161 Researchers jobs in St. Louis
Graduate Trainee - Data Analysis
63101 St. Louis, Missouri
$45000 Annually
WhatJobs
Posted 21 days ago
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Job Description
Our client is offering an exceptional opportunity for bright and motivated graduates to join their esteemed organization as Graduate Trainees specializing in Data Analysis in St. Louis, Missouri, US . This comprehensive program is designed to provide recent graduates with hands-on experience and mentorship to build a strong foundation in data science and analytics. You will work closely with experienced data analysts and scientists on real-world projects, gaining exposure to data collection, cleaning, processing, and visualization techniques. Key responsibilities will include assisting in the development of analytical models, conducting statistical analysis, and generating insightful reports to support business decision-making. You will have the opportunity to learn and utilize various data analysis tools and programming languages such as Python, R, SQL, and Tableau. The ideal candidate possesses a strong quantitative aptitude, excellent problem-solving skills, and a keen interest in extracting meaningful insights from data. A recent Bachelor's or Master's degree in a quantitative field such as Statistics, Mathematics, Computer Science, Economics, or a related discipline is required. Strong communication and teamwork abilities are also essential. This is a fantastic entry-level position for aspiring data professionals looking to launch their careers in a supportive and innovative environment. Gain invaluable practical experience and contribute to impactful data-driven initiatives. Our client is committed to fostering talent and providing a clear career path for its trainees.
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0
Research Associate
63101 St. Louis, Missouri
Federal Reserve Bank (FRB)
Posted 13 days ago
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Job Description
Company Federal Reserve
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1
Advanced AI Research Scientist Associate Manager
63112 Saint Louis, Missouri
Accenture
Posted 11 days ago
Job Viewed
Job Description
We Are
Accenture is helping companies use generative AI to reinvent their enterprise and optimize business functions for breakthrough innovation and competitive advantage. With over 1,600 professionals dedicated to generative AI, leveraging the depth and experience of more than 40,000 AI and data professionals across the company our Generative AI and LLM Center of Excellence ( brings together our Experienced Innovation, Strategic Investment, Exceptional Talent, and Power Ecosystem.
You Are
As an Advanced AI Research Scientist, you formulate real-world problems into practical, efficient, and scalable AI and Machine Learning problems.
+ You lead a team and provide guidance to explore and implement new methodologies, model building techniques, and cutting-edge algorithms, and applying these techniques with the right architecture to solve real-world problems.
+ You have a deep understanding and ability to remain at the forefront of generative AI, LLM, and multi-modal models (with a focus on driving innovation by applying these techniques to new business problems, use cases, and scenarios).
+ As needed by the specific problem, you train and/or fine-tune generative AI models and evaluate on the specific problem.
+ As a significant part of this role, you will be justifying the value of innovative generative AI or traditional Machine Learning approaches (or a combination of both) in the business problems, and you'll be expected to construct methodologies that clearly demonstrate their value.
+ You'll also work collaboratively with teams from both the business and technical side, including users, use case representatives, business owners, engineers, architects, and UI designers, to achieve end-to-end project development goals.
The Work
+ Participate internal and external discussions to gather business use case requirements, provide on the spot AI expertise and AI solution options for business problems.
+ Design, develop and implement advanced AI/ML models, especially LLM and other Gen AI models from scratch or existing foundation models via self-supervised learning, transferred-learning, and fine-tuning techniques.
+ Design, develop and implement highly sophisticated Gen AI based applications including generative agent and similar architectures which support multiple Gen AI models to work together for complex tasks.
+ Lead technical teams and grow true AI expertise within broader team including offshore
+ Collaborate seamlessly with diverse, cross-functional teams to accurately identify and prioritize requirements, ensuring that the AI solutions meets the needs and expectations of various stakeholders.
+ Develop and execute an AI solution project plan with team, timeline, and infrastructure dependency.
+ Define and implement a value justification approach to the AI solutions; estimate solution cost with right technological choices; and calculate ROI.
