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Associate Clinical Study Manager Jobs in Missouri

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Associate Clinical Study Manager information

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How much do associate clinical study manager jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for associate clinical study manager in Missouri is $29.58, according to ZipRecruiter salary data. Most workers in this role earn between $19.86 and $38.99 per hour, depending on experience, location, and employer.

What is an associate clinical study manager?

Associate Clinical Study Managers are professionals who support the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They work closely with Clinical Study Managers and other team members to ensure studies are conducted in compliance with regulatory guidelines and timelines. Their responsibilities often include overseeing documentation, coordinating with study sites, tracking study progress, and assisting with data management. This role is essential for ensuring that clinical studies run smoothly and efficiently, contributing to the development of new treatments and therapies.

What are the key skills and qualifications needed to thrive as an associate clinical study manager?

To thrive as an Associate Clinical Study Manager, you need a solid understanding of clinical trial processes, regulatory guidelines, and project management principles, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating study activities and collaborating with cross-functional teams. These skills ensure clinical studies are conducted efficiently, compliantly, and with high data integrity.

What are the main challenges an associate clinical study manager faces when coordinating multiple clinical trials simultaneously?

As an Associate Clinical Study Manager, balancing multiple trials often involves managing tight timelines, ensuring regulatory compliance, and coordinating with cross-functional teams such as data management, regulatory affairs, and site staff. Juggling these responsibilities can be challenging, especially when unexpected issues arise at different study sites or timelines shift. Strong organizational skills, proactive communication, and adaptability are key to effectively managing these complexities and keeping studies on track.

What is the difference between Associate Clinical Study Manager vs Clinical Study Coordinator?

AspectAssociate Clinical Study ManagerClinical Study Coordinator
ResponsibilitiesOversees study operations, manages teams, ensures compliance, and supports study planningCoordinates daily study activities, manages participant scheduling, and assists with data collection
Required CredentialsBachelor’s degree in life sciences, clinical research experience, often some project management knowledgeBachelor’s degree, clinical research or healthcare background, strong organizational skills
Work EnvironmentTypically in clinical research teams within pharmaceutical or biotech companiesOften in clinical sites or research facilities, supporting study execution
Industry UsageCommonly in pharmaceutical, biotech, and CRO settingsPrimarily in clinical research sites and hospitals

The Associate Clinical Study Manager and Clinical Study Coordinator roles share similarities in supporting clinical trials, but the manager has broader oversight and leadership responsibilities. The coordinator focuses on daily operational tasks, while the manager oversees study progress and compliance.

What cities in Missouri are hiring for Associate Clinical Study Manager jobs?

Cities in Missouri with the most Associate Clinical Study Manager job openings:

Associate Clinical Study Manager jobs near you

Senior Study Manager, Immunology

California, MO • On-site

Jobtailor
See more jobs at Jobtailorexternal

Other

Posted 2 days ago

New

Job description

  • Lead operational planning, feasibility, and execution of one or more clinical trials or significant aspects of trials in the Tulisokibart immunology program
  • Serve as clinical trial team lead when needed
  • Lead study planning, development, and execution elements, including data management deliverables, trial plans and timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, status reports, and study closeout
  • Lead timeline management, risk identification and mitigation, and issue resolution
  • Facilitate collaboration with internal and external stakeholders, including study teams, country teams, vendors, and committees
  • Manage study-specific partners and vendors
  • Represent the company through external partnerships, collaborations, and strategic engagements
  • Lead meetings and influence peers in a matrix environment
  • Drive operational milestones and study goals
Requirements
  • Bachelor's Degree and 5+ years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR Master's Degree and 3+ years of such experience OR PhD/PharmD Degree
  • Degree in life sciences preferred
  • Experience conducting global clinical trials, including trial initiation through database lock
  • Highly preferred: experience conducting clinical trials for Gastroenterology, Dermatology, or Rheumatology, especially autoimmune or immune-mediated disorders
  • Experience managing and driving operational activities on protocols for immunology-related clinical trials
  • Solid knowledge of clinical research regulatory requirements, including GCP and ICH
  • Ability to manage multiple competing priorities
  • Understanding of project planning and project management principles
  • Analytical, problem-solving, prioritization, conflict-resolution, and critical-thinking skills
  • Strong communication, writing, and presentation skills
  • Intermediate knowledge of Microsoft Office or similar, including Excel, PowerPoint, Word, and Outlook
  • No visa sponsorship
  • 10% travel
  • Valid driving license not required
Core Competencies

Demonstrates expertise in leading clinical trial operations, including planning, execution, and compliance with regulatory requirements. Proficient in managing cross-functional teams and driving project milestones in the immunology domain.

Highest-signal resume keywords
  • Clinical Trial Management
  • Project Management
  • Regulatory Compliance (GCP, ICH)
  • Immunology Clinical Trials
  • Stakeholder Collaboration
ATS Optimization KeywordsHard Skills
  • Clinical Drug Development
  • Data Management
  • Trial Planning
  • Risk Identification and Mitigation
  • Operational Activities Management
  • Analytical Skills
  • Problem-Solving Skills
  • Project Planning Principles
Soft Skills
  • Strong Communication Skills
  • Conflict Resolution
  • Critical Thinking
  • Prioritization Skills
Industry Keywords
  • Clinical Trials
  • Gastroenterology
  • Dermatology
  • Rheumatology
  • Autoimmune Disorders
  • Life Sciences
Tools & Technologies
  • Microsoft Office
  • Excel
  • PowerPoint
  • Word
  • Outlook
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