Precision Medicine Group

Content Writer

• Use data, SME insights, and generative AI tools to produce high‑quality drafts for B2B content including blogs, ads, landing pages, emails, video scripts, social posts, and press releases.
• Build and refine prompts, content templates, and repeatable workflows optimized for AQ’s brand language and message consistency.
• Rapidly iterate and explore creative variations to support campaign experimentation, A/B testing, and channel‑specific optimization.
• Support website content updates, product positioning, editorial calendar planning, and event and conference content.
• Edit, refine, and elevate content generated by AI tools and internal SMEs, ensuring clarity, accuracy, and alignment with AQ’s brand standards.
• Ensure all content meets Precision AQ’s brand voice, terminology standards, tone, and narrative expectations.
• Translate complex healthcare, commercial/market access, and scientific subject matter into clear, compelling, and credible content.
• Partner closely with design to ensure visual and verbal alignment across campaigns and assets.
• Maintain a content quality bar, ensuring accuracy, brand language, grammar, and consistency.
• Collaborate with Marketing Operations to understand content performance data and apply insights to improve future content.
• Operate effectively in a fast‑moving environment with evolving inputs and priorities, maintaining clarity and momentum even when direction evolves or details are ambiguous.

Senior Content Writer – B2B Marketing

Graphics Designer

• The Senior Graphic Designer (SGD) is responsible for developing high quality, strategically grounded visual communications for pharmaceutical and healthcare clients.
• Designing and producing high quality print, digital, and PowerPoint materials in support of Market Access initiatives (e.g., payer marketing, value tools, launch materials, unbranded/above brand campaigns)
• Translating complex scientific, economic, and access narratives into clear, engaging visual storytelling
• Ensuring accuracy, consistency, and brand alignment across all deliverables
• Applying knowledge of Market Access and Managed Markets audiences to creative decision making
• Participating in concept development and iterative refinement based on strategic objectives and stakeholder feedback
• Proactively proposing new approaches, layouts, or visual systems to enhance clarity and impact
• Partnering closely with Account, Medical, Strategy, and Project Management teams to deliver on time and on brief
• Incorporating medical/legal/regulatory feedback accurately and efficiently
• Managing multiple projects simultaneously with minimal supervision
• Taking ownership of assigned workstreams from concept through production.

Senior Graphic Designer

Frontend Engineer

• Develop custom Drupal modules and themes
• Configure and maintain Drupal CMS features and content structures
• Translate business requirements and creative designs into functional Drupal solutions
• Implement third-party integrations (APIs, marketing tools, CRM systems, etc.)
• Maintain and update legacy Drupal codebases
• Participate in architecture discussions and technical planning
• Perform code reviews and contribute to best practice standards
• Support deployment processes and troubleshoot production issues
• Optimize Drupal performance and caching configurations
• Code, test, and support database-driven web applications
• Provide technical assistance to creative and UX teams as needed
• Assist in producing accurate tasks and project estimates
• Recommend solutions based on best practices and independent judgment
• Stay current on Drupal core updates, contributed modules, and security releases
• Contribute to documentation and internal knowledge sharing

Web Developer

CRC 23,692,400 - CRC 35,538,600 per year

Manager

• Perform allocation and assignment of global resources in complex staffing scenarios for multiple departments
• Work with stakeholders and senior leadership to understand complex resource requirements
• Identify strategies to meet current and future needs
• Proactively identifies capacity constraints and hiring needs for department leaders
• Negotiates and resolves staffing conflicts in collaboration with stakeholders
• Partners with department leadership on implementing process improvements and initiatives
• Prepare metrics and summary reports on resourcing activities as necessary
• Escalate sensitive or high-risk staffing situations to Resource Management leadership and Executive Team as necessary
• Mentors others when required
• Supports leadership with strategy
• Other duties as assigned

Senior Resource Manager

Financial Planning and Analysis

• Support the project teams in all financial areas associated with running a clinical trial.
• Assist in the preparation of the monthly invoicing worksheet which is the source document for client invoicing and source of revenue recognition
• Perform variance analysis comparing forecasted revenue to actual revenue to identify gaps, changes in scope, etc.
• Review work orders and change order budgets in comparison with actual activities to help identify out of scope activities
• Perform monthly Earned Value Analyses (EVA’s) in conjunction with the Project Directors/Project Managers. Participate in the monthly project review meetings on an as needed basis
• Provide support to the Executive Director of Operational Finance in the preparation of contract documents (statements of work and change orders)
• Work with Company Accountant to provide support to the financial reporting and general ledger functions. Work with Company Accountant to provide support to ensure an accurate and timely monthly, quarterly and year-end close
• Work with Company Accountant to ensure the timely reporting of all monthly financial information. Collaborate with others in Finance to support overall department goals and objectives
• Responds to inquiries from the CFO and Executive Director of Operational Finance regarding financial results, special reporting requests and ad hoc analyses relating to projects
• Assist in development and implementation of new procedures and features to enhance the workflow and internal controls

