IQVIA

Affiliate Manager

• Develop and deliver insightful commercialization strategies for EBP clients
• Conduct strategy sessions with clients to outline integrated commercial launch plans
• Lead senior/executive level meetings to support launch planning
• Create and elevate new business opportunities through identification of follow-on work

Asset Commercialization Partner – Emerging Biopharma

Manager

• Manage or lead multiple consulting projects ensuring on-time and on-budget delivery for clients.
• Serve as key point of contact with IQVIA clients, mainly pharmaceutical and biotechnology companies.
• Manage project teams in the design, development, and delivery of client deliverables.
• Provide direction, advice, and intellectual leadership to clients and delivery teams.
• Leverage experience to identify strategic alternatives and approaches to client questions.
• Provide follow-up with clients after project delivery to ensure satisfaction.
• Support the development of intellectual property for use on future engagements.
• Ensure the development and delivery of client reports and presentations.
• Share subject matter expertise with others to enhance capabilities.

Manager, Advisory Services

Data Analyst

• Review and verify that all delivered files meet specified order requirements and client expectations.
• Perform detailed quality control checks on file contents, ensuring accuracy, completeness, and compliance with data governance standards.
• Document and report any issues, discrepancies, or failures in file delivery to relevant stakeholders promptly.
• Collaborate with internal teams (Delivery, Data Management, Product, and Governance) and external vendors to resolve QC issues efficiently.
• Maintain accurate records of QC checks, issue logs, and resolutions for audit and continuous improvement purposes.
• Prepare and present QC reports and summaries for internal and client review.
• Identify recurring issues or process gaps and propose solutions to enhance data quality and delivery reliability.
• Support onboarding of new data sources by validating test/sample files and ensuring they meet QC standards before release.
• Meet service level agreements (SLAs) for QC response times and issue resolution.

Data Quality & Analytics Manager

• Responsible for the on-time completion of projects or components of complex projects for clients in the pharmaceutical market access consulting space
• Identifies and elevates potential new business opportunities
• Plans, organizes, and manages resources to bring about the successful completion of specific project goals and objectives
• Executes high quality research and analysis
• Designs, structures, and delivers client reports and presentations
• Develops client relationships through face-to-face discussions or workshops, telephone or email contact
• Identifies opportunities for follow-on work and new leads
• Supports the development of intellectual property for use on future engagements
• Supports development of proposals
• Develops broader and deeper knowledge of consulting methodologies and pharmaceutical market through on-the-job experience and training
• Coaches project team members and supporting them to fulfill their personal objectives
• Coaches junior staff (not just in projects)
• Leads some learning, development, and recruiting activities.

Manager, Value & Access Strategy Consulting

Software Engineer

• Good Experience in Tibco Spotfire Professional, Web player and analytics server for loading data from databases, creating visualization and filters.
• Hands on knowledge in assisting users in creating, modifying Spotfire visualization dashboard and getting data into Spotfire from different data source
• Ability to independently design, visualize and implement a solution.
• Should be able to translate specifications into Tibco Spotfire Visualizations. Independently communicate with customers to understand requirements
• Ability to develop the dashboard by using scripts (Iron python, HTML etc.) and good experience in using Data canvas.
• Strong expertise in Database (SQL, Oracle, PLSQL and etc.).
• Good knowledge in Microsoft Excel.
• Creating information models, procedures, Information links, Data functions and Data Connections.
• Strong knowledge on Property Controls, Script Controls and Document properties
• Performance Optimization.
• Trouble shooting and bug fixes.
• Strong Clinical knowledge - RAVE.
• Good Inter-personal skills.
• Good analytical and Problem-solving skills.
• Excellent written and verbal communication skills. Ability to work effectively in a team as well as individually.
• Ability to interact with corporate team and CDM team members to negotiate timelines, responsibilities, and deliverables.

Spotfire Programmer

Recruitment

• Collaborate with pre and post award stakeholders to manage the coordination, planning, and implementation of Patient Recruitment and Retention support operational plans on larger, multi-region studies or programs
• Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan
• Make proactive operational and tactical recommendations as needed based on study performance
• Collaborate with internal teams and external providers to deliver all appropriate tactics associated with the recruitment/retention strategy
• Represent IQVIAs Patient Recruitment at site/sponsor-facing meetings to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required
• Ownership for study KPI and financial performance
• Act as senior oversight for large studies/programs leading a team and taking overall ownership for study performance
• Develop plans to ensure the allocation of human, material, system and fiscal resources for assigned area of accountability

Patient Recruitment Delivery Lead

Research Analyst

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• Collaborating with experts at study sites and with client representatives

Senior Clinical Research Associate

• Perform monitoring and site management work
• Conduct site monitoring visits in accordance with regulatory requirements
• Manage the progress of assigned studies by tracking submissions and approvals
• Ensure site documents are available for filing
• Collaborate and liaise with study team members

