Latest Openings at IQVIA

The Clinical Project Manager / Senior Clinical Project Manager role requires you to manage cross functional teams and liaise directly between IQVIA functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best in class technology and data analytics.

Key collaborators are the, the Project Management Analyst for project coordination, tracking and financial analysis, the CRA for site coordination, Medical Advisor for subject safety oversight and the Data Team Lead, Biostatistician and Pharmacokineticist for analysis and reporting.This is an important and high-profile role within our Research & Development Operation and IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career.

Typically assigned to one or two projects, or a program, responsibilities might include:

• Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope
• Serving as the primary contact with the customer for progress and governance.
• Managing the Phase I or Investigator site(s)
• Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures
• Anticipating risk and implementing mitigation strategies
• Managing study team assignments, accountability and resource requirements
• Ensuring the study budget is managed proactively including scope changes and financial systems are accurate

Required Knowledge, Skills And Abilities

• Bachelor's degree in life sciences or related field and 5 years’ clinical research experience
• Global project management experience within the drug development industry, with previous CRO experience is ideal.
• Minimum 2 years prior project management experience and experience in clinical operations; or equivalent combination of education, training and experience
• In depth knowledge of early phase study designs, clinical pharmacology, pharmacokinetics, pharmacodynamics and therapeutic knowledge in any of the following areas would be an advantage: neuro-degenerative, psychiatric or dermatological disorders; vaccines

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Job Overview
Provide programming support as part of the Statistical Programming (SP) team to develop and maintain programs to meet internal and external clients’ needs. Support the development of project-related solutions to a variety of statistical programming tasks.

Essential Functions

• Program, test, and document statistical programs for use in creating statistical tables and listing summaries.
• Program analysis databases (derived datasets) and transfers of data for internal and external clients.
• Program database quality control checks.
• Assist in development of programming documentation including plans and specifications, as appropriate.
• Assist in developing, implementing and validating new process technologies, macros and applications.
• Assist project lead in fulfilling project responsibilities.

Qualifications

• Bachelor's Degree Computer science or related field Req
• Equivalent combination of education, training and experience in lieu of degree Req
• Basic knowledge of statistics and/or clinical drug development process
• Basic knowledge of statistical computing applications such as Base SAS, SAS/STAT and SAS Macro Language
• Organizational and communication skills
• Ability to effectively handle multiple tasks
• Aptitude for mathematical calculations
• Accuracy and attention to detail
• Ability to establish and maintain effective working relationships with coworkers, managers and clients

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Job Overview
Independently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site Manager, and/or a leadership role in a specific CDM task (e.g. Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.

Responsibilities

Client Management:

• Serve as primary point of contact for customer on data management deliverables
• Manage multiple large studies or program of studies (possibly global)
• Provide leadership and senior support to DTLs on multiple large global studies/programme of global studies
• Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
• Lead direct negotiations with customer, e.g., timelines, financial, process, resources.
• Maintain strong customer relationships
• Ensure open communications with customer and IQVIA management to independently manage and meet contractual obligations

Service Management:

• Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
• Provide training and development on data management expertise to junior team members
• Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders
• Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
• Serve as the escalation point for unresolved data issues
• Independently work with client data managers, vendors, internal team members for resolution
• Ensure appropriate resources are assigned to meet project deliverables
• Create and/or review and sign-off on all data management plan (DMP) documents
• Ensure service and quality meet agreed upon specifications per the DMP and contract/SOW
• Implement proactive quality management plans across multiple projects/programmes/customer account. Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
• Continuously look for opportunities to improve service
• Develop and work with team to implement plan to re-organize and drive change (possibly across a customer account)
• Ensure timely follow-up and resolution of compliance issues
• Serve as Subject Matter Expert (SME)
• Provide leadership and expertise in a specific CDM task or technology
• Serve as customer site lead for one or more customers
• Train and mentor junior DTL staff in DM expertise
• may coordinate the work of more junior DTL staff
• Independently maintain internal tracking databases and systems

Financial Management/Business Development Support:

• Independently manage SOW/budget
• Review financial reports on a monthly basis and participate in project reviews as requested
• Identify out of scope tasks and track change orders to completion
• Participate in pricing discussions across customer account
• Serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing
• Independently support RFP process (review RFP documents, pricing, attend bid defense)

Other:

• Independently bring process improvements and solutions to the CDM team/CDM department
• Lead a focus team or global or local best practice team
• Communicate lessons learned and/or present in CDM workshop(s)
• Manage the development and implementation of new technology or tool
• Present at professional conferences and/or publish articles in professional journals
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
• Perform other duties as directed by the functional manager

Minimum Required Education And Experience

• Bachelor's Degree in health, clinical, biological or mathematical sciences, or related field
• 5 - 7 years direct Data Management experience, including 5 or more years as a CDM project lead.
• Equivalent combination of education, training and experience.

Skills And Abilities

• Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients).
• Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation, management of local laboratory data, and/or new technology).
• Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently.
• Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology.
• Knowledge of operating procedures and work instructions and the ability to apply them in practice.
• Knowledge of Good Clinical Practices and relevant regulatory guidelines.
• Excellent communication, interpersonal, customer service, and teamwork skills.
• Excellent organizational and problem-solving skills.
• Excellent project management skills.
• Ability to work independently.
• Comprehensive understanding of clinical drug development process.
• Ability to establish and maintain effective working relationships with co-workers, managers and customers.