Senior Financial Analyst

Director

• Provide specific healthcare expertise and relevant experience for strategy and execution of client projects
• Represent the Access Experience Team to clients and lead payer strategy work to identify and meet clients’ business needs
• Support cross-functional matrix teams in support of internal and external client deliverables
• Provide segment strategy input for prelaunch and existing brand, biosimilar, or loss of exclusivity business planning
• Assist new business development through research, proposal development, and presentation
• Contribute by providing industry specific expertise to related projects
• Support and present education and training of either customer or internal personnel as required
• Conduct interviews with advisors to understand current market dynamics and prepare summaries for client projects
• Assist in preparation and execution of client workshops and competitive simulations. Role-play as payer or other healthcare stakeholder during exercise to enhance client understanding of market challenges.
• Review evolving market trends in drug coverage landscape and provide actionable insights to Precision Payer and Account team leads.
• Prioritize deliverables across multiple clients and assist team in meeting tight deadlines.
• Represent Precision at industry meetings and gather insights relevant to clients.
• Assist account team in budget planning with client(s) and providing recommendations on services/projects to meet client needs.
• Create or curate internal and external training materials related to managed market core subject matter or current events
• Other duties as assigned
• Travel up to 50%

Senior Director, Access Experience

Account Executive

• Understand the business challenges your client is facing and what strategic questions they are or should be asking
• Help clients define and achieve their business goals
• Prepare annual strategic/tactical plans for each client and individual campaign/project plans as needed throughout the year
• Manage and strengthen client relationships
• Propose, sell to clients, and oversee ideas and projects that are tied to clients’ objectives
• Continuously offer unsolicited ideas to increase the effectiveness of clients’ brand and company activities
• Initiate and oversee Precision AQ activities on behalf of and in support of clients
• Manage day-to-day client-Precision AQ communication on strategy (ideas, recommendations, approaches to consider) and planning
• Closely manage clients’ budget and team efficiency to maximize return for clients and Precision AQ
• Work with the internal team to exceed clients’ expectations
• Mentor, train, and coach team members to facilitate growth and development
• Stay abreast of developments (eg, science, competitors, regulations) in clients’ industries.

Strategic Account Associate – Medical Communications

Compliance

• Lead and maintain GCP quality assurance programs to ensure compliance with FDA, EMA, and ICH regulatory requirements.
• Provide ICH/GCP compliance guidance throughout the clinical development life cycle.
• Plan, oversee, and conduct GCP audits including but not limited to qualification and re-qualification of vendors, internal process, site, TMF and other document audits.
• Manage Quality and Compliance functional activities, including implementation and management of the QMS, inclusive of SOPs, Training and CAPAs.
• Work closely with the Quality and Compliance staff and Operational Functions to provide strategic compliance advice and guidance.
• Initiate the process of follow-up when suspicion of suspected scientific misconduct/serious non-compliance.
• Review clinical and nonclinical documentation to ensure regulatory compliance, data integrity, and adherence to GCP standards.
• Oversee quality events, deviations, and CAPA processes related to GCP activities.
• Lead and support global health authority inspections.
• Provide GCP guidance and training to cross-functional teams to promote a culture of quality and regulatory compliance.
• Lead and develop Clinical QA staff while supporting continuous improvement of GCP and quality systems.
• Supervisory responsibility of Quality & Compliance employees (where applicable).

Senior Director, Quality & Compliance

Project Manager

• Works cross functionally to develop partnership strategies for clinical trials and programs and works closely with our project teams to provide oversight, strategic expertise in the planning, coordination, and delivery of all activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.
• Direct, manage and ensure collaboration within a team Project Directors and Project Managers in the planning, execution and governance of projects/portfolios on a global platform.
• Provide leadership and oversight on all clinical programs and in some unique cases, manage activities.
• Interact with study sponsors as primary point of escalation beyond project management.
• Optimize the profitability of the Project Management organization to meet or exceed budget targets.
• Assess and manage resource allocations to ensure that established cost, time, and quality goals are met.
• Select, train, develop and manage the performance of talent in project leadership positions (Project Directors and Project Managers).
• Provide technical support and guidance (including scope definition, risk identification, escalation and mitigation, resource planning, goals and deliverables) to assigned project managers.
• Identify and escalate impacts to project scope, resources, schedule or budget through standard methods.
• Ensure project leadership personnel work to the highest quality standards and maintain compliance with established SOPs, working guidelines, project plans and all regulatory requirements.
• Participate with Business Development in opportunity development, proposals and budgeting, bid defense preparation and attendance.
• Understand and manage project/program inter-dependencies to achieve program milestones/deliverables.
• Conduct evaluations and implement required changes for all projects (including mid-project recovery of at risk projects, re-scoping, postponement, or cancellation).
• Measure and report KPIs and lead continuous improvement.
• Recognize, exemplify and adhere to Precision’s values that center on our commitment to quality, our people, clients and performance.
• Manage workload of supervised staff with continued assessment and adjustment as needed.
• Provide on-going feedback, development and coaching of Project Directors and Project Managers including annual performance reviews.

