Jobs at Precision Medicine Group

Supports payer marketing account teams for pharmaceutical and life sciences clients by coordinating projects, timelines, budgets, client communications, content planning, and medical-legal-regulatory reviews. The role manages project scope and roadblocks, prepares client reports and financial forecasts, and contributes to proposals and marketing communication programs. Candidates need a marketing, communications, or advertising degree plus at least one year of relevant agency experience or an internship.

Conduct secondary and primary research for pharmaceutical and biotech clients on pricing, reimbursement, market access, and value communication. Develop research materials, interview healthcare stakeholders, perform quantitative and qualitative analyses, and create client-ready presentations with actionable recommendations. Collaborate with senior consultants and global teams in a flexible consulting environment.

Lead statistical planning, analysis, and regulatory strategy for clinical development programs. Author and review protocols and statistical analysis plans, perform sample size and randomization work, support DMC reporting, mentor statisticians, and provide SME oversight for complex submissions (NDA/BLA/MAA) and advanced methodologies like Bayesian adaptive designs and survival analysis.

Provide statistical leadership across all clinical development phases: consult on study design and regulatory strategy, author and review protocols and complex statistical analysis plans, perform and review analyses, prepare submissions (NDA/BLA/MAA), serve as SME (e.g., Bayesian methods, survival analysis), support DMC reporting, mentor statisticians, and coordinate with sponsors and vendors.

Manage clinical trial safety activities, including safety management plans, serious adverse event and SUSAR case processing, medical coding, expectedness assessments, narratives, regulatory reporting, quality control, safety database setup, reporting plans, training, and oversight. Collaborate with sponsors, vendors, clients, study sites, and internal teams while ensuring compliance with FDA, ICH, and global safety regulations.

Manages financial oversight for a client portfolio, including project accounting, forecasting, budgeting, revenue recognition, invoicing, accruals, reconciliations, audits, and monthly reporting. The role supervises client finance staff, reviews contracts and project financials, supports GAAP and ASC 606 compliance, coordinates with FP&A and legal teams, manages intercompany transactions and subcontractor costs, and leads process improvements and staff development.

The Feasibility Manager conducts evidence-based assessments for clinical trials, analyzing protocols, recruitment history, epidemiology, site capabilities, patient pools, and operational risks. They translate findings into country, site, enrollment, and recruitment recommendations; present analyses to clients and internal stakeholders; coordinate site and investigator outreach; support bid defenses; and improve feasibility methods, tools, data sources, and best practices. The role requires cross-functional collaboration across clinical operations, medical, business development, and external partners.

Leads clinical trial feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements. Reviews protocols and operational plans; analyzes recruitment history, epidemiology, treatment landscapes, countries, sites, and patient pools; and develops evidence-based recommendations. Presents findings to clients and internal stakeholders, coordinates site and investigator outreach, collaborates cross-functionally, and contributes to feasibility methods, tools, data sources, and team development.

Lead and support clinical trial feasibility assessments across global studies. Review protocols, analyze recruitment, epidemiology, site, country, patient-pool, and operational data, and translate findings into evidence-based recommendations. Present analyses to internal stakeholders and clients, coordinate site and investigator outreach, support bid defenses, and improve feasibility methods, tools, data sources, and best practices. Collaborate across Business Development, Clinical Operations, Medical, investigators, consultants, and data partners.

Leads clinical trial feasibility assessments by reviewing protocols, analyzing recruitment, epidemiology, site, country, and patient-pool data, and developing operational recommendations. Presents findings to clients and internal stakeholders, coordinates site and investigator outreach, supports bid defenses, and improves feasibility methods, tools, and best practices. Collaborates across clinical operations, medical, business development, consultants, investigators, and data partners on global studies.

Leads clinical-trial feasibility assessments by reviewing protocols, analyzing recruitment, epidemiology, site, country, patient-pool, and competitive data, and translating evidence into operational recommendations. Presents findings to clients and internal stakeholders, coordinates site and investigator outreach, manages deliverables, identifies feasibility risks, and contributes to methods, tools, best practices, and team development across global clinical programs.

Lead and support clinical trial feasibility assessments by reviewing protocols, analyzing recruitment, epidemiology, site, country, and patient-pool data, and developing evidence-based recommendations. Present findings to internal stakeholders and clients, coordinate site and investigator outreach, contribute to bid-defense discussions, and improve feasibility methods, tools, data sources, and best practices across global clinical development programs.

Lead and support clinical-trial feasibility assessments across global studies. Review protocols, analyze recruitment, epidemiology, site, country, and patient-pool data, and translate findings into evidence-based recommendations. Present analyses to internal teams and clients, coordinate site and investigator outreach, support bid defenses, identify feasibility risks, and improve methods, tools, data sources, and best practices. Collaborate across Business Development, Clinical Operations, Medical, consultants, investigators, and sites.

Supports financial management for a client portfolio, including project accounting, reconciliations, revenue recognition, forecasting, invoicing, accruals, intercompany transactions, month-end close, audits, and budgeting. The role reviews contracts, project costs, expenses, and financial trackers; coordinates with project managers and finance teams; mentors junior staff; and helps improve department policies and procedures.

Bridges clinical, business, innovation, and technology teams to improve processes and implement AI-enabled solutions. Gathers requirements, documents functional specifications, supports system configuration, integrations, releases, testing, UAT, training, and adoption. Develops AI agents, prompt libraries, SOPs, work instructions, and governance resources. Provides strategic system recommendations, supports audits and CAPA activities, and drives operational efficiency across clinical trial systems.

Produces recurring and ad hoc commercial operations reports, dashboards, and KPI analysis covering pipeline, forecasting, bookings, and performance. Maintains Salesforce data quality, analyzes pipeline health and forecasting trends, supports executive business reviews, and contributes to reporting automation, business intelligence, process improvement, and strategic commercial projects.

Lead and manage market access consulting projects: direct teams, run primary research with payers and clinicians, synthesize insights, develop pricing and access strategies, build client relationships, and contribute to practice development and training.

The Site Contracts Manager will review, draft, negotiate, and track various legal agreements in the clinical research context, ensuring compliance with policies and managing contractual issues.

The Senior Data Engineer will develop data ingestion, transformation, and enrichment pipelines, ensuring data quality and reliability. Responsibilities include creating Bronze and Silver data layers, using SQL and dbt for implementation, and collaborating with architects and stakeholders to align data solutions with enterprise standards.

The Site Contracts Manager drafts, negotiates, and tracks various legal agreements for clinical studies, ensuring alignment with timelines and company standards.