IQVIA

Medical writer

• Acts as Lead Medical Writer on most types of writing projects
• Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements
• Performs Senior Review of straightforward medical writing deliverables
• Negotiates timelines and discusses/resolves customer comments
• Provides written and verbal feedback to junior staff, and to customers when appropriate
• Keeps abreast of current medical and/or technical writing/regulatory knowledge
• Take a leading role in preparing assigned documents
• Plan and organize workload for assigned projects and tasks
• Lead meetings on more challenging topics independently
• May assist in the training and development of junior staff
• May act as Project Manager for a more complex but single Medical Writing project

Senior Medical Writer

Director

• Manages a department or small unit.
• Provide leadership and advice on the development of optimum strategies for drug development, product lifecycle management and portfolio management to meet pharmaceutical and biotechnology customer goals (such as strategic leadership of clinical development plans, go/no go decisions, in-licensing, out-licensing, accelerated time to market, etc).
• Provide medical, clinical, scientific, regulatory, and product development leadership and consultancy expertise to support strategic business activities and investment opportunities.
• Participate in all aspects of Strategic Drug Development and lead the implementation of mission, goals and objectives, development of policies, procedures and standards for the department.
• Provide thought leadership in pharmaceutical product development by preparing publications, white papers, and blogs in areas of expertise and by participating in scientific conferences and webinars, as appropriate.
• Evaluate and develop product development strategies for pharmaceutical products (drugs, biologics, advanced therapies) focusing on clinical-commercial convergence that encompasses all phases of development from discovery to market, including preclinical strategy, clinical strategy, regulatory strategy, and commercial strategy.
• Support engagements with regulatory authorities (e.g., FDA, EMA) on behalf of customers, across the lifecycle of drug development from pre-clinical to licensing, including contribution to briefing documents and other meeting materials, and attendance and contribution to meetings and other interactions.
• Lead assessments of risk and probability of regulatory success and development of mitigations for candidate pharmaceutical products, including providing regulatory contributions to indication prioritization exercises, development strategy evaluations and gap analyses, due diligence, and similar activities.
• Support the innovative development of compounds to maximize technical, regulatory, and commercial success, including contribution to the development of Target Product Profiles (TPPs), Clinical Development Plans (CDPs), clinical study designs, synopses, and protocols, as appropriate.
• Strategic leadership of the development of regulatory submissions, including INDs, marketing/licensing authorizations (NDA/BLA/MAAs), special designations (orphan drugs, pediatrics plans, “fast-track”, “break-through” etc.…).
• Ensure high-quality, well-reasoned, objective deliverables (using data-driven design, where available and appropriate) that meet the highest standards of medical, ethical and scientific integrity and conduct.
• Assume the role of customer senior management as requested, including membership of virtual cross functional drug development teams.
• Provide drug development expertise to support strategic business activities and investment opportunities.
• Assist in the development of programs to maximize the organization’s growth and profitability.
• Ensure Customer Satisfaction by working closely with Senior Management, CRO Operations, Therapeutic Units, and other Operations Heads to ensure optimum strategic consultancy to customers.
• Serve as a key resource and participate in strategic business development activities including presentations to prospective clients, professional meetings or other business development activities for IQVIA Strategic Drug Development.
• Provide internal and external therapeutic and pharmaceutical development-related educational services in support of all branches of IQVIA business.
• Attend key scientific meetings/conferences and keep abreast of relevant scientific publications to maintain awareness of current scientific developments and progress in drug development methodology.
• Develop and maintain ongoing relationships with pharmaceutical and biotechnology companies, key opinion leaders identify new business opportunities.

Senior Director, Drug Development

Designer

• Responsible for study build & design, edit specifications, system configurations
• Collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives
• Design and update the eCRF using third party or in house CDMS tools
• Create and update Edit Specification Document
• Generate specifications for EDC build components
• Complete the Study Authorization Form and Trial Capacity Request Form (InForm)
• Attend project meetings and lead consultations as needed
• Communicate project risks to the Data Team Lead
• Ensure completion and documentation of all project-specific training
• Responsible for multiple study design projects
• Identify areas for process improvements on an ongoing basis.

