IQVIA

Manager

• Project Leads are an integral part of clinical trial delivery, liaising with clinical teams.
• Responsible for project delivery of clinical studies to meet contractual requirements.
• Develop integrated study management plans with the core project team.
• Ensure the execution of clinical studies per contract, optimizing speed, quality, and cost.
• Set objectives for the core project team and/or sub-teams, communicate effectively.
• Monitor progress against the contract and present project information to stakeholders.
• Manage risks and contingencies proactively, leading problem-solving and resolution efforts.
• Ensure project quality by identifying risks and issues, responding to team concerns, and implementing corrective actions.
• Serve as the primary or backup project contact with customers.
• Build and lead the cross-functional project team, ensuring overall project delivery.

Local Trial Manager, Sponsor-dedicated

Bilingual

• Understand client requirements, project scope, and deliverables
• Lead project delivery and client meetings
• Manage vendor, Design & Delivery, and Data Processing
• Monitor and communicate deadlines to the team
• Check programmed questionnaires
• Ensure project profitability, timely delivery, invoicing, and collection
• Identify and develop work opportunities and client presentation

Engagement Manager – Public Health, French & English Bilingual

Research Analyst

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.
• Evaluate the quality and integrity of study site practices and manage the progress of assigned studies.

Clinical Research Associate II, Oncology

Events

• Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required
• Receive, triage, review and process Lifecycle safety operational data
• Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations
• Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data
• Build a positive, collaborative team environment with Lifecycle safety team members, lead by example
• Establish and maintain effective team project service operations communications
• Liaise with Project Manager by proactively identifying issues and proposing solutions
• Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives

Medical Information and Adverse Event Intake Specialist, Slovenian, Croatian, English

Project Manager

• Supervise and manage an assigned team of CPC/ PMA and their subsidiaries.
• Ensure project milestones are met.
• Ensure compliance with standard processes, policies and procedures.
• Train and onboard new-hired Project Management Analysts.
• Complete and discuss PMA competency framework with each direct report.
• Actively engaged with the review of project performance dashboard.
• Review and track employee resource allocation.
• Produce status and tracking reports for team members and senior management.
• Ensure direct reports process and approve invoices.

Project Manager – Instrument Licensing

• Provide phone support to health care professionals and consumers regarding adverse events, product quality complaints, medical inquiries, product support, and other needs as required
• Receive, triage, review and process Lifecycle safety operational data
• Perform data entry for tracking and Lifecycle safety databases, coding relevant medical terminology, writing descriptive narratives, generating queries pertinent to the case, performing quality control, assisting with reconciliation, driving case closure, coordinating translations
• Receive and document incoming telephone calls or emails from investigative sites or other sources reporting safety data
• Build a positive, collaborative team environment with Lifecycle safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff
• Establish and maintain effective team project service operations communications
• Liaise with Project Manager by proactively identifying issues and proposing solutions
• Participate in training across Lifecycle safety process service offerings, participate in working groups as applicable in implementation of new initiatives

Medical Information and Adverse Event Intake Specialist, Lithuanian, English, Foreign Language

Field Engineer

• Installer et mettre à jour des dispositifs médicaux
• Effectuer une maintenance préventive
• Fournir un soutien à la clientèle aux hôpitaux
• Documenter et soumettre des données quotidiennes

Field Service Technician, Bilingual (French/English)

Supply Chain

• Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution
• Create master English label text in accordance with relevant regulatory framework
• Create and maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in accordance with the project requirements
• Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery
• Setup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed
• Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it
• Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations
• Remain up to date in all GxP and regulatory requirements applicable to the role
• Leads client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates
• Creates a Temperature Excursion management plan
• Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed

Clinical Supply Chain Manager

Financial Planning and Analysis

• Lead and manage the full scope of assigned project(s)
• Serve as primary point of contact for stakeholders
• Develop, maintain, and oversee comprehensive project plans
• Review and manage project budgets and scopes of work
• Ensure project data and metrics are accurately maintained
• Provide direction to project team members
• Identify, assess, and manage project risks
• Drive continuous improvement initiatives

Associate Director – PSCS Finance Operations

Business Development Rep

• Prospect accounts focusing on Safety and Regulatory products and services
• Identify and develop new accounts and follow up on existing leads
• Develop and maintain productive relationships with key target accounts
• Manage assigned accounts to generate both incremental and repeatable annual business
• Initiate and manage RFI and RFP process and negotiate terms for all account programs and projects
• Work collaboratively with the Professional Services Organization to ensure a complete and professional delivery of software and service solutions
• Expand sale of product portfolio in the Safety and Regulatory market
• Collaborate with Executives and SMEs to maximize account coverage
• Maintain knowledgeable understanding of changing regulatory guidelines and mandates affecting the industry community

