Precision For Medicine

Business Development Rep

• Design and implement relationship development and future sales planning within strategic accounts, supporting program development and repeat business from biotech and pharmaceutical companies
• Identify leads and qualify targeted oncology and rare disease sponsors
• Conduct introductory and follow-up meetings with prospective clients and Regional Vice Presidents of Business Development
• Secure RFPs and collaborate with Business Operations, Proposal Team, and other staff to create proposals for new business
• Coordinate Executive Team members across PMG to leverage expertise and bring in new business
• Find innovative ways to work across business units to sell PMG services
• Represent the company at trade shows and client-sponsored events
• Collaborate with Corporate Marketing and Executive Team members to design and implement marketing programs supporting sales
• Develop and maintain relationships with partner organizations, including data management companies, other CROs, and related organizations
• Update Salesforce or other metrics-tracking software to provide metric-driven reporting for company leadership
• Provide regular feedback to the Executive Team on company positioning, pricing, competitiveness, and market conditions
• Maintain close contact with key sponsor personnel to ensure client expectations are met or exceeded
• Serve as the main point of contact for external clients and potential partners
• Assist in program development for strategic alliances

Director, Business Development

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 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 or 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 of 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 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 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 offer 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 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 study timeline and deliverable challenges and offer 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 communication to achieve client satisfaction

• Manage and operationally deliver clinical elements of 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 provide creative action plans to the team and sponsor
• Lead CRAs in establishing site relationships and overseeing monitoring, regulatory, IP, site payment, and site correspondence activities
• Maintain focus on study priorities through cross-functional partnerships and communication to achieve client satisfaction

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 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

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 study protocols, IBs, ICF templates, DSURs, CSRs, and CSR patient narratives
• Develop documents in compliance with the Precision MW Style Guide, Precision SOPs, 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
• Formulate key messages from clinical study data independently
• 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

Senior Medical Writer – Principal Medical Writer

• 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, ICH, FDA, GCP, and eCTD requirements
• Manage documents from template through final approved version in collaboration with sponsors, external vendors, and internal Precision 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 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 development of high-quality, 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
• 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 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, 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 process understanding
• 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

• 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 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 process understanding
• Communicate clearly and concisely in writing and verbally 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

Senior Medical Writer, Principal Medical Writer

• Manage all aspects of the clinical trial data management process from study startup through post-database lock for assigned projects
• Follow SOPs/WIs, regulatory directives, study-specific plans, and guidelines
• Serve as primary Data Management contact or Lead DM 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 when required
• Conduct database build UAT and maintain controlled database documentation
• Oversee clinical database quality and edit-check specifications
• Create, revise, version, and maintain data management documentation and Trial Master File documentation
• 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 external data and EDC vendors regarding timelines and data-related deliverables
• Assist with SAS programming and quality control of SAS programs when needed
• Identify and troubleshoot operational problems using metrics, audit reports, and stakeholder input
• Review and provide feedback on protocols, SAPs, and CSRs when required
• Participate in SOP and process documentation development and maintenance
• Support strategy meetings, bid defenses, capability presentations, client engagement meetings, RFP reviews, proposals, and project estimates
• Provide leadership for cross-functional and organization-wide initiatives
• Communicate with sponsors, vendors, and project teams regarding project issues
• Present software demonstrations, trainings, and project meetings
• Perform other assigned duties

Senior Clinical Data Manager

Accounting Manager

• Oversee month-end close processes, inventory accounting, revenue recognition, and financial reporting
• Review journal entries and prepare complex general ledger entries as required
• Review accounts payable spend and cash flow forecasts
• Review balance sheet account reconciliations across multiple business units and prepare complex reconciliations as needed
• Partner with FP&A on budgets, forecasts, and allocation methods
• Train and mentor staff and ensure accounting process documentation is shared with the business
• Identify process improvement opportunities and integrate new business acquisitions
• Monitor emerging US GAAP standards and assist with data gathering and implementation
• Review financial results for efficiencies and establish internal controls to minimize payment errors, duplicate payments, and fraud
• Review customer contracts for consistent revenue recognition under US GAAP (ASC 606)
• Prepare and review audit support, accounting memos, audit schedules, and PBC requests; support statutory audits and follow up on audit issues
• Assist with strategic initiatives including system implementations, integrations, and acquisitions
• Perform other duties assigned by the line manager

Manager

• Develop client-focused budgets and proposals for Phase I–IV clinical trials
• Map simple bid grids with manager support
• Collaborate with global operational review teams on budgets and proposals responding to client RFPs
• Prepare budgets, proposal text, and re-bids for global opportunities
• Coordinate the full RFP preparation process and ensure accurate, timely deliverables
• Review client RFP documents and identify service requirements and assumptions
• Coordinate and lead RFP development meetings with sales, operational review, and finance teams
• Develop project budgets using costing tool templates and Excel-based formulas
• Prepare proposal text using departmental templates and reflect client needs and strategic assumptions
• Coordinate with partners and third-party vendors during RFP development
• Perform quality control of budget and proposal text edits
• Support work orders and RFIs
• Respond to client questions regarding budgets and operational strategy
• Participate in client meetings as needed
• Maintain departmental records and internal/intercompany reporting
• Participate in departmental initiatives and perform other duties as needed

Director, Business Development

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

Accounting Manager

Proposals Manager – Senior