse events documentation.

Regulatory Oversight: Manage investigational product accountability, monitor IRB requirements, and ensure prompt processing of regulatory documents.

Bachelor’s degree in a medical/scientific field, with 4+ years of clinical research experience (Master’s degree can substitute for 1 year).

Strong organizational, multitasking, and relationship-building abilities.

Effective communication skills and keen attention to detail.

Conduct all types of visits including, qualification, initiaiton, monitoring and close out

Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff

Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements

Minimum 1.5 years monitoring experience

Strong verbal and written communication skills

8-12 days on site per month

5+ years of CRA experience.

3+ years of experience working on oncology studies.

BS in a relevant scientific discipline.

Ability to travel and be on-site. (Austin, TX or Portland, OR).

6-month contract. - 40 hours per week. - Monday to Friday.

Austin, TX or Portland, OR

Excellent interpersonal, oral, and written communication skills in English

Superior organizational skills with attention to details

5+ years of experience as a Clinical Research Associate

Experience in CNS is required

Conduct study initiation visits (SIVs)

Ability to work with little or no supervision

Required Knowledge, Skills, And Abilities

Assists with the preparation of summary documents and reports in conjunction with Program Manager and Project Manager.

Strong communication, qualitative and quantitative analytical skills.

Experience within Health Services Research preferred.

Experience in biostatistics and epidemiology.

Minimum of 0-2 years' experience required.

Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.

Demonstrated knowledge of how to synthesis study conduct.

Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.

Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.

Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.

Knowledge of clinical trials records, procedures, and computerized data processing systems. Demonstrated knowledge of how to synthesize study conduct.

Ability to multi-task and have good organizational and time management skills.

Experience in clinical research or the medical field preferred

Experience with Electronic Data Capture (EDC) systems, for the purpose of clinical research, preferred.

Experience with programming and coding (e.g., HTML and Java) required.

Possess excellent written and oral communication skills.

Critical thinking and problem-solving skills

Must have 1-3 years experience with molecular and in vivo techniques.

Must have experience with mouse colony maintenance.

Responsibilities of the Research Associate I/II:

Requirements of the Research Associate I/II:

Will perform and/or coordinate a wide range of highly sophisticated laboratory techniques to analyze the functions of immunoregulatory pathways.

Responsible for T cell function, cytokine ELISA assays, and multiparameter flow cytometry).

Minimum of four (4) years of experience in clinical research specifically in Ophthalmology surgical medical devices.

Experience in glaucoma devices is strongly preferred.

Knowledge of medical and ophthalmology terminology

Remotely monitor data and support clinical sites for protocol compliance and recruitment activities

Manage clinical trial close-out activities, including return of investigational product, final reconciliation of all required documentation, and EDC close-out

** Candidates must have experience in Ophthalmology Clinical Research trials to be considered!

Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently

Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources

Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.

Demonstrated knowledge of how to synthesis study conduct.

Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.

Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.

Bachelor’s degree plus 3-5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or

Associate’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or

High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection

Bachelor’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management and data collection

Knowledge and skill with word processing, spreadsheet, database, and e-mail computer software (e.g., Microsoft Word, Excel, Access, Outlook)

UAMS offers amazing benefits and perks

• Maintains on-going professional education on clinical trials and research

• Minimum requirement: master’s degree in nursing/Healthcare related field

• Clinical work experience in oncology

• Excellent organizational and communications skills, with team-player proven ability to meet project deadlines

• Knowledge of data analytics

• Serves as a liaison to industry sponsored, consortium and Investigator initiated Brain Tumor Trials

Basic knowledge of analytical chemistry methods Sincere interest in translating basic research insights into impactful therapeutics

Operate and maintain robotic systems for high-throughput assays.

Conduct physicochemical property assays, including but not limited to logD, pKa, and stability tests.

Collect, analyze, and interpret data generated from assays, ensuring high-quality and reliable results.

Maintain accurate and up-to-date records of all experiments and findings.

Assist in troubleshooting equipment and experimental problems.