Director, Project Management – Oncology

Research Analyst

• The CRA II provides overall support to study sites and clinical project teams engaged in clinical research studies.
• Oversees all aspects of study site management to ensure patient safety is protected.
• Provides guidance at the site and project level towards audit readiness standards.
• Updates, tracks and maintains study specific trial management tools/systems, and status reports.
• Independently conducts all forms of site visits, including pre-study/qualification, initiation, routine monitoring, and close-out visits.
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents.
• Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management.

Clinical Research Associate II

• Works cross functionally to develop partnership strategies for clinical trials and programs
• Works closely with our project teams to provide oversight, strategic expertise in the planning, coordination, and delivery of all activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.
• Direct, manage and ensure collaboration within a team Project Directors and Project Managers in the planning, execution and governance of projects/portfolios on a global platform
• Provide leadership and oversight on all clinical programs and in some unique cases, manage activities
• Interact with study sponsors as primary point of escalation beyond project management
• Optimize the profitability of the Project Management organization to meet or exceed budget targets
• Assess and manage resource allocations to ensure that established cost, time, and quality goals are met
• Select, train, develop and manage the performance of talent in project leadership positions (Project Directors and Project Managers)
• Provide technical support and guidance (including scope definition, risk identification, escalation and mitigation, resource planning, goals and deliverables) to assigned project managers
• Identify and escalate impacts to project scope, resources, schedule or budget through standard methods
• Ensure project leadership personnel work to the highest quality standards and maintain compliance with established SOPs, working guidelines, project plans and all regulatory requirements
• Participate with Business Development in opportunity development, proposals and budgeting, bid defense preparation and attendance
• Understand and manage project/program inter-dependencies to achieve program milestones/deliverables
• Conduct evaluations and implement required changes for all projects (including mid-project recovery of at risk projects, re-scoping, postponement, or cancellation)
• Measure and report KPIs and lead continuous improvement
• Recognize, exemplify and adhere to Precision’s values that center on our commitment to quality, our people, clients and performance
• Manage workload of supervised staff with continued assessment and adjustment as needed
• Provide on-going feedback, development and coaching of Project Directors and Project Managers including annual performance reviews

Director, Project Management – Autoimmune

• Serve as primary point-of-contact and primary escalation point to the client
• Coordinate and oversees all functional services including external vendors to the established timeline and budget
• Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate. Independently drive the CO to completion and execution with support as needed.
• Maintain integrated collaboration with clinical operations in the delivery and participates in clinical activities as appropriate. For projects of very limited scope (i.e. number of sites), Sr. PM may assume all clinical activities
• Manage the financial health of assigned studies, including oversight of the project profitability, billable project hours, and compliance with on time, accurate billing and forecasting to support business objectives.
• Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality
• Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings.
• Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation
• Establish tracking metrics to monitor trial and team progress towards project goals
• Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise
• Leads both internal and client meetings and set expectations for the project team
• Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues
• Ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients including Bid Defenses with proficiency
• Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project
• Support business development and marketing activities as appropriate, including travel to Bid Defense meetings as required
• Perform other duties as assigned by management
• Remain compliant with organizational training, time-reporting and any other administrative duties as required
• Provides on-going feedback, for functional team members including annual performance reviews

Senior Project Manager – Autoimmune

Business Development Rep

• Design and implement relationship development and future sales planning within strategic accounts
• Identify leads, qualify targeted oncology and rare disease Sponsors
• Strategically coordinate members of the Executive Team across PMG to leverage their expertise
• Represent the company at trade shows and client-sponsored events
• Work closely with Corporate Marketing to implement a Marketing program
• Develop and maintain relationships with partner organizations
• Update Salesforce for metric driven reporting
• Provide regular feedback to the Executive Team on pricing, competitiveness, and market conditions

Business Development Director

Medical writer

• Under direct supervision, develop high quality, medically accurate content in print or digital format for a wide range of medical communication resources
• Deliver requested projects per established timelines
• Conduct literature reviews and develop annotations to support promotional claims in a variety of promotional medical education and marketing resources
• Ensure professional, proactive, and collaborative communication with internal and external stakeholders
• Ensure a constant high quality of work in line with science, good publication practice, and company rules and policies
• Work closely with account teams to refine content in keeping with strategic imperatives
• Communicate medical content with internal team and pharmaceutical clients, as necessary
• Attend medical, legal, regulatory review meetings, as necessary
• Participate in all internal team meetings, including project kick-off meetings, weekly status meetings, client meetings, and internal brainstorm/review meetings
• Contribute ideas for tactical planning within assigned accounts
• Promote and adhere to Precision Value and Health’s workplace values known as PRECISION Principles (Client Service, Purpose, Accountability, Mutual Respect and Collaboration)

Medical Writer, Patient Support

• Monitor and own the progress of clinical studies at investigative sites
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
• Coordinate all necessary activities required to set up and monitor a study