CrawlJobs Logo
Advocate Health Care Logo Advocate Health Care · Research and Development

Senior Research Associate

United States, Charlotte 26.55 - 39.85 USD / Hour · Job Posted January 30, 2026
Apply Position
Job Link Share

Job Description

Join our mission to transform trauma care. As a Sr. Research Associate on our Trauma & Acute Care Surgery Research team, you’ll be at the forefront of groundbreaking studies that shape the future of critical care. Every day, your work will directly impact the care of critically ill and injured patients, helping advance treatments and improve outcomes for some of the most vulnerable populations. This is a fast-paced, high-impact position. Many of our studies require time-sensitive screening and enrollment, so adaptability and strong organizational skills are key. Our team provides 24/7/365 coverage at the Charlotte campus, ensuring research excellence around the clock.

Job Responsibility

  • Maintains designated applications in research department databases
  • Creates new databases, prepares and runs data analysis queries, and uploads local database to the national database center
  • Uses existing database to create reports as requested
  • Performs data manipulation and migration
  • Reviews data quality reports for data submissions and errors
  • Ensures data requests are received, have authorizations, are evaluated, and reported
  • Prepares specifications and summary reports for data queries and requests
  • Performs chart abstraction
  • Provides administrative support when needed

Requirements

  • Bachelor's Degree in Computer Science or health-related field required
  • Associates Degree and equivalent work experience will be considered
  • Training in information systems technologies, desktop application, and databases required
  • Experience with analytical software and database analysis and reports preferred
  • Prior experience in clinical trials, especially drug and/or device studies
  • Strong communication and teamwork skills
  • Ability to thrive in a fast-paced, high-acuity setting

What we offer

  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
Advocate Health Care - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Senior Research Associate

8 matching positions

Senior Research Associate

Seeking a QC Senior Research Associate with broad knowledge and expertise in ana...
Location
Location
United States , San Diego
Salary
Salary:
60.00 - 69.00 USD / Hour
bhsg.com Logo
Beacon Hill
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS or equivalent in relevant discipline with a minimum of 2-5 years of relevant industry experience or Master’s degree in relevant discipline with a minimum of 0-1 years of relevant industry experience
  • Experience in pharmaceutical industry with a GMP testing focus, ideally covering the analytical method and testing lifecycle from development through commercial drug product testing, with experience in a GMP QC release testing role
  • Experience in optimizing methods with particular emphasis on cell-based potency assay, molecular biology assay, and protein chemistry assays
  • Significant experience in an FDA-regulated environment
  • Entrepreneurial spirit, with strong willingness to take on new challenges required to bring novel medicines to the clinic
  • Excellent organizational and communication skills
Job Responsibility
Job Responsibility
  • Collaborate with research, analytical development and process development teams to develop, qualify/validate AAV gene therapy analytical/molecular biology assays, chemical/biochemical assays, and cell-based biological potency assays, for process monitoring and product release and stability, e.g., compendial methods, HPLC, DLS, droplet digital PCR or qPCR, ELISA, and cell‑based potency assays
  • Participate in developing timelines, protocols and reports for assay transfers, qualifications/validations Contribute to establishing material specifications for drug substance and drug products
  • Author and review QC analytical/equipment SOPs, protocols, and reports as needed
  • Ensure the timely execution of all routine QC testing, data review, and preparation of summary reports May act as an analytical lab representative on a CMC team
  • Perform quality management activities such as deviation, CAPA, change control, investigation of OOS, OOT and anomalous results within the company QMS according to established procedures.
  • Maintain QC laboratory, track critical reagents and equipment logbooks, and ensure all the equipment is calibrated
  • Utilize the LIMS system to submit samples, enter data, and track samples.
  • Utilize statistical analysis software to generate assay control charts and recommend assay acceptance criteria.
  • Learn and become proficient in all laboratory instrument software to conduct testing
Read More
Arrow Right

