Precision Medicine Group

Clinical Research

• Manage and operationally deliver clinical elements of trials, including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out
• Execute assigned trials successfully and ensure completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials in collaboration with functional team members
• Mentor and train team members
• Identify challenges to study timelines and deliverables and propose creative action plans to the team and sponsor
• Lead CRAs in site relationships and oversight of monitoring, regulatory, IP, site payment, and site correspondence activities
• Maintain focus on study priorities through cross-functional partnerships and communication to achieve client satisfaction

Clinical Trial Manager

• Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out
• Execute assigned trials successfully and ensure completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials in collaboration with cross-functional team members
• Mentor and train team members
• Identify challenges to study timelines and deliverables and develop creative action plans for the team and sponsor
• Lead CRAs in establishing site relationships and overseeing monitoring, regulatory, investigational product, site payment, and site correspondence activities
• Maintain team focus on study priorities through cross-functional partnerships and effective communication to achieve client satisfaction

• Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out
• Execute assigned trials successfully and ensure completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials in collaboration with functional team members
• Mentor and train team members
• Identify challenges to study timelines and deliverables and propose creative action plans to the team and sponsor
• Lead CRAs in establishing site relationships and overseeing monitoring, regulatory, investigational product, site payment, and site correspondence activities
• Maintain focus on study priorities through cross-functional partnerships and effective communication to achieve client satisfaction
• Serve as the central intelligence hub for managed studies and lead CRAs across multiple countries

• Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out
• Execute assigned trials successfully and ensure completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials in collaboration with functional team members
• Mentor and train team members
• Identify challenges to study timelines and deliverables and develop creative action plans for the team and sponsor
• Lead CRAs in establishing site relationships and overseeing monitoring, regulatory, IP, site payment, and site correspondence activities
• Maintain team focus on study priorities through cross-functional partnerships and effective communication to achieve client satisfaction
• Serve as the central intelligence hub for managed studies and oversee clinical aspects across multiple countries

• Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out
• Execute assigned trials successfully and ensure completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials
• Collaborate closely with cross-functional team members
• Mentor and train team members
• Identify challenges to study timelines and deliverables and provide creative action plans to the team and sponsor
• Lead CRAs in site relationships and oversight of monitoring, regulatory, IP, site payment, and site correspondence activities
• Maintain focus on study priorities through cross-functional partnerships and effective communication
• Serve as the central intelligence hub for managed studies and oversee clinical aspects across multiple countries

Medical writer

• Lead the development of high-quality, on-time clinical study documents
• Plan, write, edit, format, and perform QC review of clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with Precision MW Style Guide, Precision SOPs, ICH, FDA, GCP, and eCTD requirements
• Manage documents from template through final approved version in collaboration with sponsors, external vendors, and internal Precision project teams/departments
• Independently formulate key messages from clinical study data
• Author complex content using relevant knowledge, skills, and process understanding
• Communicate clearly and concisely with internal and client teams, in writing and verbally
• Contribute to developing and maintaining medical writing processes, SOPs, templates, and work instructions
• Perform literature-based research to support writing activities
• Perform other duties as assigned

Senior Medical Writer/Principal Medical Writer

• Lead the development of high-quality and on-time clinical study documents
• Plan, write, edit, format, and perform QC review of clinical documents, including clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines, and eCTD requirements
• Ensure smooth and effective document management from template through final approved version in collaboration with sponsors, external vendors, and internal Precision project teams/departments
• Independently formulate key messages from clinical study data
• Author complex content using knowledge, skills, and understanding of processes
• Communicate clearly and concisely in writing and verbally with internal and client teams
• Contribute to the development and maintenance of medical writing processes, SOPs, templates, and work instructions
• Perform literature-based research to support writing activities
• Perform other duties as assigned

Senior Medical Writer / Principal Medical Writer

• Lead the development of high-quality and on-time clinical study documents
• Plan, write, edit, format, and perform QC review of clinical documents, including clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with Precision MW Style Guide, Precision SOPs, ICH, FDA, GCP, and eCTD requirements
• Formulate key messages from clinical study data independently
• Author complex content using knowledge of relevant processes
• Communicate with internal and client teams
• Ensure effective document management from template through final approved version in collaboration with sponsors, external vendors, and internal Precision teams/departments
• Contribute to medical writing processes, SOPs, templates, and work instructions
• Perform literature-based research to support writing activities
• Perform other duties as assigned

• Lead the development of high-quality and on-time clinical study documents
• Plan, write, edit, format, and perform QC review of clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines (ICH, FDA, GCP), and eCTD requirements
• Manage documents from template to final approved version in collaboration with sponsors, external vendors, and internal Precision project teams/departments
• Independently formulate key messages from clinical study data
• Author complex content using knowledge, skills, and process understanding
• Communicate clearly and concisely with internal and client teams
• Contribute to developing and maintaining medical writing processes, SOPs, templates, and work instructions
• Perform literature-based research to support writing activities
• Perform other duties as assigned

• Lead development of high-quality, on-time clinical study documents
• Plan, write, edit, format, and perform QC review of clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines, and eCTD requirements
• Manage documents from template through final approved version in collaboration with sponsors, external vendors, and internal Precision project teams/departments
• Independently formulate key messages from clinical study data
• Author complex content using knowledge of relevant processes
• Communicate clearly and concisely with internal and client teams
• Contribute to development and maintenance of medical writing processes, SOPs, templates, and work instructions
• Perform literature-based research to support writing activities
• Perform other duties as assigned

