PROJECT COORDINATOR, STUDY OPERATIONS, CRONOS-PCS

The PCS team leads the industry in the science of measuring the patient experience.
We pair strategic consulting expertise with technical scientific knowledge to design and execute scientifically rigorous research that incorporates the patient voice into the development and commercialization of new medicines.
This research includes qualitative (e.
., patient interviews, focus groups), quantitative (e.
., clinical outcome assessments (COAs)/patient-reported outcomes (PROs), preference research) and passive (e.
., digital health technology tools) approaches to understand patient, caregiver and physician experiences and expectations of disease and treatment.
Role & Responsibilities As a Project Coordinator, Study Operations within the PCS team at IQVIA, you will work to assist Project Managers and teams with the coordination of resources, equipment, meetings, clinical reviews and information.
Project Coordinators support the organization of projects with the goal of getting them completed on time.
Responsibilities include.
Coordinate activities and resources in support of the project team for multiple projects simultaneously.
Interact with internal departments including operations, data management, and clinical to execute daily tasks associated with providing clinical data management to the sponsored pharma industry research trials.
Support the project team during study start-up, maintenance, and close-out phases.
Execute and test data transfers to ensure internal and sponsor technical requirements are met.
Manage Site, Sponsor and study related inquiries and escalate to Project Manager and/or client as necessary.
Interact with sites to schedule calls.
Prepare client data to facilitate clinical analysis in the timelines specified.
Attend and participate in internal team meetings as well as external meetings with sponsors.
Prepare, review and/or edit meeting minutes, presentations, reports and tables.
Work with local site and sponsor teams globally to initiate and facilitate communication between Clinical Specialists and site raters.
Navigate complexity and logistics of global working teams.
Alert appropriate team members of potential timing and resource issues.
Required Knowledge, Skills And Abilities Proven problem-solving skills with strong attention to detail.
A self-starting mind-set with excellent team-based interpersonal skills with the ability to work independently with the full spectrum of our people.
Strong computer skills, including Microsoft Office applications Ability to build strong business relationships and influence with key stakeholders at all levels within the business.
Ability to rapidly assimilate multiple types of information from a variety of sources for effective decision making.
Excellent written and oral communication skills including grammatical/technical writing skills.
Excellent attention and accuracy with details.
Ability to confidently communicate with and effectively present information to internal team.
Must be able to work in a fast-paced environment with demonstrated ability to effectively manage multiple tasks and projects.
Strong individual initiative.
Strong organizing skills.
Strong commitment to quality.
Ability to work within a team environment.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
What will help you to stand out.
Background in CNS (Central Nervous System) or experience in CNS clinical trials Experience with COA (Clinical Outcome Assessments) or ClinRO (Clinician Reported Outcome) Experience with IRB (Investigator Review Board) submissions Project Management experience Advanced English level IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
Learn more at https://jobs.
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