186 Researchers jobs in St. Louis

Job Title: Clinical Research Associate/Coordinator
20 Hours Per Week- will be travel during core buisness hours
Job Description
We are seeking a Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), or Clinical Nursing Coordinator (CNC) with 2-4 years of clinical experience to join our team. The primary focus of this role is to enter data for screening, surgery, and end-of-study into EPIC and Open Clinica. This position is pivotal in supporting our 2A lung cancer study, which involves an innovative imaging agent used during surgeries.
Responsibilities
+ Enter screening data on the day of surgery, post-surgery, and at the end of the study into EPIC and Open Clinica.
+ Support 2-4 surgeries per month for a year, with approximately 35 patients enrolled.
+ Travel for surgeries, primarily in the Philadelphia area, with additional locations in Texas, Iowa, and Colorado.
+ Attend surgeries, enter data before, during, and after surgery, and debrief with onsite team members.
+ Transcribe data remotely within three days post-surgery.
+ Be available for travel on short notice if required.
Essential Skills
+ 2-4 years of clinical experience.
+ A four-year degree in Sciences or Nursing.
+ Proficiency in data entry and clinical research software such as EPIC and Open Clinica.
Additional Skills & Qualifications
+ Experience in oncology is desirable but not required.
+ Flexibility to be cross-trained or handle TMF, medical writing, and study reports.
+ Must complete a credentialing process, including online training and a background check.
Work Environment
This position involves both remote work and onsite attendance at surgical sites. Travel is required, with the possibility of day trips for Philadelphia surgeries and overnight stays for other locations. The role demands flexibility, as the schedule may vary, and consultants should be prepared to travel by car or flight. Consultants will use their own laptop and cell phone; however, a laptop can be provided if necessary.
Job Type & Location
This is a Contract position based out of Chesterfield, Missouri.
Pay and Benefits
The pay range for this position is $45.00 - $57.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a hybrid position in Chesterfield,MO.
Application Deadline
This position is anticipated to close on Oct 22, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Our client, a leading pharmaceutical innovator, is seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join their dynamic team in **St. Louis, Missouri, US**. The CRA plays a critical role in ensuring the smooth execution of clinical trials, adhering strictly to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. This position involves frequent site visits, data verification, and close collaboration with investigators and study staff to maintain data integrity and patient safety.

Responsibilities:

• Monitor clinical trial sites to ensure adherence to protocols, regulatory requirements, and company policies.
• Verify accuracy, completeness, and validity of clinical trial data through source data verification (SDV).
• Conduct site initiation, interim monitoring, and close-out visits according to study plans.
• Manage study sites, providing training and ongoing support to investigators and site staff.
• Ensure proper documentation and maintenance of regulatory files at study sites.
• Identify, assess, and resolve issues that may impact study conduct or data quality.
• Communicate effectively with study teams, investigators, and internal stakeholders regarding site performance and study progress.
• Prepare and submit monitoring reports in a timely and accurate manner.
• Contribute to the development of study-related documents, such as protocols, informed consent forms, and case report forms (CRFs).
• Ensure compliance with all applicable local and international regulations (e.g., FDA, EMA).
• Participate in the selection and qualification of new study sites.
• Uphold the highest ethical standards in all aspects of clinical research.

Qualifications:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
• Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
• Proven experience in site monitoring, including initiation, routine, and close-out visits.
• Strong ability to interpret clinical trial protocols and identify deviations.
• Excellent written and verbal communication skills, with the ability to document findings clearly and concisely.
• Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Strong organizational and time management skills, with the ability to manage multiple sites and tasks simultaneously.
• Willingness to travel up to 60% of the time to monitor clinical sites.
• Problem-solving skills and the ability to make sound decisions.
• High attention to detail and commitment to data accuracy.

This hybrid role offers a competitive salary, comprehensive benefits, and the chance to contribute to groundbreaking pharmaceutical advancements.

