Serving as the primary FSA contact for internal teams and customers for study-level start-up matters. * Contributing to process improvement and best practice sharing within the FSA project management ...
Posted today
Quick apply
Serving as the primary FSA contact for internal teams and customers for study-level start-up matters. * Contributing to process improvement and best practice sharing within the FSA project management ...
Posted today
Quick apply
Serving as the primary FSA contact for internal teams and customers for study-level start-up matters. * Contributing to process improvement and best practice sharing within the FSA project management ...
Posted today
Salt Lake City, UT · On-site
$165.90 - $211.10/hr
... start-up to study closure with support or direction from an Associate Director/Director of Clinical Operations. In this role, you will: * Lead all aspects of clinical trial execution for one or more ...
Salt Lake City, UT · On-site
$165.90 - $211.10/hr
... start-up to study closure with support or direction from an Associate Director/Director of Clinical Operations. In this role, you will: * Lead all aspects of clinical trial execution for one or more ...
Salt Lake City, UT · On-site
$71K - $189K/yr
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...
Salt Lake City, UT · On-site
$71K - $189K/yr
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...
Salt Lake City, UT · On-site
$71K - $189K/yr
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...
Salt Lake City, UT · On-site
$71K - $189K/yr
Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... May participate in study start-up activities, site budget tracking, financial management, and site ...
Prepare clinical sites for study start-up by conducting site initiation visits. * Analyze and ... Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified ...
Prepare clinical sites for study start-up by conducting site initiation visits. * Analyze and ... Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified ...
Salt Lake City, UT · On-site
$47K - $90K/yr
Prepare clinical sites for study start-up by conducting site initiation visits. * Analyze and ... Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified ...
Salt Lake City, UT · On-site
$47K - $90K/yr
Prepare clinical sites for study start-up by conducting site initiation visits. * Analyze and ... Preferences include credentialing as a Certified Clinical Research Associate (CCRA), Certified ...
Salt Lake City, UT · Hybrid
$39K - $85K/yr
... study start-up by reviewing and tracking regulatory documents, ordering start-up supplies and ... associates. 13. Perform other duties as assigned by management. Problem Solving This position ...
Salt Lake City, UT · Hybrid
$39K - $85K/yr
... study start-up by reviewing and tracking regulatory documents, ordering start-up supplies and ... associates. 13. Perform other duties as assigned by management. Problem Solving This position ...
Salt Lake City, UT · On-site
$39K - $85K/yr
... study start-up by reviewing and tracking regulatory documents, ordering start-up supplies and ... associates. 13. Perform other duties as assigned by management. Problem Solving This position ...
Salt Lake City, UT · On-site
$39K - $85K/yr
... study start-up by reviewing and tracking regulatory documents, ordering start-up supplies and ... associates. 13. Perform other duties as assigned by management. Problem Solving This position ...
Salt Lake City, UT · On-site
$60K - $78K/yr
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
Salt Lake City, UT · On-site
$60K - $78K/yr
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
Salt Lake City, UT · On-site
$74K/yr
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
Salt Lake City, UT · On-site
$74K/yr
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
... study start up and oversee workload resourcing for team while providing primary point of contact support for completion of start-up activities (i.e., initiating CDA, Feasibility, MDG scoring and ...
Salt Lake City, UT · On-site +1
You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up ...
New
Salt Lake City, UT · On-site +1
You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up ...
New
Salt Lake City, UT · On-site
$25K/mo
The Regulatory Affairs Specialist will collaborate with study teams, institutional review boards (IRB), and external sponsors to support study start-up, maintenance, and closeout activities. The role ...
Salt Lake City, UT · On-site
$25K/mo
The Regulatory Affairs Specialist will collaborate with study teams, institutional review boards (IRB), and external sponsors to support study start-up, maintenance, and closeout activities. The role ...
Salt Lake City, UT · On-site
$120 - $180/hr
... of modern data sources and study designs, and expand the Division's methodological and ... The University of Utah offers highly competitive salaries and start-up packages and exceptional ...
Salt Lake City, UT · On-site
$120 - $180/hr
... of modern data sources and study designs, and expand the Division's methodological and ... The University of Utah offers highly competitive salaries and start-up packages and exceptional ...