+ Create and maintain comprehensive technical documentation that comprehensibly captures the intricate details of the solution, capture IP, facilitating seamless understanding, knowledge
Accenture is helping companies use generative AI to reinvent their enterprise and optimize business functions for breakthrough innovation and competitive advantage. With over 1,600 professionals dedicated to generative AI, leveraging the depth and experience of more than 40,000 AI and data professionals across the company our Generative AI and LLM Center of Excellence ( brings together our Experienced Innovation, Strategic Investment, Exceptional Talent, and Power Ecosystem.
You Are
As an Advanced AI Research Scientist, you formulate real-world problems into practical, efficient, and scalable AI and Machine Learning problems.
+ You lead a team and provide guidance to explore and implement new methodologies, model building techniques, and cutting-edge algorithms, and applying these techniques with the right architecture to solve real-world problems.
+ You have a deep understanding and ability to remain at the forefront of generative AI, LLM, and multi-modal models (with a focus on driving innovation by applying these techniques to new business problems, use cases, and scenarios).
+ As needed by the specific problem, you train and/or fine-tune generative AI models and evaluate on the specific problem.
+ As a significant part of this role, you will be justifying the value of innovative generative AI or traditional Machine Learning approaches (or a combination of both) in the business problems, and you'll be expected to construct methodologies that clearly demonstrate their value.
+ You'll also work collaboratively with teams from both the business and technical side, including users, use case representatives, business owners, engineers, architects, and UI designers, to achieve end-to-end project development goals.
The Work
+ Participate internal and external discussions to gather business use case requirements, provide on the spot AI expertise and AI solution options for business problems.
+ Design, develop and implement advanced AI/ML models, especially LLM and other Gen AI models from scratch or existing foundation models via self-supervised learning, transferred-learning, and fine-tuning techniques.
+ Design, develop and implement highly sophisticated Gen AI based applications including generative agent and similar architectures which support multiple Gen AI models to work together for complex tasks.
+ Lead technical teams and grow true AI expertise within broader team including offshore
+ Collaborate seamlessly with diverse, cross-functional teams to accurately identify and prioritize requirements, ensuring that the AI solutions meets the needs and expectations of various stakeholders.
+ Develop and execute an AI solution project plan with team, timeline, and infrastructure dependency.
+ Define and implement a value justification approach to the AI solutions; estimate solution cost with right technological choices; and calculate ROI.
+ Create and maintain comprehensive technical documentation that comprehensibly captures the intricate details of the solution, capture IP, facilitating seamless understanding, knowledge
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2
Senior Clinical Research Associate
63101 St. Louis, Missouri
$95000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a highly skilled and experienced Senior Clinical Research Associate (CRA) to join their esteemed team in **St. Louis, Missouri, US**. This critical role involves overseeing and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, company policies, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring the quality and integrity of the data collected.
Key responsibilities include:
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field, or equivalent experience. A Master's degree is a plus. A minimum of 5 years of experience as a Clinical Research Associate, with a proven track record of successful clinical trial management, is required. In-depth knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA) is essential. Experience with various therapeutic areas is advantageous. Excellent organizational, communication, and interpersonal skills are necessary. The ability to travel as required to clinical sites is a must. Strong problem-solving skills and the ability to work independently and as part of a team are crucial for success in this role within **St. Louis, Missouri, US**.
Key responsibilities include:
- Conducting site visits (initiation, interim monitoring, and close-out) to assess study compliance and data quality.
- Ensuring adherence to study protocols, GCP guidelines, and applicable regulatory requirements.
- Monitoring subject recruitment and retention efforts at clinical trial sites.
- Verifying the accuracy and completeness of source data and case report forms (CRFs).
- Managing and resolving site-level issues and deviations.
- Building and maintaining strong relationships with investigators and study site staff.
- Preparing and presenting study progress reports to project teams and management.
- Ensuring timely submission of essential documents to regulatory authorities and IRBs/ECs.
- Providing training and guidance to study site personnel.
- Managing clinical trial supplies and equipment at investigator sites.
- Contributing to the development of clinical trial protocols and study plans.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field, or equivalent experience. A Master's degree is a plus. A minimum of 5 years of experience as a Clinical Research Associate, with a proven track record of successful clinical trial management, is required. In-depth knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA) is essential. Experience with various therapeutic areas is advantageous. Excellent organizational, communication, and interpersonal skills are necessary. The ability to travel as required to clinical sites is a must. Strong problem-solving skills and the ability to work independently and as part of a team are crucial for success in this role within **St. Louis, Missouri, US**.
