Lifelancer

Paralegal

• Manage worldwide trademark filings, including prosecution, maintenance, renewals, and communication with business stakeholders
• Prepare and file trademark applications, Madrid Protocol applications, and other trademark prosecution documents
• Communicate with foreign associates regarding trademark prosecution, maintenance, enforcement, opposition, and cancellation proceedings
• Review and analyze trademark watch notices and recommend potential enforcement actions
• Coordinate responses to office actions, oppositions, cancellation proceedings, and other trademark disputes
• Prepare and review affidavits, declarations, powers of attorney, assignments, and related trademark documentation
• Assist attorneys with intellectual property due diligence, mergers and acquisitions, divestitures, and other transactional matters
• Support domain name portfolio management and enforcement, including registrations, renewals, transfers, monitoring, UDRP proceedings, and online trademark enforcement
• Collaborate with outside vendors on global customs recordation and brand protection initiatives
• Maintain and renew U.S. Customs trademark recordations
• Maintain accurate trademark records and docket deadlines in Amgen’s trademark management system
• Serve as a key liaison among attorneys, business clients, foreign counsel, and external service providers
• Support Amgen’s in-house Trademark, Copyright and Brand Protection Team in protecting and strengthening its global biotechnology brand

Senior Associate Paralegal – Trademark

Medical Director

• Provide medical direction for the conduct of clinical trials
• Support development activities for proposed and ongoing projects within the area of expertise
• Perform medical monitoring for assigned clinical studies
• Partner with GCO to develop and enhance client relationships
• Provide medical/scientific capabilities to clients, proposal teams, and internal teams
• Drive projects from an overall company perspective beyond the medical perspective
• Provide strategic and tactical subject matter expertise for proposals, bid defense, business development, quality/process improvement, and audits
• Contribute to company policies involving medical, safety, and therapeutics
• Provide cross-functional scientific and technical contributions to client medical teams, project teams, investigators, sites, regulatory authorities, ethics committees, safety monitoring boards, and healthcare professionals
• Perform site/investigator feasibility and build investigator relationships to support trial recruitment and conduct
• Participate in client and internal meetings across time zones
• Support recruitment for department positions
• Lead and present medical/scientific capabilities in proposal teams
• Manage, supervise, and delegate activities to up to 5–10 direct and indirect reports as applicable
• Serve as Global, Regional, or Program Lead Project Physician across multiple indications as assigned
• Contribute to medical strategy and study/program execution
• Review and revise protocols, case report forms, training materials, project tools, analysis plans, clinical trial reports, data tables, listings, figures, and new drug applications
• Prepare materials for and participate in investigator meetings and assist at site initiation visits
• Participate in project risk assessment activities
• Provide out-of-hours medical cover as required
• Perform medical data review and oversee central medical data reviewers where applicable
• Review and act on safety alerts
• Support medical review of coding
• Assist with data safety monitoring board activities
• Provide clinical and medical expertise to other company departments
• Review or assist with medical monitoring scope of work, hours, and budget discussions
• Oversee medical monitoring activities, timelines, quality of deliverables, and physician resource assignments
• Maintain subject matter expertise through CME, clinical work, and relevant conferences/meetings
• Develop training modules and provide disease-area and protocol-specific training
• Participate in company-wide process improvement activities
• Represent the company at conferences and scientific meetings
• Lead therapeutic-area physician initiatives
• Perform other duties as assigned

Senior Medical Director – MD

General

• Educate health care providers on patient support programs, access, and reimbursement using AbbVie-approved tools and services
• Serve as a subject matter expert on local, regional, and national payer policies and requirements
• Develop and sustain relationships with relevant providers within the territory
• Exchange clear, concise, and efficient information with Field Reimbursement Managers, HCPs, and other stakeholders
• Collaborate across sales, market access, and patient services teams to update HCPs on prescription status and program eligibility
• Use approved resources and data to support HCP education initiatives and enhance patient experience
• Identify and report payer trends for approved products to Patient Services and market access account management teams
• Own process-improvement initiatives to enhance system efficiency and patient access strategies

