Site Feasibility Specialist - Freelance

7 LOCATIONS (OTHER)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

Freelance Site Feasibility Specialist – remote

Location: Europe (remote)

Contract type: Freelance

FTE: 1.0 - full time

Start: immediately

Duration: around 3 months

About the Role

We are seeking a Freelance Site Feasibility Specialist to support the successful identification and selection of investigator sites across Europe. This role is highly operational and site-facing, focusing on feasibility outreach, data collection, and tracking , while ensuring high standards of communication, organization, and confidentiality. You will work closely with internal study teams and external sites to gather key information that supports efficient study start-up and site selection.

Key Responsibilities

Conduct site-facing outreach to investigators and study sites across Europe

Distribute feasibility questionnaires and follow up to ensure timely responses

Act as a key point of contact for feasibility-related communication

Support the collection of feasibility data (SSQ, site information, etc.)

Track responses and maintain accurate records in internal systems

Ensure timely reporting of feasibility status to stakeholders

Assist with data entry and monitoring of feasibility responses

Coordinate and support the collection of Confidentiality Disclosure Agreements (CDAs)

Ensure proper tracking and documentation of all agreements

Maintain compliance with internal processes and timelines

Maintain clear and professional communication with sites and internal teams

Collaborate with study start-up, site identification, and project teams

Provide regular updates on feasibility progress and any challenges

Requirements

Experience in: Clinical research (CRO, pharma, biotech)

Minimum of 2-3 years in site feasibility, site ID, or study start-up

Strong organizational and tracking skills

Excellent communication skills (written and verbal)

Experience working with: Feasibility questionnaires (SSQ) and CDA collection processes

Ability to manage multiple sites and timelines simultaneously

Fluent in English (additional European languages are a plus)

If this role sounds of interest, please apply today!

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is zł105,900.00 - zł196,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

REQUIRED VERIFIED SKILLS

Clinical Research
Excel
Data Entry

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Site Feasibility Specialist - Freelance position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Career path typically progresses from Associate, to Senior Specialist, and eventually to Manager or Lead positions within the department.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: Clinical Research, Excel, Data Entry. Prepare real-world examples demonstrating these skills for the interview.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.