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Clinical Project Associate Jobs in Missouri (NOW HIRING)

Jobgether

Ensure clinical projects within the assigned franchise are appropriately resourced and aligned with ... Research Associate or equivalent role, or 10+ years with equivalent education and training.

New

ClinChoice

Position Overview - Clinical Research Associate As a CRA, you'll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee ...

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Clinical Project Associate information

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$11

$29

$51

How much do clinical project associate jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical project associate 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 a Clinical Project Associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What is the difference between Clinical Project Associate vs Clinical Research Coordinator?

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Missouri? The most popular types of Clinical Project jobs in Missouri are:
What are popular job titles related to Clinical Project Associate jobs in Missouri? For Clinical Project Associate jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Clinical Project Associate jobs in Missouri look for? The top searched job categories for Clinical Project Associate jobs in Missouri are:
What cities in Missouri are hiring for Clinical Project Associate jobs? Cities in Missouri with the most Clinical Project Associate job openings:
Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Missouri as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $61,536 per year, or $29.6 per hour.

Senior Manager, Clinical Operations Site Management (Franchise Lead)

Jobgether

On-site, Remote

Full-time

Posted 3 days ago

New

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Manager, Clinical Operations Site Management (Franchise Lead) based in Netherlands.

Join a global clinical research organization dedicated to advancing healthcare innovation and improving patient outcomes through high-quality clinical trials. In this leadership role, you will provide strategic and operational expertise across clinical programs, ensuring successful delivery within a specialized therapeutic area. You will collaborate with cross-functional teams, support project execution strategies, and help drive operational excellence across complex clinical studies. The position offers the opportunity to influence clinical trial success, mentor teams, and contribute to meaningful scientific advancements. Working in a collaborative and inclusive environment, you will combine therapeutic expertise, leadership skills, and operational knowledge to make a measurable impact on global healthcare.

Accountabilities
  • Provide therapeutic and operational leadership throughout the clinical program and project delivery lifecycle, ensuring successful execution of assigned studies.
  • Partner with cross-functional teams to develop effective delivery strategies, resolve operational challenges, and optimize project outcomes.
  • Ensure clinical projects within the assigned franchise are appropriately resourced and aligned with operational goals.
  • Serve as a key point of contact for project management franchise leadership, supporting communication and strategic alignment.
  • Participate in proposal defense meetings and client discussions by providing clinical operations expertise and supporting business development activities.
  • Ensure clinical research teams are properly trained on study requirements, including protocols, standard operating procedures, quality processes, and clinical monitoring plans.
  • Collaborate with quality teams to identify training opportunities and support continuous improvement initiatives based on quality findings and corrective action plans.
  • Coordinate activities between project management, site management, and study start-up teams to ensure seamless study execution.
  • Establish and maintain regular operational reviews covering quality metrics, site performance, data quality, project health, resource allocation, and contractual deliverables.
  • Provide leadership and performance management support for direct reports, including conducting evaluations and supporting professional development.
Requirements
  • Bachelor's degree or equivalent higher education in biological sciences, physical sciences, health sciences, pharmacy, or a related discipline.
  • 8+ years of clinical research experience as a Clinical Research Associate or equivalent role, or 10+ years with equivalent education and training.
  • Minimum 2 years of people management or team leadership experience within clinical operations.
  • Strong knowledge of clinical trial delivery processes, drug development lifecycle, and the biopharmaceutical industry.
  • Experience managing or supporting CNS (Central Nervous System) clinical trials is required.
  • Broad understanding of clinical protocols, therapeutic areas, study operations, and global regulatory environments.
  • Strong strategic thinking, problem-solving abilities, and decision-making skills in complex operational settings.
  • Excellent planning, organizational, communication, and stakeholder management skills.
  • Ability to collaborate effectively with global, multidisciplinary teams and influence outcomes across functions.
  • Innovative mindset with the ability to identify opportunities for process improvement and operational excellence.
Benefits
  • Fully remote work opportunity.
  • Opportunity to contribute to impactful clinical research programs that improve patient outcomes.
  • Collaborative environment with experienced professionals across global therapeutic and operational teams.
  • Opportunity to influence clinical trial strategy and operational excellence at an international level.
  • Supportive workplace culture focused on inclusion, collaboration, and professional growth.
  • Access to opportunities for continuous learning and development within the clinical research field.
  • Ability to work alongside multidisciplinary experts across healthcare, science, and research domains.
  • Meaningful role with direct impact on advancing medical innovation and improving lives.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
 Why Apply Through Jobgether? 
 
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
 
 
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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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