IQVIA

Medical Director

• Provide strategic leadership and scientific direction across client accounts, therapeutic areas, and organizational initiatives.
• Lead, mentor, and develop Medical Directors, Scientific Directors, and medical writers, fostering a culture of excellence, accountability, and professional growth.
• Serve as a senior scientific advisor to clients, building trusted partnerships and shaping medical communication strategies that address evolving business and stakeholder needs.
• Maintain accountability for the scientific quality, accuracy, and strategic integrity of client deliverables across the portfolio.
• Oversee complex and high-impact initiatives, including product launches, advisory boards, speaker development programs, congress activities, publications, medical education, and strategic planning engagements.
• Partner with cross-functional leaders across account management, engagement strategy, project management, editorial, and creative teams to ensure seamless execution and successful delivery of client programs.
• Drive operational excellence by identifying risks, removing barriers, and ensuring effective allocation of scientific resources across projects and accounts.
• Contribute to business growth through strategic planning, proposal development, client relationship expansion, and new business opportunities.
• Provide leadership during project challenges, stepping in as needed to guide teams and ensure successful outcomes.
• Support talent acquisition, onboarding, succession planning, and workforce development initiatives.
• Represent ENOVA and IQVIA at key client meetings, advisory boards, congresses, and other external engagements.

Medical Director – Medical & Scientific Communications

Data Scientist

• Drive offering development and delivery excellence using AI
• Lead business development efforts including solution shaping and proposal development
• Collaborate with Technology Client Partners to sell solutions across technology, data, and analytics products
• Shape the vision and roadmap for the Technology & AI practice
• Collaborate with internal offerings teams to build and enhance offerings
• Architect scalable AI and data solutions aligned with client business goals
• Ensure engagements meet technical, financial, and quality standards

EBP Analytics Technology Lead

General

• Lead end-to-end country-level trial management, from study start-up through database lock and closeout
• Serve as the primary contact for assigned clinical trials within your country
• Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
• Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target
• Partner with CRA’s, Global Project Leads, and cross-functional teams to ensure successful study execution
• Lead site feasibility, selection, and activation processes
• Drive investigator engagement and site performance, including recruitment and retention strategies
• Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
• Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
• Oversee patient safety reporting (AEs/SAEs) within required timelines
• Manage country-level budgets, forecasting, and financial tracking
• Oversee local vendors and site payments, ensuring timely and accurate processing
• Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
• Ensure compliance with local regulations and global standards (ICH-GCP)

Clinical Project Lead, Oncology

• Provide medical expertise on pharmacovigilance services to divisions as requested.
• Participate in all aspects of Medical Safety’s involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.
• Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary.
• Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements.
• Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported.
• Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile.
• Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data.
• Represent safety and clinical data review findings during client meetings.
• Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports.
• Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies.
• Provide medical oversight for label development, review and change.
• Provide medical support and attendance at Data Safety Monitoring Board Meetings.
• Attend and contribute medical safety evaluation on Safety Monitoring Committees.
• Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document.
• Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments.
• Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract.
• Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture.
• Act as Global Safety Physician or Assistant or Back-up on projects as assigned.
• Attend project meetings, medical safety team meetings, and client meetings as requested.
• Ensure coverage for all medical safety deliverables within regulatory or contracted timelines.
• Provide medical escalation support for medical information projects.
• Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects.

Associate Medical Safety Director

QA Engineer

• Evaluate patient services interactions using approved Quality Monitoring frameworks
• Apply quality standards consistently and document clear, defensible scoring rationales
• Identify and escalate compliance risks
• Support monthly quality trend reporting
• Maintain accurate documentation to support audit readiness

Quality Assurance Business Analyst – Patient Access & Support Services

Nurse Educator

• Facilitate connections between patients and approved educational resources.
• Deliver direct, disease-specific education and training related to prescribed medications.
• Support multiple disease states and therapies as needed.
• Promote behavioral change through patient-centered education to improve treatment adherence.
• Encourage effective communication between patients and their healthcare providers.