Clinical Research Associate, Sponsor Dedicated

Call Center Representative

• Provide initial support for customer requests via telephone, email, fax, or other available means of contact to the Support Center
• Quickly assess the user's issue and provides first level support for problem resolution
• Document information specific to the resolution and escalate unresolved issues expeditiously to the appropriate area
• Recognize operational challenges and suggest recommendations to management, as necessary
• Ability to work 40 hours per week (shifts available: 8:00 am - 5:00 pm EST or, 9:00 am – 6:00 pm EST or, 10:00 am - 7:00 pm ET or, 11:00 am EST – 8:00pm EST) under moderate supervision

Pharmacy Tech Support – Call Center Rep

• Provide initial support for customer requests via telephone, email, fax, or other available means of contact to the Support Center
• Quickly assess the user's issue and provides first level support for problem resolution
• Document information specific to the resolution and escalate unresolved issues expeditiously to the appropriate area
• Recognize operational challenges and suggest recommendations to management, as necessary
• Ability to work 40 hours per week under moderate supervision
• Multiple shifts available: 8:00 am - 5:00 pm EST, 9:00 am – 6:00 pm EST, 10:00am – 7:00pm EST, 11:00 am – 8:00pm EST

Bi-lingual Pharmacy Tech Support/Call Center Rep

• Provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs.
• Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs.
• Provide technical expertise and leadership to the department.
• Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
• Perform, plan and co-ordinate the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries.
• Program and plan the integration of databases from multiple studies or sources.
• Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
• Provide advanced technical expertise in conjunction with internal and external clients.
• Fulfill project responsibilities at the level of statistical team lead for single complex studies or group of studies.
• Manage project budget and resource requirements, and provide revenue forecasts for single studies.
• Provide training and guidance to lower level staff.

Senior Statistical Programmer

Clinical Research

• Review of scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability.
• Evaluation the quality of assessments, conducting live interactions with raters to discuss assessment methodology, scoring technique, and to provide guidance, as necessary.
• Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).
• Complete rater interactions and assigned tasks as scheduled.
• Responsible for timely submission of all documentation associated with assigned tasks.
• Participate in all orientation, training and calibration activities as required.
• Functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.
• Contacting clinical trial participants remotely (e.g., via proprietary app, Engage) to administer assessments, and will appropriately document resultant information (e.g., notes, scores)

Clinical Scientist, Clinical Science

• Manage a team of Statistical Programming (SP) staff, including hiring, training, and supervising department members.
• Develop, recommend, and implement standard procedures, measures of performance, and training programs.
• Organize and allocate resources according to multi-project requirements and deadlines.
• Serve as lead statistical programmer on projects.
• Technical responsibilities: i) Serve as a Stat Programming consultant for other members of the department and staff members from other Biostatistics departments within the company. ii) Maintain knowledge and awareness of developments in statistical programming. iii) May participate as high level lead Stat Programmer on major project(s). iv) Provide advanced technical expertise for internal and external clients. v) Independently bring project solutions to SP teams and the Statistical Programming department. vi) Provide expert review of process and methodology development work with regard to SP standards and validation procedures.
• Hold at least bi-monthly meetings with direct reports to discuss, at a minimum: project status, including timelines, delivery updates, financial aspects of the group or project, and potential risks, associated mitigation and support required; status of any initiatives that they may be involved in; the team's utilization rates; the direct report's training and other administrative obligations, such as Standard Operating Procedures (SOPs) and corporate training mandates; personnel issues; and career or training objectives.
• Develop and implement plans for measuring and improving employee engagement, ensuring global consistency.
• Collaborate with project leads to address work scheduling for current and projected projects, staffing needs, technological needs, and projected peak workloads, ensuring global consistency, where possible. Develop and manage associated action plans to hold members accountable.
• Efficiently conveying messages from leadership to direct reports and teams, as well as effectively communicating issues and opportunities up to leadership.
• Might be needed to serve as the designated substitute or alternatively ensure coverage is in place for direct reports during their absence or in case of turnover.
• Attend and participate in Bid Defenses, Kick off Meetings (KOM), as applicable. Support Request for Information (RFI), Request for Pricing (RFP), and budgets, as requested.
• Participate / Support internal and external audits and inspections, as required. Also ensure required staff is assigned, trained and prepared to support.

Manager, Statistical Programming

Engineer

• Collaborate with cross-functional teams to support the deployment and maintenance of applications
• Participate in on-call rotations to support 24/7 operations
• Manage and optimize system performance and reliability
• Identify and troubleshoot technical issues in a timely manner

DevOps Engineer

Business Analyst

• 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 data to the client
• 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
• Support in preparation of project plans
• 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
• Act as a backup for colleagues, based on business requirements