Research Associate Clinical I Jobs in Bowie, Texas

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).

Develop skills in project coordination, data management, and regulatory compliance

Gain experience in conducting clinical research in a multi-center setting

Manage a central clinical database, biobanking of biosamples, and a genome archive

Prior experience in clinical research is preferred but not required

Strong organizational and communication skills

Engage in close collaboration with patients and families, particularly in the context of rare diseases

Knowledge of scripting and/or programming languages.

Previous experience providing user support in a clinical research environment desired.

Delivering technical solutions that meet user needs in the required timeframe, prioritizing effectively for assigned scope of work

Applying acquired expertise to analyze and solve technical problems without clear precedent

Providing technical guidance to employees, colleagues and customers

Delivering a high level of customer service as per agreed-upon metrics.

One year of relevant work experience is preferred.

Analytical skills to gather and interpret data in which the information or problems are moderately complex to complex.

Working alongside Investigators and collaborators to assist in the start-up and conduct of studies;

Participating in the development of study manuals and other study-related documents;

Assisting the Research Coordinators with IRB applications, preparing amendments and continuing reviews for each study and for each participating site;

Facilitating the scheduling and organizing of calls with Investigators, Research Coordinators and Vendors as needed;

Evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study.

Monitor and reviews data collection and data entry, and informed consent procedures ensuring consistency of application for each study.

Analytical skills to gather and interpret data in which the information or problems are moderate to complex.

Consent and recruit patients for research studies through personal interviews and written communications with patients/families.

Provide details to families with detailed background information regarding studies communicate all policies and procedures, and respond to all inquiries.

Coordinate follow-up visits as necessary.

High degree of computer literacy and ability/willingness to learn basic website management skills. Coding skills highly desirable.

Knowledge of data management programs.

Working in concert with Principal Investigator and/or Research Manager, develops and implements patient recruitment strategies.

Assists PI or Research Manager with preparation for presentation and written published articles; there are opportunities to communicate research to colleagues.

Prior experience in the clinic or clinical research is highly desired.

At least one year of work experience in a research setting. Sound independent judgment and competence in research methodologies.

Experience with clinical/psychological research, including recruiting research participants and using electronic data management software.

Working knowledge of literature searches & using reference management software

Assisting with literature reviews and reference management for grant submissions

Experience with PowerPoint and Excel.

Experience with data collection, preferably in clinical setting.

Prior experience working or volunteering in a large, academic research center.

Evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study.

Monitor and review data collection, data entry, and informed consent procedures, ensuring consistency of application for each study.

Consent and recruit patients for research studies through personal interviews and written communications with patients/families.

Provide detailed background information regarding studies to families, communicate all policies and procedures, and respond to all inquiries.

Coordinate follow-up visits as necessary.

Act as a resource to study participants, addressing their concerns.

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

Experience performing molecular, biochemical, and cell biology techniques, including PCR, qPCR, RT-PCR, gel electrophoresis, cloning, nucleic acid purification etc.

Excellent communication skills, both verbal and written.

Knowledge of Microsoft Office products.

Assist in experimental design and independently conduct scientific experiments for product development, performance troubleshooting, and protocol optimization

Develop and write project protocols and methodology for developed research components.

Discuss and analyze experiments with the Principal Investigator

Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.

Participate in maintaining accuracy within clinical management systems and internal reports and trackers.

Able to manage multiple projects independently and use varying databases and management systems.

Minimum 1-3 years relevant clinical research experience.

Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.

Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.

Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.

Performs related approved responsibilities as required.

(1.) High School Diploma or GED and three years of administrative support experience OR

(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR

Handles or assists with administrative activities generally associated with the conduct of clinical trials.

Assists with patient recruitment. Attends study meetings.

Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software

Bachelors degree or equivalent work experience required

2-4 years experience in clinical research preferred

2-4 years non-profit, research, or healthcare experience desired

Knowledge of CFR, GCP and ICH guidelines

Promote safety and confidentiality of research participants at all times

Conduct and oversee data collection and management; help generate study reports

Help prepare research materials (such as study protocols, questionnaires, educational materials, and data collection instruments)

High level of attention to detail, excellent organizational skills.

Excellent written skills, including academic writing skills. Outstanding interpersonal and verbal communication skills.

Strong working knowledge of Microsoft Office applications, specifically Word, Excel, PowerPoint, and Outlook.

Experience working with qualitative and quantitative data collection and analysis.

Participating in the daily activities and work assignments of research staff.

Planning and coordinating complex research experiments following standard operating procedures.

Working with Principal Investigator(s) to coordinate project activities and establish appropriate reporting procedures.

Contributing to scientific analysis and interpretation of projects.

Establishing and maintaining quality control measures for assigned project operations.

Making modifications to research procedures in collaboration with the Principal Investigator(s) and contributing to the writing of SOPs and protocols.

Improve the health and well-being of individuals and communities;

Increase the diversity of the health professional and scientific workforce;

You will find a fulfilling career at

Two years of relevant experience.

Supports daily operations for a research study or clinical trial.

Recruits, screens, and enrolls study participants; ensures participant adherence to study protocol.

Collects, evaluates, enters, and tracks data.

Submits data, study documents, and/or reports to regulatory agencies.

Assists with completion of protocol-specific documents.

Excellent time management skills and ability to work independently with minimal direction

0 - 3 years molecular biology or biochemistry laboratory experience post-BS/MS degree

3+/0+ years molecular biology or biochemistry laboratory experience post-BS/MS degree

Good understanding and hands on experience in biological sample handling, nucleic acid purification, amplification and detection techniques

Demonstrated working knowledge of scientific principles

Excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple changing projects and priorities

May collect, secure and assist with biospecimen management.

Must be able to work in a Labor/Management Partnership environment.

Adheres to compliance and privacy/ confidentiality requirements and standards.

Acquires and maintains knowledge of KP systems and databases.

Minimum one (1) year of experience in public health, healthcare administration, epidemiology, or healthcare-related field.

High School Diploma or General Education Development (GED) required.