Clinical Community Analyst

IQVIA Argentina; Warszawa; On-site; PLN 71,000 - 230,000; Full time

Job summary

IQVIA is seeking a Clinical Community Analyst to join iPOST Team. This role focuses on creating, managing, and retiring study-specific Investigator Portals that support engagement, communication, and collaboration with clinical study site personnel globally.

You will partner with study teams and portal vendors to implement site engagement strategies, manage portal content and communications, and ensure a positive experience for investigative sites throughout the lifecycle of a clinical trial.

Qualifications

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

Responsibilities

• Serve as the primary operational contact for study-specific Investigator Portals from 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 such as 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 and review meetings with cross-functional study teams.
• Escalate portal-related issues and coordinate resolution across involved teams.
• Support user management and vendor interactions.

Skills

Project management

Written and verbal communication

Organizational skills

Cross-functional collaboration

Multicultural teamwork

Clinical research experience

Investigator Portals experience

Education

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

Tools

Microsoft Office

Data analysis & reporting

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.

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.