Developing and managing FSA project plans, timelines, and deliverables for assigned studies ... You will have solid site start-up and activation experience, with the ability to manage competing ...
New
Quick apply
Developing and managing FSA project plans, timelines, and deliverables for assigned studies ... You will have solid site start-up and activation experience, with the ability to manage competing ...
New
Quick apply
Developing and managing FSA project plans, timelines, and deliverables for assigned studies ... You will have solid site start-up and activation experience, with the ability to manage competing ...
New
Dallas, OR ยท On-site
$80 - $110/hr
... regulatory activation, staffing, technology implementation, and study launch. Working cross functionally you\'ll ensure each site is delivered on time, on budget, and fully prepared to enroll ...
Dallas, OR ยท On-site
$80 - $110/hr
... regulatory activation, staffing, technology implementation, and study launch. Working cross functionally you\'ll ensure each site is delivered on time, on budget, and fully prepared to enroll ...
OR ยท On-site +1
Provide enrollment support and ensure progress by responding to site activation and * recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment ...
OR ยท On-site +1
Provide enrollment support and ensure progress by responding to site activation and * recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment ...
OR ยท On-site +1
Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation ...
OR ยท On-site +1
Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation ...
OR ยท On-site +1
Global Study Execution & Enrollment Enablement: Collaborate with Clinical Operations and regional teams to anticipate recruitment risks (including competing trials), support site activation strategy ...
OR ยท On-site +1
Global Study Execution & Enrollment Enablement: Collaborate with Clinical Operations and regional teams to anticipate recruitment risks (including competing trials), support site activation strategy ...
OR ยท On-site +1
... study operational issues; and participates in process improvement initiatives. To Make an Impact, You Will: * Lead feasibility assessments, site selection, and activation for cardiology centers ...
OR ยท On-site +1
... study operational issues; and participates in process improvement initiatives. To Make an Impact, You Will: * Lead feasibility assessments, site selection, and activation for cardiology centers ...
OR ยท On-site +1
Media plans will be aligned to business priorities, study recruitment needs, geographic opportunity ... Channel Activation & Expansion * Set the strategy for existing and emerging paid media channels ...
OR ยท On-site +1
Media plans will be aligned to business priorities, study recruitment needs, geographic opportunity ... Channel Activation & Expansion * Set the strategy for existing and emerging paid media channels ...
OR ยท On-site +1
You will plan and deliver Liftoff's conference presence, owned events, and regional activations ... studies, and event-related content that positions Liftoff as an industry leader. * Work cross ...
OR ยท On-site +1
You will plan and deliver Liftoff's conference presence, owned events, and regional activations ... studies, and event-related content that positions Liftoff as an industry leader. * Work cross ...
OR ยท On-site +1
... site search intent dataset outside of walled gardens, direct SDK integrations with top apps ... You will own the visual layout of sales decks, case studies and more. Beyond active deal support ...
OR ยท On-site +1
... site search intent dataset outside of walled gardens, direct SDK integrations with top apps ... You will own the visual layout of sales decks, case studies and more. Beyond active deal support ...
$9.91 - $11.23
2% of jobs
$11.23 - $12.55
1% of jobs
$12.55 - $13.86
0% of jobs
$13.86 - $15.18
5% of jobs
$15.18 - $16.50
8% of jobs
$17.06 is the 25th percentile. Wages below this are outliers.
$16.50 - $17.81
19% of jobs
The median wage is $18.55 / hr.
$17.81 - $19.13
25% of jobs
$20.38 is the 75th percentile. Wages above this are outliers.
$19.13 - $20.45
15% of jobs
$20.45 - $21.76
7% of jobs
$21.76 - $23.08
8% of jobs
$23.08 - $24.40
8% of jobs
$9
$18
$24
| Aspect | Site Activation Study | Site Coordinator |
|---|---|---|
| Primary Role | Planning and overseeing the setup of clinical trial sites | Managing daily site operations and participant coordination |
| Required Credentials | Clinical research experience, sometimes certifications | Experience in clinical settings, organizational skills |
| Work Environment | Research sites, clinical trial settings | Clinical sites, hospitals, research facilities |
| Industry Usage | Used during trial startup phase | Ongoing site management during trials |
While both roles are involved in clinical trials, the Site Activation Study focuses on preparing and initiating trial sites, whereas the Site Coordinator manages daily operations once the site is active. Understanding these differences helps in selecting the right role for your career or hiring needs.
For Site Activation Study jobs in Oregon, the most frequently searched job titles are:
The top searched job categories for Site Activation Study jobs in Oregon are:
Cities in Oregon with the most Site Activation Study job openings:
Portland, OR โข On-site
Full-time
Medical, Dental, Vision, Life, Retirement
Posted yesterday
New
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