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 Manager, Data Management, you will provide operational and people leadership to Clinical Data Coordinators (CDCs), Clinical Data Management Specialists (CDMSs), and other Data Management professionals within ISS. You will be accountable for the successful delivery of data management services, ensuring that quality, timelines, productivity, compliance, and client expectations are consistently achieved.
The role requires strong leadership, strategic oversight, and stakeholder management capabilities, with responsibility for team development, operational excellence, resource planning, and the promotion of continuous improvement initiatives. The Manager serves as a key representative of ISS Data Management both internally and externally, fostering strong client relationships and advancing the function's capabilities and reputation.
Key Responsibilities- Provide effective line management, leadership, coaching, and mentorship to Data Management teams across assigned projects and functions.
- Foster a high-performance culture focused on accountability, collaboration, quality, innovation, and continuous learning.
- Conduct performance evaluations, career development discussions, and succession planning activities for direct reports.
- Identify capability gaps and implement development plans to support individual and team growth.
- Support talent acquisition activities, including interviewing, onboarding, workforce planning, and resource management.
- Mentor future leaders and technical experts within the organization.
- Oversee the delivery of Data Management activities to ensure compliance with agreed timelines, quality expectations, and budget requirements.
- Ensure accurate resource allocation and workload distribution across teams to optimize productivity and delivery outcomes.
- Monitor key operational metrics, productivity indicators, quality trends, and capacity forecasts, implementing corrective and preventive actions as needed.
- Effectively manage project risks, issues, and escalations, ensuring timely resolution and stakeholder communication.
- Ensure all deliverables meet regulatory requirements, sponsor expectations, and internal quality standards.
- Maintain compliance with ICH-GCP, regulatory requirements, sponsor requirements, and applicable ICON Standard Operating Procedures (SOPs).
- Promote a culture of quality and inspection readiness across all Data Management activities.
- Represent Data Management during internal audits, sponsor audits, regulatory inspections, and quality reviews.
- Ensure audit observations and corrective actions are addressed appropriately and closed within agreed timelines.
- Drive adherence to quality management processes and continuous process improvement initiatives.
- Promote adoption of innovative technologies, automation opportunities, and data-driven solutions to enhance efficiency and quality.
- Contribute to the development and standardization of departmental processes, tools, and methodologies.
- Support organizational transformation initiatives aligned with strategic business objectives.
- Act as a trusted partner to clients and sponsors by maintaining strong professional relationships and ensuring high-quality service delivery.
- Provide leadership and strategic input during client meetings, governance reviews, and operational discussions.
- Proactively communicate project status, risks, mitigation plans, and operational updates to key stakeholders.
- Maintain a strong understanding of evolving industry trends, emerging technologies, regulatory expectations, and best practices within Clinical Data Management.
- Serve as a knowledgeable ambassador for ISS Data Management during client visits, business development discussions, conferences, industry forums, audits, and inspections.
- Effectively articulate ISS Data Management capabilities, operational strengths, quality frameworks, and innovation initiatives to internal and external stakeholders.
- Contribute to strengthening the market presence and reputation of ISS Data Management through thought leadership and client engagement.
- Support ISS operational activities including employee onboarding, contingent workforce management, freelancer oversight, and associated operational processes.
- Manage competing priorities effectively while ensuring optimal team performance and service delivery.
- Perform additional duties and strategic initiatives as required to support organizational objectives.
- Significant Clinical Data Management experience across the full clinical trial lifecycle.
- Extensive experience working with multiple EDC systems, data review platforms, and clinical reporting tools.
- Minimum of 2 years of people management experience, including performance management, workforce planning, recruitment, coaching, and career development.
- Demonstrated experience managing project delivery, operational metrics, and cross-functional stakeholder relationships.
- Experience supporting client engagements and sponsor interactions.
- Previous experience managing Team Leads or equivalent supervisory roles.
- Experience leading global or multi-functional teams within a matrix environment.
- Exposure to process improvement, quality management systems, and operational excellence initiatives.
- Strong understanding of GCP, ICH guidelines, regulatory requirements, and clinical data management best practices.
- Proven leadership and decision-making capabilities.
- Excellent project management, planning, and organizational skills.
- Ability to effectively manage multiple priorities within a dynamic and evolving environment.
- Strong analytical and problem-solving skills.
- Excellent verbal, written, presentation, and stakeholder management skills.
- Demonstrated ability to influence, collaborate, and build relationships at all organizational levels.
- High attention to detail and commitment to quality.
- Ability to work effectively under pressure while maintaining focus on quality and delivery commitments.
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
Skills Required
- Significant clinical data management experience across the full clinical trial lifecycle
- Extensive experience with multiple EDC systems, data review platforms, and clinical reporting tools
- At least 2 years of people management experience, including performance management, workforce planning, recruitment, coaching, and career development
- Experience managing project delivery, operational metrics, and cross-functional stakeholder relationships
- Experience supporting client engagements and sponsor interactions
- Previous experience managing Team Leads or equivalent supervisory roles
- Experience leading global or multifunctional teams within a matrix environment
- Exposure to process improvement, quality management systems, and operational excellence initiatives
- Strong understanding of GCP, ICH guidelines, regulatory requirements, and clinical data management best practices
- Proven leadership and decision-making capabilities
- Excellent project management, planning, and organizational skills
- Ability to manage multiple priorities in a dynamic environment
- Strong analytical and problem-solving skills
- Excellent verbal, written, presentation, and stakeholder management skills
- Ability to influence, collaborate, and build relationships across organizational levels
- High attention to detail and commitment to quality
- Ability to work effectively under pressure while maintaining quality and delivery commitments
- Legal right to work in the country where the role is based
ICON plc Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.
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Healthcare Strength — Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
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Leave & Time Off Breadth — Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
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Retirement Support — Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.
ICON plc Insights
What We Do
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
