IQVIA

Clinical Research

• Prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures.
• Interpret analyses and write statistical sections of study reports.
• Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy.
• Conducts all appropriate validation requirements, according to Standard Operating Procedures (SOPs), for each task undertaken.
• Checks programming logs for cleanliness and correct processing of data.
• Inputs into Data Issues log and follows issues to appropriate resolution.
• Perform statistical team lead role on single studies.
• Works closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget.
• Build and maintain effective customer relationships, driving statistical discussions, providing support and/or guidance for statistical activities.
• Acts as a lead in meetings, documenting where necessary and following up on actions.
• Actively participates in internal project team meetings.
• Plans and documents timelines, forecasts resource needs, suggests work that may be out of scope.
• Shares accountability for the financial success of assigned studies.
• Identifies risks to project delivery and/or quality and proposes solutions to mitigate risks.

Biostatistician 2

Manager

• The Associate SAM leads and oversees our country operations teams ensuring that our client commitments are delivered timely and according to project scope and processes.
• Interaction with the project manager, clinical lead, regulatory and contract and budget solution advisors, and country regulatory specialists.
• Participation in pre-award and big defense meeting activities providing start-up expertise input for the project strategy.
• Develop the site activation delivery strategy according to project scope and specifics.
• Oversee the execution of global site activation strategy.
• Communication with client, project team members, and local regulatory specialists on study sites status, activation projections, risks, and opportunities.

Assoc. Site Activation Manager – Sponsor Facing

Medical writer

• Lead the development of high-quality clinical and regulatory documents (e.g., Investigator’s Brochures, Clinical Study Reports, clinical summaries, and marketing authorization submissions) in compliance with global regulatory guidelines (ICH, FDA, EMA) and internal standards
• Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs
• Provide strategic guidance to cross-functional teams on document content, messaging, and regulatory positioning to ensure alignment with program goals
• Manage medical writing projects, including planning, timelines, resource coordination, and delivery to ensure milestones and submission deadlines are met
• Collaborate with cross-functional stakeholders (Clinical, Regulatory Affairs, Biostatistics, Safety, etc.) to gather, interpret, and accurately present clinical data
• Mentor and support other medical writers, ensuring high-quality, scientifically sound, and consistent deliverables across projects
• Review and edit project-related documents to ensure accuracy, clarity, consistency, and compliance with templates and style guides
• Attend project and team meetings to provide expert input on document development, study data interpretation, and process improvements
• Contribute to and lead process improvement initiatives to enhance efficiency, quality, and consistency in document preparation
• Develop, maintain, and refine standard operating procedures (SOPs), templates, and best practices for medical writing
• Stay current with evolving global regulatory requirements, industry trends, and therapeutic area knowledge to ensure compliance and innovation.

Principal Medical Writer

Strategy

• Develop and implement delivery strategies during the RFP/Bid Defense cycle
• Collaborate with Sales, Medical, Operations, and provide guidance for tailor-made strategies
• Scan therapeutic and operational landscape to develop long term implementation strategies
• Act as champion for project centricity and enable the project delivery team
• Guide and mentor Project Leader to present strategy to clients and internal stakeholders
• Support Sales in preparation for customer and bid defense meetings
• Identify quality issues within the study and provide coaching on resolution

Therapeutic Strategy Lead – Internal Medicine, Immunology

Technical Project Manager

• Serve as a strategic technical leader responsible for bridging business objectives and engineering execution
• Define and maintain end-to-end system architecture across applications
• Drive end-to-end delivery of complex, cross-functional technical programs
• Establish and enforce integration standards, architectural governance, and documentation practices
• Build strong relationships across business and technical stakeholders

Senior Technical Project Manager

Business Operations

• Partner with the Product Manager to run discovery: stakeholder interviews, workflow mapping, pain-point analysis, and scope definition for data delivery, client access, analytics, and administration capabilities.
• Support product discovery activities: problem statements, success metrics, MVP scope, and release phasing recommendations.
• Author and maintain business requirements, functional specifications, and user stories with testable acceptance criteria aligned to the team’s delivery model.
• Participate in backlog refinement, sprint planning, demos, and retrospectives; capture decisions and change logs.
• Triage clarification requests during development; escalate scope or policy conflicts to the Product Manager with options and impact.
• Contribute to release notes and internal enablement materials for operations and client-facing teams.
• Facilitate working sessions with engineering, architecture, security, operations, and client success.

