Clinical Research Analyst Job Listing at Kelly Services in Kansas City, MO (Job ID US3606423_BH9982704)

Description

Clinical Research Analyst

Kelly® Science & Clinical is seeking an experienced Clinical Research Analyst for a full-time, temporary (potential to extend/convert) opportunity with our client who has received recognition for their work in accelerating non-interventional clinical research for early cancer and chronic disease detection.

If you are passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
 

• Location: Onsite/Kansas City, MO
• Job Opportunity: Full-Time/Temporary (potential to extend/convert)
• Salary: $38.00/Hour (maximum)

Position Overview
A Clinical Research Analyst plays a critical role in the identification of qualified clinical study participants and in the collection of data required to support the development of new diagnostic and screening solutions and other medical treatments and therapies. This position requires attention to detail, a commitment to ethical research practices, and a strong ability to work in a collaborative, interdisciplinary environment.

IMPORTANT: Must have a data coordination/management background!

Responsibilities
As a Clinical Research Analyst, your primary responsibility is to support and assist in the planning, execution, and management of clinical research studies and trials. You will play a crucial role in collecting, analyzing, and interpreting data to contribute to the advancement of medical and healthcare knowledge. Your tasks will include:

• Study Planning:
• Collaborate with research teams to design and develop research protocols, including the selection of study participants, data collection methods, and study timelines.

• Data Collection & Management:
• Oversee the collection of data from clinical trials, ensuring accuracy and compliance with regulatory requirements.
• Maintain and organize study-related documents and records.
• Review potential participant s clinical records to ensure study viability.
• Ensure proper data entry within operational platforms, i.e., Electronic Data Capture EDC System and Customer Relationship Management CRM System.
• Data Analysis:
• Utilize statistical and data analysis tools to process and analyze clinical data.
• Extract meaningful insights and trends to support research objectives.
• Regulatory Compliance:
• Ensure that all research activities adhere to ethical and regulatory guidelines, such as Good Clinical Practice GCP and Institutional Review Board IRB protocols.
• Reporting:
• Prepare comprehensive reports and summaries of research findings, both for internal stakeholders and regulatory bodies.
• Contribute to scientific publications and presentations.
• Collaboration:
• Collaborate with cross-functional teams, including clinicians, researchers, and data management specialists, to facilitate the smooth execution of clinical studies.
• Quality Control:
• Implement quality control measures to guarantee the accuracy and integrity of data, identify discrepancies, and address issues promptly.
• Literature Review:
• Stay updated on current research trends, publications, and developments in the field of clinical research to inform and improve study design and data analysis.
• Technology Utilization:
• Proficiently use data management software and statistical analysis tools to support research activities.
• Communication:
• Effectively communicate research progress, challenges, and findings to the research team and other relevant stakeholders.
  Qualifications
• Bachelor s degree.
• Strong analytical and data management skills.
• Excellent communication and collaboration skills.
• Detail-oriented with a focus on data accuracy and quality.
• Familiarity with ethical and regulatory guidelines in clinical research is a plus.

 
From Bullhorn:

Clinical Research Associate III (CRA III) - A Clinical Research Analyst plays a critical role in the advancement of medical knowledge and the development of new treatments and therapies. This position requires attention to detail, a commitment to ethical research practices, and a strong ability to work in a collaborative, interdisciplinary environment. Responsibilities: As a Clinical Research Analyst, your primary responsibility is to support and assist in the planning, execution, and management of clinical research studies and trials. You will play a crucial role in collecting, analyzing, and interpreting data to contribute to the advancement of medical and healthcare knowledge. Your tasks will include: Study Planning: Collaborate with research teams to design and develop research protocols, including the selection of study participants, data collection methods, and study timelines. Data Collection and Management: Oversee the collection of data from clinical trials, ensuring accuracy and compliance with regulatory requirements. Maintain and organize study-related documents and records. Review potential participant s clinical records to ensure study viability. Ensure proper data entry within operational platforms i.e. Electronic Data Capture EDC System and Customer Relationship Management CRM System Data Analysis: Utilize statistical and data analysis tools to process and analyze clinical data. Extract meaningful insights and trends to support research objectives. Regulatory Compliance: Ensure that all research activities adhere to ethical and regulatory guidelines, such as Good Clinical Practice GCP and Institutional Review Board IRB protocols. Reporting: Prepare comprehensive reports and summaries of research findings, both for internal stakeholders and regulatory bodies. Contribute to scientific publications and presentations. Collaboration: Collaborate with cross-functional teams, including clinicians, researchers, and data management specialists, to facilitate the smooth execution of clinical studies. Quality Control: Implement quality control measures to guarantee the accuracy and integrity of data, identify discrepancies, and address issues promptly. Literature Review: Stay updated on current research trends, publications, and developments in the field of clinical research to inform and improve study design and data analysis. Technology Utilization: Proficiently use data management software and statistical analysis tools to support research activities. Communication: Effectively communicate research progress, challenges, and findings to the research team and other relevant stakeholders. Requirements: Bachelor s degree. Strong analytical and data management skills. Excellent communication and collaboration skills. Detail-oriented with a focus on data accuracy and quality. Familiarity with ethical and regulatory guidelines in clinical research is a plus.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

 Apply on company website