Research Associate Clinical I Jobs

Job Knowledge & Skills, Education, Experience

Research Associate I- Social Sciences

About The University Of Illinois Chicago

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.

B.S. in a biology discipline (Biology, Neuroscience, Bioengineering), 0-2 years of industry experience

Experience in mammalian cell culture

Experience in DNA/RNA extraction, PCR/qPCR, ELISA, western blot, immunostaining

Effective verbal and written communication skills relating to colleagues and associates inside and outside the organization.

Maintain cell lines (hiPSCs/HEK/Glia cell) with sterile techniques.

Support and collaborate with scientists, labs, vendors, and industry experts to ensure the completion of tasks/projects.

Good understanding of Clinical Study Management including monitoring, study drug handling and data management

1.5+ years of CRA experience in Cardiovascular/Metabolic, Respiratory and/or Immunology therapeutic experience

Fluent knowledge of spoken and written English

Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP

Good knowledge of relevant local regulations

Good medical knowledge in relevant AZ Therapeutic Areas

7. Assists investigator with correspondence with IRB. (essential)

4. Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.

3. Potential exposure to adverse environmental conditions

o Several times a month: Radiation-irradiator possible.