Jobs at Precision Medicine Group

Lead on-site laboratory operations across Bioanalysis, Flow Cytometry and Companion Diagnostics. Ensure regulatory-compliant assay development (FDA/IVDR, CLIA, CLSI, ISO), manage lab heads, drive operational excellence, budget and KPI reporting, client communication, QA/regulatory interactions, and mentor technical staff.

Process and triage ICSRs for clinical and post-marketing programs, enter data into Argus, code events/medications, draft narratives, reconcile safety data, generate expedited reports, maintain regulatory compliance and TMF documentation, and support audits and project meetings.

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The Proposals and Budgeting Systems Manager will support financial tool development and maintenance, assist departments, manage budgeting algorithms, and ensure effective operational tools and training.

Perform and troubleshoot molecular biology assays (DNA/RNA extraction, qPCR, NGS) under CLIA/GLP/GCP standards. Maintain reagents, instruments, QC, documentation and SOPs; train staff and support assay development, validation, and cross-functional process improvements. Flexible shift work required.

The Senior Feasibility Associate conducts global feasibility analyses, supports clinical trials, and manages feasibility projects involving site selection and client interaction.

Lead client account activities for pharmaceutical payer marketing programs. Manage project scope, timelines, budgets, and cross-functional teams; liaise with clients daily; coordinate pitches, MLR review, content planning, and financial/forecast reporting to ensure successful, compliant deliverables and identify growth opportunities within accounts.

Supports clinical study sites and project teams across LATAM by maintaining essential study documentation, tracking activities in CTMS/EDC/TMF, liaising with sites, assisting with site selection and regulatory submissions, and supporting monitoring and logistics tasks while ensuring compliance with ICH-GCP and sponsor SOPs.

Lead and grow market access consulting services for life sciences clients, drive business development and revenue, manage client engagements, and develop consulting staff. Provide strategic direction across payer, provider, and patient access solutions, support hiring and culture, and collaborate cross-functionally to expand services.

Manage and negotiate clinical study budgets and a variety of clinical research agreements (NDAs, CTAs, amendments). Coordinate contract execution, maintain contract files/databases, update study teams, resolve contractual issues, and improve contracting processes while working with global clinical operations.

Lead and execute GCP process audits, vendor and site assessments, and TMF audits. Support QA systems (SOPs, training, CAPA), host sponsor audits and inspections, participate in computer systems validation, manage quality issues and CAPAs, and provide QA consultation to project teams ensuring compliance with GCP/ICH, FDA, and company procedures.

Lead and execute GCP process audits, support QA systems (SOPs, CAPA, training), host sponsor/client audits and inspections, conduct vendor/site/TMF/internal audits, support CSV and change control, provide QA consultation, manage quality issues and CAPAs, and monitor compliance with GCP/ICH/FDA and company procedures.

Lead and perform GCP process, site, vendor, TMF, and internal audits; support QMS (SOPs, training, CAPA); host sponsor audits and inspections; advise project teams, manage quality issues, participate in CSV and systems change control, and maintain QA metrics and documentation.

Lead and perform GCP process, vendor, site, TMF and internal quality audits; support QMS (SOPs, training, CAPA), host sponsor audits and inspections, assist CSV and change control, provide QA consultation to project teams, monitor quality metrics, and manage corrective actions to ensure regulatory compliance.

Lead and execute GCP process audits and assessments across clinical studies, vendors, and internal quality systems. Support QMS activities (SOPs, CAPA, training), host sponsor/client audits and regulatory inspections, participate in computer system validation, provide QA consultation to project teams, maintain quality trackers/metrics, and identify compliance risks and improvements.

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.

Serve as the primary IT–business liaison, owning executive relationships, technology strategy, vendor management, and prioritization of IT/AI initiatives. Drive modernization, cost/benefit analyses, budgeting, continuous improvement, and successful deployment of technology solutions across business units.

Assist with study startup documents, coordinate with teams, document customer requirements, and ensure compliance with standards. Develop project specifications and support internal relationships.