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.
Join our AI Talent Community ( to stay up-to-date on job opportunities, events and news!
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 transfer and future development.
+ Collaborate with academia partners to stay on the cutting edge of AI, especially Gen AI technologies, provide through leadership on AI trend, AI use case innovation trend, new AI opportunities, or foreseeable limitation, risks, and concerns.
Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements.
This role requires working onsite at our Generative AI Center of Excellence located in Mountain View, CA.
Here's What You Need
+ Minimum of 4 years of experience in designing and developing neural network models, especially deep learning model, and Foundation models.
+ Minimum of 4 years of experience of experience in building, fine-tuning Foundation models including LLMs and multi-modal models.
+ Minimum of 4 years of strong working knowledge of the different technologies, their differences, modalities in the Generate AI space.
+ Minimum of 4 years of working knowledge and familiarity with different LLM driven application architecture patterns.
+ Minimum of 4 years of experience in deep learning and neural networks, in particular training and large language models with popular libraries and GPUs.
+ Minimum of 4 years of working knowledge of computer architecture, and familiarity with the fundamentals of GPU architecture.
+ Minimum of 4 years of proven experience with processor and system-level performance modelling.
+ Minimum of 2 years of experience of technical team management or team mentoring.
+ Bachelor's degree or equivalent (minimum 12 years) work experience. (If Associate's Degree, must have minimum 6 years' work experience)
Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below.We accept applications on an on-going basis and there is no fixed deadline to apply.
Information on benefits is here. ( Location Annual Salary Range
California $73,800 to $20,400
Cleveland 68,300 to 176,300
Colorado 73,800 to 190,400
District of Columbia 78,500 to 202,700
Illinois 68,300 to 190,400
Maryland 73,800 to 190,400
Massachusetts 73,800 to 202,700
Minnesota 73,800 to 190,400
New York/New Jersey 68,300 to 220,400
Washington 78,500 to 202,700
#LI-NA-FY25
Requesting an Accommodation
Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired.
If you would like to be considered for employment opportunities with Accenture and have accommodation needs such as for a disability or religious observance, please call us toll free at or send us an email or speak with your recruiter.
Equal Employment Opportunity Statement
We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities.
For details, view a copy of the Accenture Equal Opportunity Statement ( is an EEO and Affirmative Action Employer of Veterans/Individuals with Disabilities.
Accenture is committed to providing veteran employment opportunities to our service men and women.
Other Employment Statements
Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States.
Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration.
Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process. Further, at Accenture a criminal conviction history is not an absolute bar to employment.
The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Additionally, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the Company's legal duty to furnish information.
California requires additional notifications for applicants and employees. If you are a California resident, live in or plan to work from Los Angeles County upon being hired for this position, please click here for additional important information.
Please read Accenture's Recruiting and Hiring Statement for more information on how we process your data during the Recruiting and Hiring process.

Our client, a distinguished global pharmaceutical company, is actively recruiting for a dedicated and experienced Remote Clinical Research Associate (CRA) to join their cutting-edge research and development division. This fully remote position offers the flexibility to work from anywhere in the US, supporting pivotal clinical trials that advance groundbreaking medical treatments. As a remote CRA, you will be responsible for monitoring the progress of clinical trials at investigational sites, ensuring adherence to protocols, good clinical practice (GCP) guidelines, and all applicable regulatory requirements.

Your primary duties will include conducting pre-study, initiation, interim monitoring, and close-out visits from a remote capacity, utilizing advanced telecommunication and data management tools. You will review and verify source documentation, patient records, and case report forms (CRFs) for accuracy and completeness. Maintaining effective communication with investigators, site staff, and internal project teams is crucial for the successful execution of trials. The ideal candidate will be adept at identifying and resolving site issues, ensuring data integrity, and protecting patient safety. You will also be responsible for managing essential study documents and contributing to study start-up activities.

A Bachelor's degree in a life science, nursing, or related field is required. A minimum of 3-5 years of experience as a Clinical Research Associate is essential, with a proven track record of successful remote monitoring or a strong ability to transition to a remote-first role. Comprehensive knowledge of GCP, FDA regulations, and clinical trial processes is mandatory. Excellent organizational, time management, and interpersonal skills are critical for effective remote collaboration. Proficiency in electronic data capture (EDC) systems and other clinical trial management software is expected. This is an unparalleled opportunity to contribute to life-saving pharmaceutical innovations from the comfort of your own home.

Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is looking for an experienced Senior Clinical Research Associate to contribute to groundbreaking drug development in **St. Louis, Missouri, US**. This role is crucial for overseeing the execution of clinical trials, ensuring adherence to protocols, regulations, and good clinical practices. You will be instrumental in managing site relationships, monitoring trial progress, and ensuring data integrity throughout the study lifecycle. This is an exceptional opportunity to work with cutting-edge therapies and contribute to bringing life-saving treatments to patients.