• Lead the development of high-quality and on-time clinical study documents
• Plan, write, edit, format, and perform QC review of clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with the Precision MW Style Guide, Precision SOPs, applicable regulatory guidelines (ICH, FDA, GCP), and eCTD requirements
• Manage documents from template through final approved version in collaboration with sponsors, external vendors, and internal Precision project teams/departments
• Independently formulate key messages from clinical study data
• Author complex content using knowledge, skills, and understanding of processes
• Communicate clearly and concisely with internal and client teams
• Contribute to medical writing processes, SOPs, templates, and work instructions
• Perform literature-based research to support writing activities
• Perform other duties as assigned

• Manage all aspects of the clinical trial data management process from study start-up through post-database lock for assigned projects
• Serve as primary Data Management contact and Lead Data Manager for assigned clinical projects/programs
• Oversee project data entry, including guidelines, training, quality, and resourcing
• Assess and manage timelines, deadlines, and resource needs
• Develop CRF specifications and coordinate stakeholder review and feedback
• Conduct database build UAT and maintain controlled database-build documentation
• Oversee clinical database quality and edit-check specifications
• Create, revise, version, and maintain data-management documentation and Trial Master File completeness
• Train clinical research personnel and data-management project team members
• Review and query clinical trial data according to the Data Management Plan
• Perform line-listing data review and patient/study-level status and metric reporting
• Perform medical coding and coordinate SAE/AE reconciliation
• Liaise with third-party data and EDC vendors regarding timelines and data deliverables
• Assist with SAS programming and quality control of SAS programs
• Identify and troubleshoot operational problems using metrics, audit reports, and stakeholder input
• Review and provide feedback on protocols, Statistical Analysis Plans, and Clinical Study Reports as required
• Participate in developing and maintaining SOPs and process documentation
• Participate in strategy meetings, bid-defense preparation, capability presentations, and client-engagement meetings
• Review RFPs, proposals, and project estimates
• Provide leadership for cross-functional and organization-wide initiatives
• Communicate with sponsors, vendors, and project teams regarding data and database issues
• Present software demonstrations, trainings, and project meetings
• Perform other duties as assigned; occasional travel may be required

Senior Clinical Data Manager

Account Executive

• Support client services efforts by connecting agency activities to clients
• Implement projects that promote and support the success and profitability of client deliverables
• Drive daily tasks by communicating with internal service delivery personnel and leading client communications
• Manage workflows for assigned accounts and ensure jobs are completed accurately and on time
• Develop and maintain account status reports and project timelines
• Contribute to project briefs and update clients and teams on schedules and next steps
• Own meeting decks and associated technology
• Review materials for accuracy and completion before client delivery, presentation, or final production
• Submit direct cost estimate requests and obtain client approvals
• Maintain organized project files
• Serve as a day-to-day client liaison and run status calls and meetings
• Foster client relationships and balance agency and client needs
• Assist with agency fee estimates, budgets, approvals, hour allocation, expenditure records, billing information, budget trackers, and billing forecasts
• Help move work through the agency to meet profitability goals and identify bottlenecks
• Develop product category, competitor, and key data-set knowledge
• Understand client objectives, target audiences, milestones, competitive landscape, clinical background, and performance metrics
• Identify opportunities to grow client business and billings
• Communicate the agency’s strategic and tactical point of view to clients

Account Executive, Pharmaceutical Advertising

• Acts as the business lead for the agency team and is responsible for all facets of assigned client business
• Carries out the client’s vision and advocates for agency solutions by aligning resources
• Leads cross-functional teams to deliver quality work and client satisfaction across multiple accounts
• Drives organic growth and growth of account team members
• Directs account teams to oversee tactics
• Provides guidance on high-profile and/or new strategy/deliverables
• Develops relationships with director-level and senior-level client partners and core brand teams
• Identifies client opportunities and issues early
• Manages forecasting, monthly and annual revenue recognition, pricing, revisions, and financial implications
• Reports changes to the financial picture and escalates revenue or forecasting upsides/downsides
• Develops product, category, competition, and client-market knowledge
• Provides strategic insights to internal and external teams
• Expands agency opportunities across client departments and divisions
• Participates in business development and networking initiatives
• Mentors junior staff and account teams
• Maintains relationships with senior-level industry executives
• Works cross-departmentally to manage issues and daily operations
• Represents the agency’s point of view at the highest levels of the client organization
• Provides leadership in challenging circumstances and supports business growth and issue mitigation

VP, Group Account Director

• Support and help manage strategic client accounts in partnership with Strategic Account Managers and/or Strategic Account Directors
• Contribute to strategic planning and develop annual strategic, tactical, brand, and project-level plans
• Manage day-to-day client communications and translate client vision into actionable plans and high-quality deliverables
• Oversee project execution and help ensure work is delivered on time, on budget, and aligned with client goals
• Support account financial management, including scoping, budgeting, forecasting, and monitoring team efficiency
• Identify opportunities to enhance client success, account growth, client advocacy, and new business
• Serve as day-to-day client contact on assigned accounts
• Coordinate internal teams on strategy, timelines, and client expectations
• Review deliverables for accuracy and readiness before client delivery
• Participate in and occasionally lead client meetings, status calls, planning calls, and calls with healthcare professionals
• Stay current on industry trends, scientific developments, regulations, and competitive landscapes
• Prepare client plans, respond to ad hoc requests, finalize materials, prepare content, and support live client or healthcare professional meetings, including travel when needed

Clinical Trial Manager

Clinical Trial Manager

Clinical Trial Manager

Clinical Trial Manager

Clinical Trial Manager

Senior Medical Writer/Principal Medical Writer

Senior Medical Writer / Principal Medical Writer

Senior Medical Writer/Principal Medical Writer

Senior Medical Writer / Principal Medical Writer

Senior Medical Writer / Principal Medical Writer

Senior Medical Writer/Principal Medical Writer

Senior Clinical Data Manager

Account Executive, Pharmaceutical Advertising

VP, Group Account Director

Strategic Account Associate, Medical Communications