Senior Clinical DB Designer

Data Scientist

• Independently manage end-to-end delivery of data management services for single/multi-service projects
• Provide comprehensive data management expertise to Clinical Data Management (CDM) team
• Serve as primary point of contact for customer on data management deliverables
• Lead direct negotiations with customer, e.g., timelines, financial, process, resources
• Continuously look for opportunities to improve service

Senior Data Team Lead – Veeva

Medical Billing and Coding

• Provide comprehensive data management expertise to the Data Management (DM) team to meet sponsor and company needs
• Perform Clinical Data Management and/or Coding activities
• May provide leadership as the Lead Coder or in a specific CDM task
• Manage delivery of coding activities through full study life-cycle
• Validates/tests the coding application and programming of coding reports
• Perform comprehensive data management and coding related tasks including conducting data review and writing and resolving data clarifications
• Manage coding related project timelines
• Perform Serious Adverse Event (SAE) reconciliation activities
• Handle audit requirements for respective studies including stand-alone coding projects as applicable
• Develop and maintain good communication and working relationship with the team

Clinical Data Coder

• Manage single and multi-service projects
• Provide expert skills as part of a Clinical Data Management (CDM) team
• Provide leadership to the team in the area of coding, project planning and execution
• Serve as an internal or external point of contact on standalone coding studies
• Manage the customer relationship for the project team

Senior Clinical Data Coder

Project Manager

• Validate the project scope, plans and schedules for moderately complex projects; adhere to metrics for project success and begin to suggest appropriate metrics.
• Manage day to day implementation of eCOA projects.
• Manage internal staff to support customer projects and manage internal service projects.
• Define and monitor project scope, budget, timelines, resources, quality and deliverables for the full project life cycle.
• Ensure the project team adheres to high quality service and all applicable corporate and client policies and standards.
• Regularly review project contract terms and conditions, and project plan to ensure that all assumptions are still valid.
• Work in close collaboration with the internal or external project stakeholders to achieve the study goals.
• Establish strong customer relationships and seek opportunities to increase customer satisfaction and deepen relationships.
• Communicate effectively with customers to identify needs and propose solutions.
• Keep customers well informed on status of internal service efforts and serve as liaison between internal staff and customers.
• Provide technical direction for the development, design, and systems integration for customer engagements.
• Responsible for managing the development, review and approval of project related study documentation during throughout the full life cycle of the project implementation.
• Provide regular updates and reports to Sponsor and IQVIA upper management.
• Conduct regular status meetings, reviewing project schedule, risks, issues and outstanding action items.
• Implement and monitor a risk management plan at the project level (raise to program level, as necessary).
• Implement corrective actions as needed to maintain project performance.
• Identify opportunities for improving and streamlining projects.
• Manage vendor relationship and tasks.
• Manage the Lessons Learned process throughout the project lifecycle.
• Communicate customer requirements to the product management teams, advocate on the customer’s behalf, and communicate the status of enhancement requests to customers.
• Manage project team members across multiple locations and time zones.

Project Manager, eCOA

Product Manager

• Lead product execution for AIMXR’s identity‑resolution and contextual intelligence capabilities
• Manage a team of Product Owners
• Translate strategic direction into prioritized outcomes
• Guide cross‑functional teams to deliver customer value at scale
• Define and track feature‑level KPIs
• Serve as a senior product point‑of‑contact for internal stakeholders and select client conversations
• Run lightweight experiments and A/B validations where applicable

Associate Director, Product Management

Strategy

• Own the vision, strategy, roadmap, and market success of IQVIA Digital’s flagship healthcare marketing platform
• Drive the transformation of Media OS into an intelligent, AI-powered audience and activation platform
• Establish strategic priorities and investment plans that support growth, innovation, and market leadership
• Lead the development of Media OS as an open, multi-platform ecosystem supporting diverse activation partners and media channels
• Champion customer success by delivering measurable improvements in reach, engagement, efficiency, and campaign performance