Virtual Access Specialist

Sales

• Provide outbound marketing, disease-state identification and education, and inbound customer support in a virtual pharmaceutical environment
• Deliver proficient sales presentations to current and prospective customers
• Plan and organize activities for regular and consistent territory coverage
• Execute client-directed outbound calls, emails, and virtual strategic interactions
• Develop daily and weekly call schedules for efficient coverage of assigned targets
• Maintain accurate records of calls, emails, and appointments in the CRM system
• Clearly articulate clinical benefits and product value to healthcare professionals and office staff
• Use educational resources and support materials in customer interactions
• Foster trust and credibility through consistent, professional virtual communication
• Administer territory information and comply with reporting and regulatory requirements
• Complete assigned company and job-related training

Virtual Pharmaceutical Sales Specialist

Project Manager

• Serve as Project Lead and primary sponsor contact
• Accountable for overall project delivery, including quality, time, and cost
• Establish and communicate customer expectations to the project team
• Ensure internal and external escalation pathways are followed
• Delineate responsibilities and communication pathways for secondary project leads when required
• Lead cross-functional project teams to meet or exceed deliverables
• Maintain financial stewardship, including contract understanding, resource alignment, out-of-scope activity management, Con Mod negotiations, and timeline execution
• Drive risk identification and issue resolution at project level through RBQM/RESOLVE
• Ensure project team compliance with organizational policies, SOPs, ICH-GCP, regulatory, and project-specific requirements

Senior Project Manager – Neurosciences, Psychiatry or Rare Diseases Team

Contracts Specialist

• Act as a Subject Matter Expert on Clinical Trial Agreement processes at country and site level
• Prepare, negotiate, and finalize site contracts and budgets
• Manage the Investigator Budget
• Act as a key liaison for contract-related communications
• Resolve negotiation issues and escalate risks
• Drive process improvements
• Contribute to SOP development and keep templates updated
• Liaise and collaborate with Worldwide stakeholders and external stakeholders, including sites and investigators
• Review and finalize Clinical Trial Agreements and associated documents, including site budgets, for completeness and accuracy

Principal Specialist, Site Contracts

Auditor

• Execute the Clinical audit program, including scheduling, planning, reporting, and resolution of Clinical audits
• Ensure alignment with RDQA policies and procedures
• Contribute to development and implementation of the Clinical QA quality system
• Provide advice and support on GCP and quality topics to business partners
• Evaluate Clinical processes through audits and QA oversight activities to assure quality and compliance
• Lead and participate in Clinical Audit scheduling, planning, and conduct activities
• Conduct investigator clinical site, process, system, and Affiliate audits
• Communicate audit results orally and in writing within target timeframes
• Review and approve Corrective Action Plans and track actions to completion
• Contribute to development and implementation of systems and processes supporting global quality assurance requirements
• Support maintenance or development of Quality standards relating to Clinical audit
• Contribute to continuous improvement initiatives and projects
• Participate in and support GCP inspections as required
• Provide GCP regulatory support and consultation to RDQA and business partners
• Promote continuous education on quality, clinical guidelines, and regulations

Auditor, RDQA Clinical Quality Audit

Customer Success Manager

• Develop and execute the Customer Success multi-year plan for the Resins & Technologies portfolio
• Establish a unified customer engagement model across insights, analytics, adoption, technical partnership, and commercial governance
• Elevate Voice of Customer capabilities and integrate customer insight into product, R&D, and commercial strategy discussions
• Own and lead the Resins and Technologies Go-to-Market strategy
• Lead Go-to-Market planning, positioning, segmentation, and customer adoption pathways
• Enable global Sales, Marketing, and R&D teams through Commercial Playbooks and data-driven targeting
• Drive portfolio growth through analytics, competitive intelligence, and customer-focused value differentiation
• Lead and develop the Customer Success organization
• Directly manage leaders responsible for Customer Success & Adoption, Customer Insights & Product Analytics, and Spec-in Governance
• Provide senior oversight for Go-to-Market implementation and growth initiatives with the global commercial organization
• Coordinate customer programs for Cytiva’s new manufacturing site in Muskegon, Michigan, USA
• Provide business unit guidance for contracts and negotiations
• Set the vision for customer, product, and market analytics
• Oversee segmentation, customer journey mapping, adoption analytics, and whitespace identification
• Integrate predictive analytics and customer health metrics into lifecycle management
• Govern and continuously improve the end-to-end customer journey
• Drive onboarding, adoption, retention, satisfaction, and long-term partnership initiatives
• Build scalable processes for proactive customer engagement, escalation management, and systemic issue resolution
• Report to the VP for Product Management in the Resins and Technologies business unit