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3
Clinical Research Associate (Pharmaceutical)
63105 St. Louis, Missouri
$85000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in St. Louis, Missouri, US . This role is pivotal in supporting the execution of clinical trials, ensuring adherence to study protocols, regulatory requirements, and good clinical practices (GCP). You will be responsible for site selection, initiation, monitoring, and close-out visits for clinical trial sites. Key duties include verifying data accuracy, ensuring patient safety, managing trial documentation, and resolving site-specific issues. This hybrid position involves travel to clinical sites (approximately 50-60%) combined with remote work for data review and administrative tasks. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A minimum of 3 years of experience as a CRA or in a similar clinical research role is required. In-depth knowledge of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational skills, strong attention to detail, and exceptional communication abilities are paramount. You must be proficient in clinical trial management software and possess a valid driver's license. This is a challenging yet rewarding opportunity to contribute to the development of life-saving medications and advance your career in the pharmaceutical industry. Join our client and be part of a scientific endeavor that impacts global health.
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4
Clinical Research Associate (CRA)
63101 St. Louis, Missouri
$95000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their team in St. Louis, Missouri, US . This critical role involves overseeing and managing clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as performing source data verification, reviewing regulatory documents, and ensuring the accuracy and completeness of trial data. Building and maintaining strong relationships with investigators, site staff, and internal project teams is essential for the successful execution of clinical trials. You will also be responsible for identifying and resolving site-specific issues, providing training to site personnel, and ensuring timely reporting of study progress and adverse events. The ideal candidate will possess a bachelor's degree in a life science, nursing, or a related field. A minimum of 3 years of experience as a CRA or in a similar clinical research role is required, with a strong understanding of drug development processes and clinical trial management. Excellent knowledge of ICH-GCP guidelines and regulatory requirements (FDA, EMA) is essential. Strong organizational, analytical, and problem-solving skills, along with exceptional communication and interpersonal abilities, are necessary. The ability to travel frequently (up to 60%) to clinical trial sites is a requirement for this position. This is an exceptional opportunity to contribute to the advancement of life-saving therapies and build a rewarding career within a leading pharmaceutical organization.
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5
Clinical Research Associate - Oncology
63103 St. Louis, Missouri
$95000 Annually
WhatJobs
Posted 7 days ago
Job Viewed
Job Description
Our client, a leading biopharmaceutical company, is looking for an experienced Clinical Research Associate (CRA) with a specialization in Oncology to join their dynamic team in St. Louis, Missouri, US . This critical role involves overseeing and managing clinical trials from initiation to close-out, ensuring adherence to Good Clinical Practice (GCP), FDA regulations, and study protocols. You will be responsible for site selection, initiation visits, monitoring site performance, ensuring data integrity, and managing drug accountability. The ideal candidate will have a strong background in oncology drug development, with a proven track record of successfully managing Phase I-III clinical trials. A Bachelor's degree in a life science, nursing, or a related field is required; an advanced degree is preferred. Minimum of three years of experience as a CRA, with at least two years focused on oncology studies, is essential. Excellent understanding of ICH-GCP guidelines and regulatory requirements is paramount. Strong organizational skills, attention to detail, and the ability to travel (approximately 50-60%) to clinical sites are necessary. You will work closely with investigators, study coordinators, and internal study teams to ensure timely and accurate data collection and reporting. This position offers a competitive salary, comprehensive benefits package, and opportunities for professional growth within a cutting-edge research environment. If you are passionate about advancing cancer treatments and possess the required expertise, we encourage you to apply.