Senior Research Associate

Join Our Mission to Transform Trauma Care. Are you passionate about making a rea...
Location
Location
United States , Charlotte
Salary
Salary:
26.55 - 39.85 USD / Hour
advocatehealth.com Logo
Advocate Health Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree in Computer Science or health-related field required but Associates Degree and equivalent work experience will be considered
  • Training in information systems technologies, desktop application, and databases required
  • Experience with analytical software and database analysis and reports preferred
  • Prior experience in clinical trials, especially drug and/or device studies
  • Strong communication and teamwork skills
  • Ability to thrive in a fast-paced, high-acuity setting
Job Responsibility
Job Responsibility
  • Maintains designated applications in research department databases
  • Creates new databases, prepares and runs data analysis queries, and uploads local database to the national database center
  • Uses existing database to create reports as requested
  • Performs data manipulation and migration
  • Reviews data quality reports for data submissions and errors
  • Ensures data requests are received, have authorizations, are evaluated, and reported
  • Prepares specifications and summary reports for data queries and requests
  • Performs chart abstraction
  • Provides administrative support when needed
What we offer
What we offer
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Fulltime
Read More
Arrow Right

Senior Research Associate

Senior Research Associate is responsible for the completion of experiments and w...
Location
Location
United States , Portland
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 3+ years of laboratory bench experience, preferably in a regulated industry setting
  • PCR-based assay development and validation experience (Digital PCR experience preferred)
  • Strong proficiency in research methodologies and data analysis tools, with excellent attention to detail
  • Excellent analytical and problem-solving skills, with the ability to develop effective research strategies
  • Demonstrated ability to work collaboratively with cross-functional teams
  • Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment
  • Bachelors Degree in Life Sciences or a related field
Job Responsibility
Job Responsibility
  • Designing and implementing research studies to gather data and insights
  • Analyzing research data to identify trends, patterns, and areas for improvement
  • Collaborating with cross-functional teams to develop research methodologies and protocols
  • Preparing research reports and presentations to communicate findings to stakeholders
  • Ensuring data integrity and accuracy through rigorous validation processes
  • Staying updated on industry trends and emerging technologies to enhance research capabilities
  • Contributing to organizational growth through effective research and strategic planning
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Clinical Research Associate II / Senior Clinical Research Associate Large Pharma

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Germany , Frankfurt
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master or Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 2 years of experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
  • Excellent communication skills in German and English
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Job Responsibility
Job Responsibility
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Senior Clinical Research Associate or Clinical Research Associate II

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United States , Blue Bell
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 1-year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive)
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right
New

Senior Research Associate- Diagnostic Assay Development

10x Genomics is establishing a diagnostics effort, translating our leading singl...
Location
Location
United States , Pleasanton
Salary
Salary:
97700.00 - 132100.00 USD / Year
10xgenomics.com Logo
10x Genomics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. or M.S. in Molecular Biology, Genetics, Biochemistry, or a related scientific field
  • B.S. with 5+ years or M.S. with 3+ years of hands-on experience in molecular diagnostics or genomics assay development in an industry setting
  • Direct, demonstrable experience with advanced molecular technologies, particularly Next-Generation Sequencing (NGS) workflows
  • Exceptional proficiency in molecular biology techniques, including nucleic acid extraction, PCR/qPCR, and NGS library preparation
  • A proven track-record of using and optimizing and troubleshooting molecular biology protocols
  • Experience working with challenging clinical sample types (e.g., FFPE tissue, primary tumor cells, low-input samples)
  • Experience working within a quality system or environment governed by CLIA, CAP, or ISO 13485 standards strongly preferred
  • Prior hands-on experience with 10x Genomics single-cell or spatial technologies (e.g., Chromium or Xenium platforms) is a strong advantage
  • Experience with automated liquid handling for high-throughput assay execution is a strong advantage
  • experience with microscopy techniques a plus
Job Responsibility
Job Responsibility
  • Hands-on execution of complex single-cell and spatial genomics assays (e.g., sample processing, library preparation, sequencing)
  • Systematically troubleshoot, optimize, and refine specific steps within the assay workflow to improve performance, robustness, and efficiency
  • Perform feasibility studies on new reagents, instrumentation, and process improvements for clinical readiness
  • Prepare and process samples in support of large-scale clinical research studies
  • Generate and maintain meticulous laboratory records, protocols (SOPs), and batch records following Good Documentation Practices (GDP)
  • Execute formal experiments for analytical validation studies, including assessment of accuracy, precision, limit of detection, and reproducibility
  • Ensure all work is conducted under appropriate quality controls
  • Present experimental data clearly and concisely in team meetings and written reports
  • Support the transfer of robust assay workflows to the CLIA operations team
  • Collaborate closely with R&D Scientists, Automation Engineers, and Bioinformatics teams to meet project milestones
What we offer
What we offer
  • Equity grants
  • Comprehensive health and retirement benefit programs
  • Annual bonus program or sales incentive program
  • Health Package
  • Easy-to-use Benefits
  • Family oriented
  • Generous Time Off
  • Fulltime
Read More
Arrow Right

