Non-Interventional Study Research Manager

Non-Interventional Study Research Manager
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Non-Interventional Study Research Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs

What You Will Do:

Under the supervision of the Associate Director, you will lead operational activities related to study planning, study execution, and the summarization of results from observational research studies and related activities.

Key responsibilities include:

- Coordinates the end-to-end process for executing observational or non-interventional research studies, in compliance with Good Pharmacoepidemiology Practice (GPP) and CORE Standard Operating Procedures (SOPs).
- Plans, initiates, executes, and closes out primary data collection, chart review, database, and molecular epidemiology studies in addition to other activities (e.g., literature reviews, dossier development, economic modelling support, etc.)
- Collaborates with colleagues across CORE, Global Medical and Scientific Affairs (GMSA) to support the lead scientists (from GMSA) in overall operational support for study conduct.
- Provides study-level management support, which includes facilitation of the execution of appropriate service for approved proposals/scopes of work (including the review of requests for information/proposal, draft scope of work, where applicable), confidentiality and consultant agreements, and subsequent amendments/change orders.
- Participates in protocol and interim/final report preparation and literature review abstraction and summarization.
- Coordinates the review and finalization of all vendor documents, such as the safety management, data management, communication, project management, and validation plans  Tracks study timelines and deliverables and follows up on action items.
- Collaborates extensively and troubleshoots issues by providing potential resolutions (when necessary) with internal and external partners, ensuring timely study management and execution  Assists in tracking study milestones and timelines.
- Liaises with outsourced vendors and cross-functional teams to communicate and oversee project status and/or needs.
- Participates in quality control assessments and ensures integrity of study data for reports and publications.
- Understands, coordinates, and documents adherence to internal, external, and regulatory compliance requirements.
- Utilizes, manages, and maintains document repositories and internal/external systems (e.g., REV OPS, Engage Zone, Veeva Vault).
- Provides operational support for due diligence checks, site contract and budget review/approval, informed consent, study registration, IT and/or privacy assessments, vendor qualification, adverse event reporting and reconciliation, and publication submissions.
- Manages poster and publication development, including formatting, medical writing, figure/data content development, co- author review, internal review process

Your Profile:

- Two or more years of work experience within clinical/observational research or equivalent experience.
- Excellent communication and interpersonal skills and the ability to collaborate with and influence a wide variety of stakeholder.
- Basic knowledge of epidemiologic or outcomes research.
- Fluency in English (written and spoken)
- Strong project management and prioritization skills.
- High level of motivation and ability to work independently and collaboratively.

Required qualifications and experience:

- University degree in medicine, science, or equivalent combination of education & experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- Willingness to travel as required (approximately 25%)

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