Senior Director, Customer Success – Resins and Technologies

Consultant

• Review services for medical necessity and appropriate benefit use
• Facilitate efficient discharge planning
• Collaborate with providers and facilities to support members with complex needs
• Assess, plan, implement, coordinate, monitor, and evaluate healthcare services and benefits
• Collect and evaluate clinical information
• Apply clinical criteria, guidelines, policies, and judgment to make coverage determinations
• Communicate with providers and external partners to coordinate care and treatment plans
• Identify opportunities for referrals to additional programs, services, or care solutions
• Promote quality care delivery and effective benefit utilization
• Serve as a resource to internal and external stakeholders regarding utilization management processes and clinical considerations
• Coordinate, document, and communicate all aspects of the utilization and benefit management process
• Ensure members receive appropriate care while meeting state and federal requirements and turnaround times

Utilization Management Nurse Consultant

Medical Scribe

• Support primary care providers with clinical documentation so they can focus on patient care
• Huddle each morning to plan the day's visits
• Join providers in exam rooms to observe and document patient visits
• Document patient encounters in structured notes, including history of present illness, assessment, plan, and physical exam
• Assign appropriate CPT and ICD-10 codes
• Prepare After Visit Summaries
• Consult with providers to ensure accurate and specific documentation
• Request and review medical records
• Use population health tools to support clinical documentation improvement
• Prepare for and support Daily Huddles and Clinical Documentation Reviews
• Consult with providers on clinical documentation opportunities
• Place orders and referrals
• Address tasks and provide additional administrative support to the care team
• Perform other duties as assigned

Marketing

• Support the HCP Lead in translating brand strategy, customer insights, thought leader perspectives, and field input into peer-to-peer priorities, engagement plans, and execution roadmaps
• Develop and quarterback the TAVNEOS peer-to-peer engagement strategy
• Lead assigned peer-to-peer initiatives from strategy through execution
• Lead cross-functional workstreams across Brand, TLLs, Sales, Medical Affairs, Marketing Operations, agencies, and enterprise partners
• Build compliant relationships with speakers, faculty, and influential HCP stakeholders
• Identify, engage, onboard, contract, train, and support thought leaders and faculty
• Steward speaker program content and peer-to-peer promotional assets
• Support congress strategy and execution, including product theaters, speaker engagement, promotional opportunities, and field support
• Measure and analyze program performance, thought leader feedback, customer engagement, speaker effectiveness, participation, and KPIs
• Lead materials through MAC review and manage agency/vendor workstreams, SOWs/POs, contracts, timelines, budgets, risk mitigation, and execution
• Monitor the AAV treatment landscape, customer feedback, competitors, scientific trends, and peer-to-peer best practices
• Use enterprise-approved AI tools to improve insight synthesis, content development, project management, and execution
• Identify test-and-learn opportunities for thought leader engagement, speaker programs, congress impact, and customer education

Senior Marketing Manager, Peer-to-Peer

Compliance

• Support regulatory submissions, site activation, and maintenance for awarded projects
• Plan, initiate, and track documents required for regulatory submissions
• Collect, review, and provide country, site, and ethics committee requirements
• Support end-to-end site start-up from site identification through site activation and maintenance
• Serve as the primary point of contact for sites and country-level regulatory and site activation activities
• Customize country-specific patient information sheets, informed consent forms, labels, and local regulatory documents
• Review and advise on country timelines
• Communicate submission status and action plans to the Regulatory Affairs Manager and project team
• Collect, receive, and perform initial reviews of study-specific site regulatory and essential documents
• Track regulatory documents by site and country and follow up as needed
• Identify country/site risks and develop mitigation strategies
• Advise on country regulatory strategies
• Maintain communication with sites to ensure timely completion of start-up and maintenance activities
• Provide updates on changing regulatory requirements and support interpretation of new regulations
• Maintain the regulatory intelligence database for the assigned country
• Comply with SOPs, ICH GCP, and applicable regulations
• Perform local quality control of submission dossiers when required
• Act as a contact point for translation review of submission documents
• Perform other assigned duties

