Clinical Community Analyst

IQVIA

Warszawa

On-site

PLN 71,000 - 230,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

IQVIA is seeking a Clinical Community Analyst to join the iPOST Team in Warsaw, Poland. You will oversee Investigator Portals from start-up to archive, coordinating site engagement strategies and portal communications to ensure a positive experience for clinical study sites worldwide.

You will partner with study teams and vendors, manage content and communications, and support portal operations with strong project management and cross-cultural collaboration skills.

Qualifications

  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or related field.
  • Experience in clinical research, including Clinical Trial Coordination and/or Clinical Trial Monitoring with Investigator Portals or site engagement platforms.
  • Strong organizational and project management skills.
  • Excellent written and verbal communication skills.
  • Advanced Microsoft Office skills, including data analysis and reporting.
  • Ability to work effectively in global, cross-functional, and multicultural teams.

Responsibilities

  • Serve as primary operational contact for Investigator Portals from study start-up through archive.
  • Develop and implement site engagement and communication strategies with study teams.
  • Coordinate portal launches and ongoing activities with study teams and portal vendors.
  • Manage and maintain portal content, including News posts, Email communications, Enrollment dashboards, Visit guides and calculators.
  • Edit and publish communications related to study updates and activities.
  • Provide business application and portal support to study teams.
  • Facilitate kickoff meetings and ongoing portal review meetings with cross-functional study teams.
  • Escalate portal-related issues when appropriate and coordinate resolution across impacted teams.
  • Support user management activities and vendor interactions.

Skills

Project management
Communication skills
Microsoft Office
Data analysis
Team collaboration
Clinical research
Investigator Portals
Vendor coordination
Stakeholder engagement

Education

Bachelor's degree in Life Sciences / Health Sciences / Nursing / Pharmacy

Job description

About the Role

IQVIA is seeking a Clinical Community Analyst to join iPOST Team. This team is responsible for the creation, management, and retirement of study-specific investigator portals that support engagement, communication, and collaboration with clinical study site personnel globally. In this role, you will partner with study teams and portal vendors to implement site engagement strategies, manage portal content and communications, support portal operations, and ensure a positive experience for investigative sites throughout the lifecycle of a clinical trial. This is an excellent opportunity for a clinical research professional who enjoys project management, stakeholder engagement, digital communications, and technology-driven solutions within clinical trials.

Key Responsibilities
  • Serve as the primary operational contact for study-specific Investigator Portals from study start-up through archive.
  • Partner with study teams to develop and implement site engagement and communication strategies.
  • Coordinate portal launches and ongoing activities with study teams and portal vendors.
  • Manage and maintain portal content, including: News posts, Email communications, Enrollment dashboards, Visit guides and calculators
  • Edit and publish communications related to study updates and activities.
  • Provide business application and portal support to study teams.
  • Facilitate kickoff meetings and ongoing portal review meetings with cross-functional study teams.
  • Escalate portal-related issues when appropriate and coordinate resolution across impacted teams.
  • Support user management activities and vendor interactions.
Qualifications
  • Required Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related field.
  • Experience in clinical research, including: Clinical Trial Coordination, and/or Clinical Trial Monitoring Experience supporting studies utilizing Investigator Portals or site engagement platforms.
  • Strong organizational and project management skills.
  • Excellent written and verbal communication skills.
  • Advanced Microsoft Office skills, including data analysis and reporting capabilities.
  • Ability to work effectively in global, cross-functional, and multicultural teams.
Preferred
  • Experience creating study newsletters, email campaigns, and site-facing communications.
  • Experience with portal administration, community management, or other digital engagement platforms.
  • Knowledge of clinical trial processes and study lifecycle activities.
  • Experience working directly with vendors and technology platforms supporting clinical research.
About IQVIA

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 zł71,300.00 - zł230,300.00. 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Scientist, Clinical Science, Cronos
Clinical Scientist, Clinical Science, Cronos

IQVIA • Warszawa

On-site
PLN 143,000 - 265,000
Senior Clinical Project Manager
Senior Clinical Project Manager

IQVIA • Warszawa

On-site
PLN 218,000 - 405,000
Reg & Start Up Spec 2
Reg & Start Up Spec 2

IQVIA • Warszawa

On-site
PLN 151,000 - 281,000
Centralized Monitoring Lead- Sponsor Dedicated
Centralized Monitoring Lead- Sponsor Dedicated

IQVIA • Warszawa

On-site
PLN 151,000 - 281,000
Clinical Supply Coordinator
Clinical Supply Coordinator

IQVIA • Warszawa

On-site
PLN 115,000 - 213,000
CPM/Sr CPM, IQVIA Biotech CVRM
CPM/Sr CPM, IQVIA Biotech CVRM

IQVIA • Warszawa

On-site
PLN 218,000 - 405,000
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership - Poland
Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership - Poland

IQVIA • Warszawa

On-site
PLN 226,000 - 419,000
Senior Clinical Research Associate, Sponsor dedicated in Poland
Senior Clinical Research Associate, Sponsor dedicated in Poland

IQVIA • Warszawa

On-site
PLN 172,000 - 376,000
Home-office
Company car
Flexible schedules
Global Senior Trial Delivery Manager - Sponsor Dedicated
Global Senior Trial Delivery Manager - Sponsor Dedicated

IQVIA • Warszawa

On-site
PLN 242,000 - 405,000
Health insurance
Clinical Research Associate - IQVIA Biotech Poland
Clinical Research Associate - IQVIA Biotech Poland

IQVIA • Warszawa

On-site
PLN 133,000 - 280,000