Senior Research Associate, Discovery Medicine

BigHat Biosciences is looking for a motivated and energetic Senior Research Asso...
Location
Location
United States , San Mateo
Salary
Salary:
100000.00 - 115000.00 USD / Year
BigHat Biosciences
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.Sc. degree in cell biology, molecular biology, biochemistry, genetics, immunology, or a related field, with at least 3 years of relevant experience, including 1 year in industry
  • Hands-on proficiency in standard immunology and cell biology techniques such as mammalian cell culture and multicolor flow cytometry
  • Previous experience with automation and high-throughput assays desired
  • Scientific curiosity and problem-solving abilities
  • A strong can-do mentality and desire to thrive in a dynamic start-up environment
  • The ability to communicate clearly and build open collaborative relationships.
Job Responsibility
Job Responsibility
  • Drive the development of therapeutics by owning the functional characterization of therapeutic candidates
  • Plan, execute, and analyze TDCC, T cell activation, cytokine release, FACS, ELISA, ADCC, and other relevant functional assays
  • Perform isolation and culture of primary immune cells from blood or tissue
  • Inform program plans based upon experimental results and make relevant recommendations for program conceptualization and advancement
  • Keep detailed and organized records of experimental protocols and results
  • Proactively and independently interpret and present scientific findings
  • Collaborate and communicate across a diverse research team to successfully progress scientific goals.
What we offer
What we offer
  • Range of health insurance plan options through Anthem and Kaiser (monthly credit if benefit waived)
  • Dental, and vision coverage through Guardian
  • Additional well-being benefits through Nayya, OneMedical, Wagmo, Rula, and more
  • 401(k) with company match
  • DTO, two weeks of company-wide shutdown, and 12 company holidays
  • Paid parental leave
  • bonus
  • options
  • Fulltime
Read More
Arrow Right

Senior Research Associate, CMC Quantitative Sciences

As a Data Engineer within Moderna’s CMC Quantitative Sciences (CMC QS) team, you...
Location
Location
United States , Norwood
Salary
Salary:
74000.00 - 118400.00 USD / Year
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS in a quantitative or scientific discipline (engineering, statistics, mathematics, computer science, data science, or related field) with 2 - 4+ years of relevant experience in data science/analytics in the pharmaceutical or biotechnology industry OR MS with 0 - 2+ years of relevant experience
  • Proficiency with statistical software and methods, including DOE, multivariate analysis, regression, and statistical process control (e.g., JMP, Minitab, R, SAS, Python)
  • Hands-on experience with programming languages (R, Python, SQL) to manipulate, analyze, and visualize complex datasets
  • Familiarity with business analytics/visualization tools (e.g., Tableau, Power BI, Spotfire)
  • This position is site-based, requiring you to be at Moderna’s site full-time
Job Responsibility
Job Responsibility
  • Partnering with Manufacturing, Technical Development, and Quality functions to deliver data-driven analyses, dashboards, and digital solutions that support operations and continuous improvement
  • Leading the development and maintenance of data engineering pipelines, contextualization systems, and data intake workflows that enable seamless and validated information flow
  • Creating and deploying advanced analytical tools such as statistical process control, multivariate analyses, and automated reporting systems to support technical investigations and performance monitoring
  • Supporting investigations and root cause analyses by performing deep data manipulation and applying sound statistical techniques with clear communication of outcomes
  • Collaborating with cross-functional teams to implement digital tools and analytics platforms by contributing to technical requirements, validation, and solution optimization processes
  • Advocating for and modeling strong statistical and analytics practices to drive consistency across CMC QS and broader partner teams
  • Troubleshooting data pipeline and analytics reliability issues and identifying opportunities to streamline or automate workflows
  • Providing informal guidance and technical mentorship to partners and junior staff on data best practices
  • Engaging with opportunities to integrate and explore generative AI tools as part of the evolving digital manufacturing toolkit
  • Contributing to Moderna’s commitment to digital innovation in biomanufacturing through additional tasks as assigned
What we offer
What we offer
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras
  • Fulltime
Read More
Arrow Right