Field Nurse Educator

Director

• Responsible for direct oversight of Ambassador Regional Project Leads and their teams and of IQVIA Ambassador Project Training team
• Communicate with client Ambassador Director on a regular and timely basis
• Ensure that IQVIA Force have the appropriate resources and operational support required to deliver on both patient and client expectations
• Develop and implement a robust plan to facilitate clear communication to client’s Ambassador organization
• Attend and jointly lead weekly program staff meetings in conjunction with the client leadership team
• Identify opportunities and participate in the development of operational strategies, tactics and resources required to drive performance and optimize value for patients
• Collaborate with client and IQVIA Senior Leadership to support KPI development
• Provide Senior Leadership with updates on policy developments and likely impact to patients and service delivery
• Provide patient support activities as directed for other client programs and initiatives

Senior Project Lead – Field Director

Product Manager

• Support the development of the product road map and new features
• Work with stakeholders to support roadmap development
• Develop strong relationships with stakeholders and engineers
• Understand market and customer requirements and translate them into features

Per Diem

• Deliver in-home clinical services to patients initiating therapy with complex medications.
• Perform in-home blood specimen collection, labeling, and transporting specimens according to network policies, procedures, and regulatory standards.
• Comply with all laboratory safety and handling procedures; ensure appropriate delivery to designated laboratories.
• Conduct screenings such as electrocardiograms (EKGs) and macular edema screening exams (training provided).
• Maintain a clean and organized work environment, including transportation and supplies storage specific to the In-Home Network.
• Monitor and manage clinical supply inventory.
• Collaborate with IQVIA’s clinical coordination team to execute and submit appropriate visit-related paperwork promptly and accurately.
• Identify and report adverse events, medical product complaints, or patient inquiries in accordance with IQVIA and manufacturer guidance.
• Maintain accurate mileage and time logs for reimbursement and compliance purposes.

Mobile LVN/LPN – Per Diem In-Home Services

Medical Assistant

• Perform in-home blood specimen collection, labeling, and transporting specimens
• Conduct screenings including electrocardiograms (EKGs) and macular edema screening exams
• Collaborate with clinical coordination team to submit visit-related paperwork

Mobile Medical Assistant, Phlebotomist – Per Diem In-Home Services

Associate

• Lead implementation of evidence synthesis projects to support HTA and/or regulatory submissions from pre-award to final delivery
• Lead project teams to ensure the execution of rigorous and high quality deliverables according to timelines
• Expert ability to synthesize data qualitatively and quantitatively, and guide junior staff
• Manage projects, oversee the operational, financial, and administrative requirements of projects
• Independently qualify leads, develop proposals, attend bid defenses, and manage the contracting process
• Support more senior staff on specific business initiatives as required
• Work effectively across time zones as part of a global team

Associate Principal, Indirect Treatment Comparison, Evidence Synthesis

Account Manager

• Promote a product to specialty healthcare providers in an assigned territory.
• Collaborate with clients to deliver on commitment to serve patients.

Key Account Representative

Consultant

• Acquire and demonstrate a working knowledge of our products/therapies and develop an understanding of their applications.
• Improve patient outcomes by delivering ventricular medical device education in a variety of settings, including but not limited to, the ICU, OR, and Cath Lab.
• Ventricular medical device case support, including on call support.
• Complete proactive rounds for patients receiving support and provide assistance.
• Collaborate with the Clinical Support Center (CSC) for ongoing additional support as necessary.
• Maintain clinical competency in current product line, patient management, and remain up to date on most relevant information through continual learning and education.
• Some travel may be needed.

Part Time Clinical Nurse Consultant

Research Coordinator

• Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
• Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
• Be part of a supportive team that values initiative, adaptability, and continuous learning.
• Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.

Senior Research Coordinator

Data Management

• Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction.
• Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs.
• Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables.
• Gather Study Set up requirements through discussion and communication with relevant stakeholders.
• With Minimal guidance - support, overview of validation of new Device integrations.
• Oversight & Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
• Ensure that all the deliverables are of expected quality standards and meet customer expectations.
• With guidance, ensure service and quality meet agreed upon timelines and deliverables in contract/Scope of Work (SOW).
• Support Training of New joiners.
• Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
• Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended as required.
• With Guidance manage & oversight the implementation of new technology / database revisions.
• Work closely with the programming team for process innovation and automation.
• Be compliant to trainings and eSOP reading.
• Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
• Communication with Line Manager, and other team members across functions should be collaborative.