IPOST Clinical Community Analyst
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 13h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 28d ago
The date the source published, not the day we noticed it (2026-09-04). Last seen at its source just now.
We have tracked this listing since 21 Sep 2026 (10 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Poland
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $1,388–1,938/mo
Middle 50% of 10 listings that do state pay — Content & Media · all levels · EMEA · USD/month. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 10d ago · last seen just now
- location not stated
The listing
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.
ICON is seeking an iPOST Clinical Community Analyst to join our global Investigator Portal Operations Team.
This role is focused on supporting investigator and site engagement across clinical trials through the management of study-specific investigator portals. Working closely with study teams, site personnel, vendors, and internal stakeholders, you will help deliver effective communication, engagement strategies, and portal operations that enhance the study site experience throughout the trial lifecycle.
We are interested in speaking with individuals who have experience working within clinical research and have hands-on experience using investigator portals or similar site engagement platforms. Experience may have been gained from a CRO, pharmaceutical, biotechnology, sponsor, site, or vendor environment.
Key Responsibilities
- Manage investigator portals from study start-up through study close-out and archiving.
- Partner with study teams to develop and implement site engagement and communication strategies.
- Create, maintain, and publish portal content including news posts, communications, surveys, forms, dashboards, and study resources.
- Coordinate portal launches and ongoing portal activities with study teams and external vendors.
- Support portal user management and provide business support to stakeholders.
- Lead and facilitate meetings with study teams related to portal planning, implementation, and ongoing study conduct.
- Monitor portal activity and engagement, identifying opportunities to improve the site experience.
- Investigate, track, and resolve portal-related issues, escalating when appropriate.
- Contribute to process improvements, training activities, operational documentation, and best practice development.
- Support broader site engagement initiatives and technology-related projects as required.
What We're Looking For
- Degree in Life Sciences, Health Sciences, or equivalent relevant experience.
- Experience working within clinical trials or clinical research.
- Experience using investigator portals or similar clinical technology platforms that support study sites and investigators.
- Strong understanding of clinical trial processes and study conduct.
- Excellent organisational and project coordination skills with the ability to manage multiple activities simultaneously.
- Strong written and verbal communication skills.
- Experience creating communications, newsletters, site-facing content, or engagement materials.
- Advanced Microsoft Office skills, including the ability to analyse and present information effectively.
- Ability to work successfully within global, cross-functional teams.
Preferred Experience
- Experience supporting global or multi-regional clinical trials.
- Experience working directly with study teams, investigators, sites, or clinical technology vendors.
- Experience delivering training, onboarding, or user support.
- Knowledge of site engagement strategies and change management principles.
- Additional language skills would be advantageous.
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