Responsibilities will include selecting, training, and monitoring investigational sites; ensuring compliance with FDA regulations and ICH-GCP guidelines; conducting site visits (pre-study, initiation, monitoring, close-out); reviewing and verifying case report forms (CRFs) and source documents; resolving data discrepancies; managing trial supplies; and preparing study documentation. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, with a minimum of 5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry. A strong understanding of drug development processes, clinical trial design, and regulatory requirements is essential. Excellent organizational, problem-solving, and communication skills are a must. The ability to manage multiple projects simultaneously and a meticulous attention to detail are critical. Experience with various therapeutic areas and electronic data capture (EDC) systems is highly desirable. This position offers a competitive salary, comprehensive benefits package, and the chance to be part of a dynamic and collaborative research environment dedicated to advancing healthcare.

Our client, a leading pharmaceutical innovator, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dedicated clinical operations team. This role plays a critical part in ensuring the successful execution of clinical trials by overseeing study sites and ensuring compliance with protocols and regulations. While this position offers a hybrid work model, requiring some on-site presence, it provides a fantastic opportunity to contribute to life-changing therapies from St. Louis, Missouri, US .

Responsibilities:

• Conduct pre-study, initiation, interim, and close-out visits for clinical trial sites.
• Monitor study conduct to ensure adherence to the investigational plan, regulatory requirements, and Good Clinical Practice (GCP).
• Verify source data and documentation at clinical sites through source data verification (SDV).
• Manage communication between study sites, sponsors, and internal teams, addressing site issues promptly.
• Train site staff on study procedures, protocol requirements, and regulatory compliance.
• Ensure timely submission of study-related documents and adherence to data management timelines.
• Identify, document, and resolve site deviations and regulatory non-compliance issues.
• Manage site recruitment, enrollment, and retention strategies to meet study timelines.
• Contribute to the development and review of study protocols, case report forms (CRFs), and other study documents.
• Prepare site monitoring reports and provide regular updates on site progress and performance.
• Ensure accurate and timely entry of site visit reports into the clinical trial management system (CTMS).
• Build and maintain strong relationships with investigators, study coordinators, and other site personnel.

Qualifications:

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Minimum of 4-6 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role.
• Demonstrated knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
• Proven experience in site management, monitoring, and auditing clinical trial sites.
• Strong understanding of clinical trial processes and phases.
• Excellent interpersonal, communication, and negotiation skills.
• Ability to travel to sites as required (estimated 50-60% travel).
• Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• High attention to detail and excellent organizational skills.
• Ability to work independently and manage a diverse workload effectively.

This is an exciting opportunity to advance your career in clinical research and make a significant impact on global health.

Our client, a pioneering biopharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) specializing in Oncology to join their esteemed team in **St. Louis, Missouri, US**. This role is crucial for overseeing and managing clinical trials that evaluate novel cancer therapies, ensuring adherence to protocols, regulatory requirements, and ethical standards. The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out activities, acting as the primary liaison between the sponsor and clinical investigators. The ideal candidate will possess a strong understanding of oncology drug development, clinical trial methodologies, and regulatory landscapes (FDA, ICH-GCP).

Key Responsibilities:

• Conduct pre-study, site initiation, interim, and close-out visits to assess the quality and integrity of clinical trial conduct.
• Monitor clinical trial sites to ensure compliance with protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Verify the accuracy, completeness, and timeliness of source documentation and case report forms (CRFs).
• Manage study supplies and ensure proper storage and handling of investigational products.
• Identify, document, and resolve site-level issues and deviations.
• Serve as the primary point of contact for assigned clinical sites, fostering positive and productive working relationships with investigators and site staff.
• Train and mentor site personnel on study protocols, procedures, and regulatory requirements.
• Contribute to the development and review of clinical trial documents, including protocols, informed consent forms, and monitoring plans.
• Prepare and submit monitoring reports and track action items to resolution.
• Ensure timely data collection and query resolution to facilitate efficient database lock.

Qualifications:

• Bachelor's degree in a life science, nursing, or related scientific field. Advanced degree is a plus.
• Minimum of 5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical or biotechnology industry.
• Significant experience with oncology clinical trials is essential.
• Thorough knowledge of ICH-GCP guidelines, FDA regulations, and other relevant regulatory requirements.
• Proven ability to manage multiple clinical trial sites effectively.
• Excellent monitoring skills, including source data verification and review of regulatory documents.
• Strong written and verbal communication skills, with the ability to present information clearly and concisely.
• Exceptional organizational and time management skills, with meticulous attention to detail.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel up to 60% of the time, as required by the study.
• Must be legally authorized to work in the United States.

This hybrid role in **St. Louis, Missouri, US** offers a competitive salary, excellent benefits, and the opportunity to make a significant impact on the future of cancer treatment.