Specialist, Regulatory and Site Activation

• Provide medical oversight of clinical trials to ensure SOPs, client directives, good clinical practice, and regulatory requirements are followed
• Manage and oversee contracted services
• Attend and present at investigator and sponsor meetings
• Provide medical consultation to clients, investigators, project team members, and internal team members
• Support business development activities
• Provide medical review and analysis of clinical trial serious adverse events
• Ensure tasks delegated to medical monitors are properly executed
• Monitor adverse events, laboratory abnormalities, patient medical status, concomitant medications, and un-blinding requests
• Discuss medical concerns with principal investigators and clients and apply medical judgment to clinical situations
• Medically review adverse events of special interest, serious adverse events, and clinical outcome events
• Perform data review and validation, including coding listings and safety data, to identify potential safety concerns
• Provide therapeutic and protocol training
• Write or review CSRs, IND/NDA reports, ICSRs, signal detection reports, periodic reports, RMPs, REMS, and CTD modules
• Manage signal detection activities and scientifically review aggregate reports
• Contribute to label updates, dossier maintenance, and risk management activities
• Medically review adverse-event and serious-adverse-event data from solicited, spontaneous, and literature sources

Medical Director/Senior Medical Director – Endocrinology

• Provide medical leadership and strategic support
• Partner with clients and cross-functional teams to strengthen relationships and drive successful clinical development programs
• Provide oversight, mentorship, and guidance to team members
• Contribute to key initiatives across Global Clinical Operations
• Contribute to development of company policies involving medical, safety, and therapeutics
• Participate in company-wide process improvement activities
• Provide leadership to staff within the therapeutic area
• Lead initiatives involving physicians across the therapeutic area
• Contribute to the vision and strategic direction of the therapeutic area
• Develop training modules and materials and provide disease-state and protocol-specific training
• Participate in training to advance knowledge of drug development and Good Clinical Practice (GCP) guidelines
• Provide subject matter and drug development expertise to medical strategy and client program execution
• Develop, review, and revise protocols, case report forms, training materials, project-specific tools, analysis plan designs, clinical trial reports, and new drug applications
• Provide medical and scientific expertise to project teams
• Act as Medical Monitor/study support for early clinical trials and handle medical and safety monitoring on assigned projects
• Interact with interdepartmental teams and external consultants
• Participate in feasibility discussions for project proposals
• Participate in project risk assessment activities
• Assist with Data Safety Monitoring Board activities when needed
• Provide clinical and medical expertise to other Fortrea departments
• Contribute to scientific and strategic leadership of a therapeutic area
• Perform other assigned duties

Account Manager

• Develop and grow key customer accounts through effective virtual engagement
• Build relationships with GPs, Practice Nurses, Community Pharmacists, Smoking Cessation Advisors and Public Health stakeholders
• Deliver compliant product and disease-area education focused on tobacco dependency and smoking cessation
• Identify account opportunities and create tailored business plans to drive growth
• Gather market insights and share customer feedback with internal stakeholders
• Collaborate effectively with cross-functional teams to maximise account performance
• Support healthcare professionals and patients on their smoking cessation journey
• Represent a market-leading smoking cessation and nicotine replacement portfolio

Senior Associate Paralegal – Trademark

Senior Medical Director – MD

Virtual Access Specialist

Virtual Pharmaceutical Sales Specialist

Senior Project Manager – Neurosciences, Psychiatry or Rare Diseases Team

Principal Specialist, Site Contracts

Auditor, RDQA Clinical Quality Audit

Senior Director, Customer Success – Resins and Technologies

Utilization Management Nurse Consultant

Medical Scribe

Senior Marketing Manager, Peer-to-Peer

Specialist, Regulatory and Site Activation

Medical Director/Senior Medical Director – Endocrinology

Senior Medical Director – MD

Virtual Key Account Manager