IQVIA
GlobalSiteActivationIdentificationSpecialist-freelancer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Global Site Activation Identification Specialist - freelancer at IQVIA. Skills: Site identification, Feasibility, Clinical trials. Conduct global site identification and feasibility activities. Analyze data sources and study requirements”
What They're Looking For.
Must Have
Degree in Life Sciences or related clinical background, Prior experience in clinical research, understanding of clinical trial processes and site feasibility, Proven ability to read and interpret clinical trial protocols, data analysis skills, Excellent English language skills
Nice to Have
Experience in site identification, feasibility, or site activation, Familiarity with CDA and feasibility questionnaire processes, any additional European language a plus
What You'll Do.
Conduct global site identification and feasibility activities
Analyze data sources and study requirements
Identify and prioritize suitable investigator sites
Review clinical trial protocols
Translate study requirements into clear site profiles
Perform site vetting and qualification assessments
Lead and manage site outreach activities
Support development and distribution of feasibility questionnaires
Manage CDA collection
Track feasibility responses
Maintain accurate documentation
and professional communication
How You'll Work.
Team & Collaboration
Global study teams; Internal teams; External sites; Start-up teams; Local stakeholders
Communication Scope
Written communication; Verbal communication
Full Job Description
# **Global Site Identification Specialist (Freelance)** **Location:** Europe (Home-based) **FTE:** 0.5 – 1.0 **Contract Type:** Freelance / Contractor ## ## **About the Role** We are seeking an experienced **Global Site Identification Specialist** to support clinical trials through targeted site identification and feasibility activities. This role plays a critical part in ensuring the selection of high-performing investigative sites aligned with study requirements. Working closely with global study teams, you will combine clinical expertise, data analysis, and operational insight to identify, evaluate, and engage potential sites across Europe. ## ## **Key Responsibilities** * Conduct global site identification and feasibility activities to support clinical trial start-up * Analyze data sources and study requirements to identify and prioritize suitable investigator sites * Review clinical trial protocols and translate study requirements into clear site profiles * Perform site vetting and qualification assessments based on feasibility criteria and site capabilities * Lead and manage site outreach activities, including initial engagement and follow-up * Support the development and distribution of feasibility questionnaires (FQ) * Manage CDA collection, tracking, and follow-up to ensure timely execution * Track feasibility responses and maintain accurate documentation * Collaborate cross-functionally with study teams, start-up, and local stakeholders * Ensure clear, timely, and professional communication with internal teams and external sites ## ## **Qualifications & Experience** * Degree in Life Sciences or related clinical background * Prior experience in clinical research, ideally as a Clinical Research Associate (CRA) or similar role * Strong understanding of clinical trial processes and site feasibility * Proven ability to read and interpret clinical trial protocols * Experience in site identification, feasibility, or site activation is highly preferred * Familiari
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