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Site Activation Study Jobs in Oregon (NOW HIRING)

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 ...

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 ...

Marketing Manager

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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 ...

... 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 ...

Site Activation Study information

See Oregon salary details

$9

$18

$24

How much do site activation study jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for site activation study in Oregon is $18.91, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $20.34 per hour, depending on experience, location, and employer.

What is a site activation study?

Site Activation Study professionals are responsible for overseeing and managing the process of initiating clinical trial sites. Their main tasks include coordinating regulatory document collection, ensuring sites comply with study protocols, and facilitating the start-up activities necessary for clinical trials. They work closely with investigators, site staff, and sponsors to guarantee that all requirements are met for a trial to begin at each site. Their role is crucial for ensuring timely and efficient study launches while maintaining regulatory compliance.

What are the key skills and qualifications needed for site activation study roles?

To thrive in a Site Activation Study role, you need a solid understanding of clinical research processes, regulatory requirements, and project management, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory submission platforms, and Good Clinical Practice (GCP) certification is often required. Strong attention to detail, excellent organizational skills, and effective communication abilities are vital for coordinating with multiple stakeholders and ensuring timely site activation. These skills and qualifications are essential to efficiently navigate complex regulatory environments and to ensure clinical trials start on schedule.

What are common challenges faced in site activation study roles, and how can they be overcome?

Professionals in Site Activation Study roles often encounter challenges such as tight timelines for site initiation, navigating varying regulatory requirements across regions, and coordinating with multiple stakeholders. Successfully overcoming these challenges requires strong organizational skills, clear communication, and a proactive approach to problem-solving. Building collaborative relationships with clinical sites and staying updated on regulatory changes can also help streamline activation processes and minimize delays.

What is the difference between Site Activation Study vs Site Coordinator?

AspectSite Activation StudySite Coordinator
Primary RolePlanning and overseeing the setup of clinical trial sitesManaging daily site operations and participant coordination
Required CredentialsClinical research experience, sometimes certificationsExperience in clinical settings, organizational skills
Work EnvironmentResearch sites, clinical trial settingsClinical sites, hospitals, research facilities
Industry UsageUsed during trial startup phaseOngoing 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.

What are popular job titles related to Site Activation Study jobs in Oregon?

For Site Activation Study jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Site Activation Study jobs?

Cities in Oregon with the most Site Activation Study job openings:

(Sr) Project Manager, Feasibility Site Activation

Portland, OR โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

New


Job description

(Sr) Project Manager, Feasibility Site Activation

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:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

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