Clinical Project Manager (FSP) (Remote)

RWE Clinical Project Manager (FSP)

Job Overview

IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team working fully within the environment of a prominent pharma this role the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within three different therapeutic areas (oncology virology inflammation). It is important for this individual to have experience working in observational research across primary and secondary data collection study designs as well as leading clinical studies independently.

Who do you work with

• Epidemiologists data science and clinical leads to deliver project specific goals and timelines
• Vendors to communicate status of deliverables and workflow
• Program and business leads to manage full portfolio of projects

What are you great at

• Independently executing observational and real-world studies while balancing speed quality and cost
• Leading cross-functional teams to achieve milestones and resolve study issues
• Proactively identifying risks and implementing mitigation plans
• Communicating clearly with stakeholders including preparing and presenting project updates to leadership
• Good understanding of project financials including experience managing contractual obligations and implications
• Driving operational excellence and strategic partnership with clients
• Managing vendors effectively across different sourcing models (in-house hybrid outsourced)
• Bringing clarity to complex or ambiguous situations and making informed decisions
• Results-oriented approach to work towards delivery and output
• Strong organizational prioritization and time management skills
• Ability to operate effectively in a matrixed fast-paced and evolving environment

Your responsibilities may include:

• Leading global cross-functional observational study teams and owning delivery of contracted scope timelines and quality
• Developing study documentation including project management plans
• Ensuring consistent use of study tools training materials and compliance with SOPs policies and procedures
• Monitoring study progress and financial performance; supporting forecasting and change control as needed
• Lead project vendor management related activities and communications per project requirements
• Anticipating operational and quality risks responding to issues raised by the project team and planning/implementing appropriate corrective or preventative actions
• Generating project- or program-level metrics and reports for senior management
• Capturing lessons learned and contributing to continuous improvement and best practices

Required knowledge skills and abilities

• Bachelors degree in life sciences or related field
• Minimum 4-6 years of experience in project management and/or clinical operations within pharma CRO or RWE environment (or equivalent combination of education training and experience)
• Demonstrated experience leading observational or real-world evidence studies
• Strong understanding of RWE study designsand clinical research conduct and skill in applying applicable clinical research regulatory requirements
• Experience with primary and secondary data study designs
• Therapeutic area expertise desired (oncology virology inflammation)

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

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. 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.