Washington, UT · On-site
$16/hr
A Retail Stocking Associate (part-time) is a valued member of a high performing team who is ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Washington, UT · On-site
$16/hr
A Retail Stocking Associate (part-time) is a valued member of a high performing team who is ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Lehi, UT · On-site
$16/hr
A Retail Stocking Associate (part-time) is a valued member of a high performing team who is ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Lehi, UT · On-site
$16/hr
A Retail Stocking Associate (part-time) is a valued member of a high performing team who is ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Price, UT · On-site
$14.50/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Price, UT · On-site
$14.50/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Salt Lake City, UT · On-site
$16/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Salt Lake City, UT · On-site
$16/hr
A Retail Sales Associate (part-time) is a valued member of a high performing team who is empowered ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Cedar City, UT · On-site
$14.75/hr
A Retail Stocking Associate (part-time) is a valued member of a high performing team who is ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
Cedar City, UT · On-site
$14.75/hr
A Retail Stocking Associate (part-time) is a valued member of a high performing team who is ... start-up. We have over 1,600 stores in 48 states across the country and are opening several new ...
$11.60 - $15.12
3% of jobs
$15.12 - $18.64
18% of jobs
$19.34 is the 25th percentile. Wages below this are outliers.
$18.64 - $22.16
20% of jobs
The median wage is $24.30 / hr.
$22.16 - $25.68
15% of jobs
$25.68 - $29.21
11% of jobs
$29.21 - $32.73
4% of jobs
$35.72 is the 75th percentile. Wages above this are outliers.
$32.73 - $36.25
5% of jobs
$36.25 - $39.77
8% of jobs
$39.77 - $43.29
6% of jobs
$43.29 - $46.81
6% of jobs
$46.81 - $50.33
3% of jobs
$11
$28
$50
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
For Study Start Up Associate jobs in Utah, the most frequently searched job titles are:
The top searched job categories for Study Start Up Associate jobs in Utah are:
Cities in Utah with the most Study Start Up Associate job openings:

Salt Lake City, UT • On-site
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 14 hours ago
Posted today
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Title: Project Manager, FSA
Role Summary:
As a Project Manager, Feasibility and Site Activation (FSA) at ICON, you will be responsible for planning and manage Feasibility and Site Activation (FSA) activities for assigned clinical studies.
What You Will Do:
You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
Developing and managing FSA project plans, timelines, and deliverables for assigned studies.
Coordinating feasibility assessments, country and site recommendations, and start-up strategies in collaboration with functional experts.
Overseeing essential document collection, ethics and regulatory submissions, and site activation milestones.
Tracking progress against timelines and KPIs, proactively identifying risks and implementing mitigation plans.
Serving as the primary FSA contact for internal teams and customers for study-level start-up matters.
Contributing to process improvement and best practice sharing within the FSA project management team.
Your Profile:
You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent experience.
Strong experience in clinical research with a focus on feasibility, site activation, or start-up project management.
Proven ability to manage project plans, timelines, and cross-functional coordination in a fast-paced environment.
Good understanding of regulatory, ethics, and contractual requirements affecting study start-up.
Excellent communication, organizational, and stakeholder management skills.
Detail-oriented and proactive, with a commitment to quality, predictability, and customer satisfaction.
Willingness to travel as required (approximately 10%)
Title: Senior Project Manager, FSA
Role Summary:
Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality output, and exceeding sponsor expectations. Accountable for the overall coordination, implementation and completion of site activation activities for large global or complex projects of work in line with ICON/sponsor SOPs as appropriate, including regulatory/ethics, site contracts, essential documents, and site activations. Interacts with internal teams and stakeholders, as well as sponsor teams and stakeholders, and presents to Exec Management as needed.
Responsibilities:
Recognize, exemplify and adhere to ICON's values , and contribute to the “Own It” culture at ICON
Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted resources, with quality output, and exceeding sponsor expectations.
Accountable for the overall coordination, implementation and completion of site activation activities for large global or complex projects of work in line with ICON/sponsor SOPs as appropriate, including regulatory/ethics, site contracts, essential documents, and site activations.
Interacts with internal teams and stakeholders, as well as sponsor teams and stakeholders, and presents to Exec Management as needed.
Lead studies with highest quality standards to exceed customer expectations.
Review study and partnership budgets for proposals and sales as needed.
Drive assigned studies to meet KPIs and delight customers and sites
Act as customer point of contact for assigned studies; resolve study issues and drive exceptional customer delivery
Represent FSA at audits and inspections
Participate in Business Development opportunities to support the growth of the assigned portfolio, function, and/or region/country(ies)
Travel (approximately 10% depending on country structure and direct report levels) domestic and/or international
Responsible for performing activities that are in compliance with applicable corporate and departmental policies, standard operating procedures and operating guidelines and performing other duties as assigned by the management
Act as a mentor where required
What you need:
Bachelor's Degree
3-6 years of experience in a Clinical Research environment
Demonstrate proficient organizational skills and ability to prioritize tasks with minimal management support and oversight.
Exhibits extensive competency in Microsoft Office Suite applications (i.e. Word, Excel, Powerpoint, Outlook).
Completes tasks independently on time and in an efficient manner.
Ability to mentor and train others as needed.
Show confidence in dealing with internal stakeholders.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply