ZipRecruiter

Log In

1

Site Activation Study Jobs (NOW HIRING)

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 Holdings

Sr Site Activation Coordinator

You will perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions, working ...

Pfizer

Site Activation Partner (Sr. Associate)

Site Activation Partner The Site Activation Partner is responsible for leading and supporting operational activities from start-up to close-out, for assigned studies and investigator sites ensuring ...

Syneos Health Inc

Site Activation Specialist I

Site Activation Specialist I Syneos Health ® is a leading fully-integrated life sciences services ... studies based on the requirements of the clinical trial. * May be asked to perform: Local ...

Systimmune

Sr. Study Startup Specialist

Princeton, NJ · On-site

$90K - $115K/yr

The Senior Specialist drives timely site activation and enrollment readiness in compliance with ICH-GCP, SOPs, and local regulatory requirements, while identifying and mitigating risks, optimizing ...

next page

Showing results 1-20

All JobsSite Activation Study Jobs

Site Activation Study information

See salary details

$9

$17

$23

How much do site activation study jobs pay per hour?

As of Jul 7, 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 are Site Activation Study professionals and what do they do?

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 some common challenges faced by professionals 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 are the key skills and qualifications needed to thrive in Site Activation Study roles, and why are they important?

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 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.

More about Site Activation Study jobs
What cities are hiring for Site Activation Study jobs? Cities with the most Site Activation Study job openings:
What states have the most Site Activation Study jobs? States with the most job openings for Site Activation Study jobs include:
What job categories do people searching Site Activation Study jobs look for? The top searched job categories for Site Activation Study jobs are:
Site Activation Study jobs near you
Infographic showing various Site Activation Study job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, 12% Part Time, 1% Temporary, 3% Contract, and 1% Summer. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $37,203 per year, or $17.9 per hour.
Site Activation Specialist - Germany

Site Activation Specialist - Germany

IQVIA Holdings

Remote

Other

Posted 4 days ago

Job description

Freelance Site Activation Specialist – Germany (Home-Based)

Location: Germany (home-based) Contract type: Freelance

FTE: 1.0 - full time Start: immediately Duration: around 4 month

About the Role

We are looking for a Freelance Site Activation Specialist based in Germany to support country-level clinical trial start-up and site management activities.

This role focuses on feasibility, site identification, regulatory submissions, and activation, with some involvement in maintenance activities. Candidates with experience in Switzerland or exposure to the DACH region are highly preferred.

Key Responsibilities
  • Act as the primary point of contact for assigned investigative sites
  • Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines
  • Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy
  • Support contract and budget processes in collaboration with internal stakeholders
  • Maintain and update tracking tools, timelines, and internal systems with accurate project data
  • Monitor and report on site activation progress and performance metrics
  • Ensure compliance with ICH-GCP, local regulations (Germany and ideally Switzerland), and study requirements
  • Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams
Requirements
  • Based in Germany with strong understanding of the local regulatory environment
  • 2–3+ years of experience in site activation, study start-up, or clinical research
  • Bachelor's degree in Life Sciences or related field
  • Solid knowledge of clinical trial start-up processes and regulatory requirements
  • Experience managing site documentation and submission processes
  • Strong attention to detail and ability to manage multiple sites and timelines
  • Fluent in German and English (written and spoken)
  • Experience working on clinical studies in Switzerland or familiarity with Swiss regulatory requirements an advantage
  • Exposure to cross-border (DACH) studies an advantage

If this role sounds of interest, please apply today!

Apply