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6
Clinical Research Associate (Remote)
63103 St. Louis, Missouri
$75000 Annually
WhatJobs
Posted 10 days ago
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Job Description
We are looking for a dedicated and experienced Clinical Research Associate (CRA) to join our client's dynamic pharmaceutical team, operating in a fully remote capacity. This role is critical in ensuring the quality, integrity, and compliance of clinical trial data across various therapeutic areas. As a remote CRA, you will be responsible for monitoring clinical trial sites, ensuring adherence to protocols, GCP, and regulatory requirements. Your duties will include pre-trial monitoring visits, initiation visits, routine monitoring visits, and close-out visits, all conducted remotely or with occasional travel as needed. You will meticulously review study-related source documents, verify data accuracy and completeness, and ensure that all trial activities are conducted in accordance with the study plan and applicable regulations. Additionally, you will build and maintain strong relationships with investigators and site staff, providing them with the necessary support and guidance throughout the trial. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of direct CRA experience. Strong understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements is essential. Excellent organizational, communication, and interpersonal skills are paramount for success in this role, as is the ability to work independently and manage your time effectively in a remote setting. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is required. This is a fantastic opportunity to contribute to groundbreaking research while enjoying the flexibility of a remote work arrangement. If you are passionate about advancing pharmaceutical development and possess the requisite skills and experience, we invite you to apply and become a vital part of our client's mission. This fully remote position offers a competitive salary, comprehensive benefits, and the chance to make a significant impact on patient health. We are based in St. Louis, Missouri, US , but this role is remote.
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7
Senior Clinical Research Associate
63101 St. Louis, Missouri
$110000 Annually
WhatJobs
Posted 13 days ago
Job Viewed
Job Description
Our client, a renowned pharmaceutical company at the forefront of medical innovation, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dedicated team in St. Louis, Missouri . This is an on-site position requiring a strong presence within our research facilities. As a Senior CRA, you will be responsible for ensuring the quality, integrity, and compliance of clinical trials according to Good Clinical Practice (GCP) guidelines and regulatory requirements. You will play a vital role in managing all aspects of clinical trial site management, from site selection and initiation to monitoring, close-out, and data verification. Your meticulous attention to detail and commitment to ethical research practices will be critical in advancing life-changing therapies.
Key Responsibilities:
Key Responsibilities:
- Perform site initiation, monitoring, and close-out visits in accordance with study protocols and GCP.
- Ensure accurate and timely collection of clinical data, source document verification, and query resolution.
- Maintain effective communication with clinical trial sites, investigators, and study personnel.
- Oversee the safety reporting process and ensure adherence to protocol and regulatory requirements.
- Manage study supplies and investigational product at clinical sites.
- Prepare and present study progress updates to internal stakeholders and study teams.
- Ensure compliance with all applicable regulatory requirements and company policies.
- Mentor and provide guidance to junior CRAs as needed.
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in site management, monitoring, and data review.
- Excellent organizational, communication, and interpersonal skills.
- Ability to travel as required for site visits and meetings.
- Strong computer skills, including proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Detail-oriented with a strong commitment to data accuracy and integrity.
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8
Senior Clinical Research Associate
63101 St. Louis, Missouri
$95000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled Senior Clinical Research Associate (CRA) to join their expanding team in St. Louis, Missouri . This critical role supports the planning, implementation, and execution of clinical trials, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out activities, meticulously tracking patient recruitment, data integrity, and site compliance. You will serve as the primary liaison between the investigative sites and the clinical operations team, providing essential support and guidance to study personnel. This position requires a meticulous approach to documentation and a deep understanding of clinical trial management processes.
Key Responsibilities:
Key Responsibilities:
- Conduct pre-study, interim, and close-out site visits to assess eligibility, review regulatory documents, and ensure data accuracy and integrity.
- Monitor study progress, identify potential issues, and implement corrective actions to ensure study milestones are met.
- Train and mentor investigative site staff on protocol requirements, study procedures, and regulatory compliance.
- Ensure all clinical trial documentation is maintained in accordance with company SOPs and regulatory standards.
- Collaborate with investigators and site staff to resolve data discrepancies and query resolution.
- Prepare site monitoring reports and communicate findings to the clinical trial team.
- Contribute to the development of study-related documents, including protocols and case report forms.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
- Minimum of 4-6 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements (FDA, EMA).
- Demonstrated experience in clinical trial monitoring and site management.
- Excellent communication, interpersonal, and organizational skills.
- Ability to travel up to 60% to investigative sites.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
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9