Our client, a leading global pharmaceutical company committed to advancing healthcare through innovative research and development, is seeking an experienced Senior Clinical Research Associate (CRA) to join their esteemed clinical operations team in St. Louis, Missouri, US . This hybrid role offers a blend of remote work flexibility and essential on-site responsibilities, providing an excellent balance for dedicated professionals. As a Senior CRA, you will be responsible for ensuring the effective monitoring and management of clinical trials across various therapeutic areas, adhering strictly to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. Your core duties will involve site selection, initiation, monitoring, and close-out visits to ensure data integrity, patient safety, and protocol compliance. You will build and maintain strong relationships with clinical investigators and site staff, providing them with the necessary support and guidance throughout the trial lifecycle. The Senior CRA will critically review and verify source documents against case report forms (CRFs), identify discrepancies, and ensure timely resolution. You will also be involved in the preparation and submission of essential study documents, and in tracking site performance metrics. This position demands a thorough understanding of clinical trial phases, drug development processes, and regulatory landscapes (FDA, EMA). The ideal candidate will possess exceptional organizational, communication, and problem-solving skills, with a meticulous attention to detail. This is a critical role that directly impacts the success of our client's drug development pipeline, contributing to bringing life-changing therapies to patients worldwide. The opportunity to work on diverse and impactful studies within a supportive and collaborative team environment in the vibrant biomedical research community of St. Louis makes this a highly rewarding career move.

Responsibilities:

• Conduct site selection, initiation, interim monitoring, and close-out visits for clinical trials.
• Ensure adherence to Good Clinical Practice (GCP) guidelines, ICH-GCP, and all applicable regulatory requirements.
• Verify accuracy and completeness of source documents against Case Report Forms (CRFs).
• Monitor patient safety, protocol compliance, and data integrity at assigned clinical sites.
• Build and maintain strong working relationships with investigators, site staff, and study teams.
• Identify, track, and resolve site-specific issues and discrepancies in a timely manner.
• Prepare and submit essential study documents, including monitoring reports and site correspondence.
• Ensure study supplies are adequate and properly managed at the investigational sites.
• Contribute to the development of study protocols and monitoring plans.
• Provide training and guidance to site personnel on study procedures and regulatory requirements.

Qualifications:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical industry.
• In-depth knowledge of GCP, ICH-GCP, FDA regulations, and clinical trial processes.
• Proven ability to conduct site visits and monitor clinical trials effectively.
• Excellent understanding of medical terminology and clinical trial documentation.
• Strong analytical, problem-solving, and critical thinking skills.
• Exceptional written and verbal communication skills.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to manage multiple studies and sites simultaneously.
• Valid driver's license and willingness to travel extensively.

Our client is a leader in scientific innovation, seeking a highly experienced and visionary Principal Research Scientist to join their fully remote R&D team. This pivotal role will drive groundbreaking research and development initiatives, pushing the boundaries of scientific knowledge and technological advancement. You will lead complex research projects, design and execute experiments, analyze data, and interpret results to contribute to novel discoveries and product development. The ideal candidate will possess a Ph.D. in a relevant scientific discipline (e.g., Physics, Chemistry, Biology, Engineering, Computer Science) and a strong publication record. Expertise in a specialized field relevant to our client's focus areas is essential. You will collaborate with a team of talented scientists and engineers, mentor junior researchers, and contribute to the strategic direction of our research pipeline. This position requires exceptional analytical, critical thinking, and problem-solving skills, along with the ability to communicate complex scientific concepts effectively to both technical and non-technical audiences. Experience with advanced research methodologies, experimental design, data analysis tools, and scientific modeling is crucial. We are looking for an innovative and self-motivated individual who can work independently in a remote setting, manage multiple research projects concurrently, and translate scientific insights into tangible technological applications. This role offers a unique opportunity to conduct cutting-edge research, make significant scientific contributions, and shape the future of innovation in a fully remote, collaborative environment.

Key Qualifications:

• Ph.D. in Physics, Chemistry, Biology, Engineering, Computer Science, or a related scientific field.
• 10+ years of post-doctoral research experience or equivalent in an industrial or academic setting.
• Demonstrated expertise in a specific scientific domain relevant to the company's R&D focus.
• Proven track record of leading research projects and publishing in peer-reviewed journals.
• Proficiency in experimental design, data analysis, and scientific modeling.
• Excellent written and verbal communication skills, with the ability to present complex scientific findings.
• Ability to work independently and manage research projects in a remote setting.
• Experience mentoring junior researchers is a plus.