Associate Business Development Director – Safety Solutions

Client Services Representative

• Responsible for overall management of assigned projects on specific accounts including coordination of digital and interactive content, working with content experts to validate scientific accuracy, achieving project goals, and timelines
• Prepare and deliver client presentations in a manner that effectively showcases the featured content as directed by client, internal departments, and Key Opinion Leaders (KOLs)
• Drive long-term planning of assigned accounts including timelines, quality assurance, SOP creation and adherence, and budget monitoring
• Monitor project to guarantee adherence and pull-through of client strategy
• Supervise and train junior staff members, as applicable, by creating a positive work environment, fostering a team approach, manage training and development, and oversee project progress
• Manage and attend relevant internal meetings, as assigned
• Contribute to enhanced customer service through timeliness and quality of communications and deliverables, including thorough hand-offs to internal project teams
• Adhere to all standard operating procedures (SOP’s) and drive internal project team adherence to PIT Crew, Basecamp, CCR, Good to Go, and Weekly client update meetings SOPs
• Develop and maintain working knowledge of managed products and disease areas
• Develop and assist with preparation of client pitches, presentations, and metrics
• Manage faculty recruitment, engagement, and relationships on behalf of clients
• Maintain regular contact with client to ensure expectations are met
• Plan, schedule, organize team members, and prepare client update agendas and summaries to facilitate and lead client update meetings
• Synthesize client feedback for implementation by project team members
• Collaborate with internal project team members and departments including Scientific Services, Interactive/Graphics, and Marketing to ensure client expectations are being met
• Track and report on all opportunities, key milestones, support requirements, etc.
• Establish meaningful, professional relationships with various client stakeholders, including gaining understanding of their individual roles, communication preferences, personal motivators, and the desired outcomes for the brand and for the team
• Ensure Simpson’s brand is properly represented and promoted throughout client interactions, communications, and deliverables
• Promote and deliver service levels which are sustainable and allow for efficient delivery of a quality product
• Provide data, decisions and delivery of services in support of client, project and community success

Client Service Director – Marketing, Brand Promotion

Operations

• Lead the review of ATS pricing methodologies and strategies across the full portfolio
• Design, build, maintain, and continuously enhance pricing calculators for key ATS products
• Propose and implement improvements to simplify, standardize, and harmonize pricing approaches and tools
• Provide pricing governance, ensuring consistency, transparency, and adherence to established frameworks
• Develop a strong understanding of cost structures and margin drivers for ATS offerings
• Apply financial and analytical rigor to assess pricing viability, discounts, and profitability
• Partner with Sales to support strategic deal reviews , discounting processes, and approvals
• Act as a trusted advisor to commercial and sales leadership on complex pricing topics
• Lead the definition of business requirements for pricing automation initiatives
• Communicate clearly and confidently with senior stakeholders

Senior Manager, Commercial Operations, Pricing

Sales

• Support projects related to Commercial Analytics SFE, including Segmentation, Targeting, Sizing, and Alignment
• Experience in Patient Analytics is a strong plus
• Assist in reviewing and analyzing client requirements to support proposal development and client‑focused solutions
• Contribute to the creation of detailed project documentation, technical specifications, and analytical frameworks
• Perform quantitative and qualitative analyses to identify client issues and support solution development
• Assist in designing and structuring presentations tailored to the target audience
• Develop and present clear, structured client deliverables within established methodologies
• Proactively develop foundational knowledge of consulting methodologies, analytics frameworks, and the life sciences marketplace
• Work under the guidance of Senior Consultants, Engagement Managers, or Principals on assigned project responsibilities
• Collaborate effectively across cross‑functional teams to achieve engagement objectives

Salesforce Effectiveness Consultant

• Adopt and implement the global Quality Management Plan within the scope of the assignment
• Cooperate closely with the relevant business and other stakeholders
• Provide advice and support to teams on all aspects of Good Clinical Practice (GCP) compliance
• Work closely with Quality Assurance and assigned business staff in case of suspected misconduct

Quality Manager

Clinical Operations

• Provides input to the overall operational trial(s) implementation, manages trial(s) timelines, budget, feasibility, country identification and sites selection, enhanced patient recruitment, and functions as the primary liaison for internal stakeholders and vendors.
• Accountable to deliver Trial(s) on time, within budget, and with highest achievable quality.
• Assist in the review, development and/or writing of clinical trial documents and manuals, including but not limited to Protocol, Case Report Forms, informed consent forms, Clinical Study Report and other regulatory documents.
• Lead the evaluation and selection of investigative sites; responsible for feasibility.
• Select, coordinate and monitor activities of vendors Review of monitoring reports and conduct co-monitoring visits, as needed.
• Develop and manage trial(s) timelines, budget and priorities.
• Participate in data review and discrepancy resolution.
• Ensure set up and maintain all systems in order to plan and implement trial(s) and track progress.
• Generate reports to update management on conduct of trial.
• Ensure appropriate clinical trial supply plans are implemented and managed.
• Develop recruitment plans, risk-mitigation plan, monitor, and implement contingencies as required.
• Participate in monitoring study safety.
• Review key study quality metrics (e.g., eligibility, primary endpoint data, etc.) and determine appropriate action in conjunction with study team.
• Perform initial review of CRO and other third party study vendor invoices to ensure that work is performed in accordance with scope of work.
• Assist with CRA and third party vendor training on protocols and practices.
• Lead the multi-disciplinary trials teams; include the study team meetings.
• Function as the primary contact for trial(s) between Drug Development and other departments.
• Assume responsibility to participate as a member of working groups and perform special projects, as assigned.
• Ensure adherence to Good Clinical Practice and all applicable local and international regulations.