Associate Director, Business Systems

Research Analyst

• Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with contracted scope of work, GCP, and ICH guidelines
• Collaborate with site staff to implement and track subject recruitment strategies
• Deliver protocol and study-specific training to site personnel
• Assess site performance and adherence to the protocol
• Monitor study progress by tracking regulatory submissions and subject enrollment
• Ensure that essential documents are collected and maintained in accordance with regulatory standards
• Document site management activities, visit outcomes, and follow-up actions
• Work closely with cross-functional project teams to support study execution

Clinical Research Associate

Account Executive

• Promote products in the Endocrinology/Diabetes space
• Achieve sales forecast and gain adoption and utilization of the product portfolio
• Establish mutually beneficial business relationships with targeted accounts and physicians
• Coordinate sales strategies with appropriate teammates to maximize sales in assigned territory

Inside Sales Representative – Diabetes

Risk

• Serve as the primary IQVIA Digital representative on enterprise data governance committees and boards
• Lead data governance and compliance initiatives in close partnership with IQVIA Information Governance
• Ensure consistent application of data governance, compliance, and documentation standards across IQVIA Digital data management and products
• Develop, implement, and document cross-organization operating models, including Standard Operating Procedures (SOPs), Business Requirement Documents (BRDs), workflow diagrams (e.g., Lucidchart), and governance frameworks
• Create, standardize, and operationalize Data Use Agreements (DUAs), Data Dictionaries, Data Catalogs, and related governance artifacts
• Drive operational efficiency through standardization, clear documentation, and scalable enablement practices
• Own and evolve the Data Management SharePoint site as the authoritative source for design, processes, and documentation
• Develop high-quality, executive-ready materials for senior leadership, governance committees, and external stakeholders
• Translate complex technical and regulatory concepts into clear, actionable guidance for cross-functional teams

Associate Director, Governance, Data Management Operations Enablement

IT Support

• Provide Tier 1 support in a Helpdesk environment
• Identify requests from end-users
• Categorize and record reported queries and provide solutions
• Support problem identification
• Process user account creation, modification, and deactivation
• Perform identity verification and entitlement validation prior to executing requests
• Maintain and update user access across systems such as directory services, applications, and client platforms
• Ensure compliance with least privilege principles and client security requirements
• Escalate unresolved problems to a higher level of support
• Manage customer service or service desk functions
• Act as a point of contact for support service users and customers
• Log, categorize, and prioritize requests according to classification standards
• Ensure adherence to Service Level Agreements (SLA)

Tier 1 Helpdesk Support, English-Speaking

• Associate Clinical Project Managers are an integral part of clinical trial delivery
• Liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster
• Supporting the efforts of CPM to drive operational excellence and strategic leadership

Associate Clinical Project Manager – Trial Vendor Manager

Software Engineer

• Under general supervision, responsible for developing and preparing high‑quality budgets and proposals for assigned customers
• Review Requests for Proposal (RFPs) to identify required information for proposal text and budget development
• Collaborate closely with the business development team to prepare and finalize submissions
• Develop proposal narratives and cost budgets for new proposals, re‑bids, change orders, and related documents
• Revise or develop preliminary agreements and related budgets
• Ensure scope of work is clearly defined and budgets accurately reflect agreed scope
• Develop and maintain an understanding of all processes, policies, and guidelines relating to proposal development
• Participate in strategic discussions and calls to clarify customer requirements
• Perform quality control reviews and edits on proposal documents
• Support the finalization and distribution of proposal documents

Proposal Developer I

Analyst

• Manage single and multi-service projects, ensuring quality deliverables on time
• Provide expert skills as part of a Clinical Data Management (CDM) team
• Serve as internal or external point of contact on standalone coding studies or accounts
• Maintain post-coding dictionary up-versioning synonym and coding reconciliation
• Perform Dictionary up-versioning activities
• Perform external verbatim coding of data from non-EDC sources
• Perform comprehensive quality control procedures
• Perform Serious Adverse Event (SAE) coding reconciliation activities
• Collaborate with customers and develop solutions and action plans for issues
• Proactively identify, solve quality issues and deliver projects as per agreed timeline
• Identify and implement processes and quality improvement initiatives
• Provide review and expert opinion in developing, revising, and maintaining standard operating procedures
• Develop and maintain good communications and working relationships with the CDM team and client stakeholders

Clinical Coding Analyst

Business Development Rep

• Drive enterprise-level growth for IQVIA’s Technology-Enabled Sales Organization (TESO) by developing and closing complex, integrated commercial solutions.
• Serve as a senior client partner to pharmaceutical and biotech companies.
• Own the full business development lifecycle—from opportunity creation through deal close.
• Build executive-level relationships, shape client strategy, and position differentiated, outcome-driven solutions.
• Identify, shape, and close complex, multi-solution deals across IQVIA’s commercial portfolio.
• Lead the end-to-end sales process with strong pipeline discipline and deal quality focus.
• Develop and execute strategic account plans to drive growth and expand client partnerships.

Senior Director, Business Development

• The Primary Care Sales Representative is responsible for driving strong brand performance by effectively engaging targeted health care providers and key accounts within an assigned territory.
• This role executes against sales objectives, brand KPIs, and financial targets by delivering a compelling and differentiated value proposition while building trusted, long‑term customer relationships.
• Develop and implement an effective call plan to meet call metrics, ensuring optimal coverage and frequency with key customers to maximize access and sales potential.
• Clearly articulate the client value proposition to assigned healthcare providers, and identify, engage, and maintain relationships with disease state experts and speakers/advocates to optimize brand performance.
• Prepare pre-call strategies using SMART objectives and conduct post-call evaluations to drive continuous improvement in sales performance.