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Site Activation Study Jobs (NOW HIRING)

worldwide.com

Site Activation Manager

Durham, NC · On-site

Serve as the primary point of accountability for site activation and start‐up activities on assigned studies.* Oversee cross‐functional site activation activities to ensure milestones are ...

IQVIA, Inc.

Site Activation Manager

Durham, NC · On-site

... studies as determined by Company, scope of work and/or sponsor requirements. Essential Functions • Provides strategic planning and project oversight accelerating Site Activation through best in ...

IQVIA

Site Activation Manager

Durham, NC · On-site

Study Delivery Scope minimum expectations: accountable for multiple regions or Global SAM project oversight responsibilities. Develop, implement and maintain the Site Activation Management Plan ...

IQVIA

Site Activation Manager

Durham, NC · On-site

Study Delivery Scope minimum expectations: accountable for multiple regions or Global SAM project oversight responsibilities. Develop, implement and maintain the Site Activation Management Plan ...

ICON

Site Activation Lead

Site Activation Lead ICON is a global healthcare intelligence and clinical research organisation ... Partner with Clinical Operations teams, and TAU partners to improve overall study start up metrics ...

ICON Clinical Research

Site Activation Lead

Site Activation Lead ICON plc is a world-leading healthcare intelligence and clinical research ... Partner with Clinical Operations teams, and TAU partners to improve overall study start up metrics ...

CTI

Study Activation Manager

Raleigh, NC · On-site

Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone ...

CTI

Study Activation Manager

Raleigh, NC · On-site

Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone ...

IQVIA

Site Activation Specialist

Durham, NC · On-site

$49K - $123K/yr

Essential Functions With moderate oversight and supervision, werve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for ...

New

Worldwide

What the Senior Site Activation Manager does at Worldwide This is a seasoned leadership role ... Serve as the primary point of communication and accountability for study start-up and maintenance ...

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Site Activation Study information

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How much do site activation study jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for site activation study in the United States is $17.89, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $19.23 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.

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What states have the most Site Activation Study jobs?

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

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Site Activation Study jobs near you
Infographic showing various Site Activation Study job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 2% As Needed, 81% Full Time, 13% Part Time, and 3% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $37,203 per year, or $17.9 per hour.

Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) - UK Remote

Remote

MCRA, LLC
Medical Equipment and Supplies Manufacturing • 51 - 200 employees
Learn more about MCRA, LLCexternal

Other

Posted 6 days ago

Job description

Job Title: Freelance Site Activation Specialist

We are seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities.

The primary focus of this role will be UK submission document collection and preparation, site document review, Informed Consent Form (ICF) adaptations, and regulatory submission support. The successful candidate will work closely with investigative sites and internal study teams to ensure submission packages are complete, compliant, and delivered according to project timelines.

Key Responsibilities
  • Collect, review, and prepare site and regulatory documentation required for UK clinical trial submissions
  • Support the preparation and submission of regulatory packages in accordance with study requirements and local regulations
  • Perform and coordinate Informed Consent Form (ICF) adaptations and associated document updates
  • Review essential site documentation to support Regulatory Green Light readiness
  • Liaise directly with investigative sites to obtain, track, and resolve outstanding documentation
  • Ensure the completeness, accuracy, and quality of submission packages
  • Maintain study tracking systems, timelines, and submission records
  • Support site activation activities and monitor progress against project milestones
  • Collaborate closely with Site Activation Managers, Regulatory Affairs, Project Management, and other cross-functional teams
  • Ensure compliance with ICH-GCP, local UK regulations, and study-specific requirements
Requirements
  • Based in the United Kingdom
  • Minimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical Research
  • Strong experience with site document collection, review, and submission preparation
  • Experience supporting clinical trial regulatory submissions in the UK
  • Experience performing ICF adaptations
  • Solid understanding of site activation and study start-up processes
  • Strong attention to detail and ability to manage multiple priorities and timelines
  • Bachelor's degree in Life Sciences or a related field
  • Fluent English communication skills, both written and verbal

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