Product & Strategy Director

Human Resources

• Serve as primary HR Business Partner to Global BU leadership team members advising on organization design, workforce planning, talent, and culture
• Align HR strategy with global business priorities in partnership with the GCD Global HR Lead
• Use HR analytics and workforce insights to support data driven decisions
• Collaborate with global HR COEs (Talent Acquisition, Total Rewards, Leadership & Talent Development, HR Ops) to deploy scalable HR solutions
• Drive leadership development, succession planning, and employee engagement
• Lead reorganizations, M&A integrations, and workforce transitions
• Ensure adherence to local labor legislation while aligning with global standards
• Support leaders through change with clear communication and people first execution
• Oversee implementation of HR policies, compliance programs, and audit readiness
• Ensure timely HR reporting and insights to senior management
• Contribute to HR budgeting and identify opportunities to streamline HR processes
• Operate as a trusted advisor with strong influencing capability in a global, matrixed organization
• Collaborate with HR peers across R&D Solutions to ensure alignment of priorities and execution

Senior HR Director

Sales

• Strengthen key account relationships through customer visits and product demonstrations
• Collaborate with Territory Managers and Sales Management
• Drive utilization of targeted technologies across assigned accounts
• Manage expense and promotional budgets

Pharmaceutical Sales Associate – Urology

• Strengthen key account relationships through regular customer visits, product demonstrations, and educational programs
• Collaborate with Territory Managers and Sales Management to assess business conditions
• Drive utilization of targeted technologies across assigned accounts
• Prepare comprehensive account-level plans aligned with the Urology Division’s strategic goals

QA Engineer

• Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures.
• Prepare and distribute reports of findings to supervisor, operations staff, management, and customers.
• Provide consultation in interpretation of regulations, guidelines, policies, and procedures.
• Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.
• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions.
• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers.
• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures.
• Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans.
• Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned.
• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements.
• Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle.
• Lead/collaborate/support in QA initiatives/projects for quality, process improvements.
• Assist in training of new Quality Assurance staff.
• May be required to manage Quality Issues.
• May present educational programs and provide guidance to operational staff on compliance procedures.
• May perform pre-inspection visits at sites, host audits/inspections; ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections, as assigned.

Senior QA Auditor – GCP Audits

Research Analyst

• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
• Work with sites to adapt, drive, and track subject recruitment plan
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies by tracking regulatory submissions and approvals
• Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
• Create and maintain appropriate documentation regarding site management
• Collaborate and liaise with study team members for project execution support

Clinical Research Associate 2

Recruitment

• Coordinate the operational execution of patient recruitment and retention deliverables for assigned studies, ensuring alignment with the approved recruitment strategy and study timelines.
• Manage the coordination of translations, printing, and shipping of patient‑facing and study materials across multiple countries, working with internal teams and external vendors to ensure accuracy, quality, and timely delivery.
• Prepare and compile country‑specific submission packages and ensure required materials are delivered to Regulatory teams in accordance with submission requirements and timelines.
• Maintain and track study timelines, milestones, and deliverables using Smartsheet or other designated project management tools to support on‑time delivery.
• Support project‑specific, interdepartmental, and role‑specific training activities as required to enable consistent execution of recruitment processes.
• Maintain and manage large volumes of study‑related data, ensuring accurate and timely data entry into designated tracking systems and tools in accordance with project requirements.
• Support finance‑related activities, including contributing to periodic project and financial report generation and review.
• Ensure timely uploading, maintenance, and quality control of study documentation within eTMF/Wingspan or other designated systems, in compliance with company policies and regulatory standards.
• Ensure patient recruitment deliverables are completed accurately, compliantly, and within agreed timelines to support overall study execution.
• Identify operational risks, data discrepancies, or delivery challenges and proactively communicate issues and potential mitigation actions to relevant stakeholders.
• Perform additional duties as assigned by management to support overall project and departmental objectives.

Senior Medical Writer

Senior Director, Drug Development

Senior Clinical DB Designer

Senior Data Team Lead – Veeva

Clinical Data Coder

Senior Clinical Data Coder

Project Manager, eCOA

Associate Director, Product Management

Product & Strategy Director

Senior HR Director

Pharmaceutical Sales Associate – Urology

Pharmaceutical Sales Associate – Urology

Senior QA Auditor – GCP Audits

Clinical Research Associate 2

Patient Recruitment Specialist