Precision Medicine Group

20 open remote positions

Precision Medicine Group is a healthcare consulting and services firm specializing in pharmaceutical cost and coverage solutions. They foster a collaborative culture focused on client delivery and innovation, with a team of consultants and analysts supporting top healthcare leaders.

Salary Distribution 8 of 20 jobs

Benefits Overview 8 of 20 jobs

Health Insurance (8) Life Insurance (8) Parental Leave (8) Retirement Savings (8) PTO (6) Disability Benefits (4) Disability (2) Disability Insurance (2) Bonus (1) Paid Time Off (1)

Open Positions

  • Support project teams in translating patient engagement strategies into practical, study-level plans and deliverables.
  • Assist in development or coordination of patient engagement materials aligned with literacy and diversity guidelines.
  • Coordinate with vendors and internal teams to ensure positive patient experience and inclusive representation.

  • Provide operational leadership and oversight for assigned FSP projects, managing regional trials or supporting complex global trials.
  • Serve as the primary operational point of contact for clients, coordinating cross-functional activities and monitoring project risks, resource constraints, and quality trends.
  • Contribute to financial oversight, meeting facilitation, and team onboarding, training, and mentoring.

$162,000–$243,000/yr

  • Identify and develop new business opportunities for biospecimen products and services, with a focus on biofluids, tissues, and specialty lab services.
  • Build and maintain relationships with key clients, retain existing accounts, and explore cross-selling within the Precision Translational Sciences portfolio.
  • Attend conferences, manage leads via CRM, and collaborate with internal teams to close new business and expand existing relationships.

  • Lead development of high-quality clinical study documents including protocols, IBs, ICF, DSURs, CSRs, and patient narratives.
  • Ensure smooth document management from template to final approval in collaboration with sponsors and internal teams.
  • Independently formulate key messages from clinical data and author complex content with impeccable attention to detail.

$68,700–$103,100/yr

  • Review, draft, negotiate, and track legal agreements including clinical trial agreements (CTA), confidentiality disclosure agreements (CDA), and site budgets.
  • Lead interactions with internal study teams, sites, and sponsors across North America and Europe to resolve contractual issues and ensure alignment with timelines.
  • Maintain contract files and databases, coordinate execution, and update stakeholders on negotiation status.

$147,300–$220,900/yr

  • Serve as primary point-of-contact and escalation point for clients, coordinating all functional services and external vendors.
  • Manage study budgets, project profitability, and billing compliance to ensure financial health and alignment with scope.
  • Develop robust project plans, track metrics, and prepare status updates for clients and senior management.

$75,600–$113,400/yr

  • Develop safety management plans and oversee serious adverse event case management from intake to regulatory reporting.
  • Perform intake, triage, data entry, medical coding, and narrative composition for individual case safety reports.
  • Provide safety training, review standard operating procedures, and assist clients with safety-related reviews.

  • Lead the development and optimization of clinical data systems, driving data standardization and building scalable validation frameworks.
  • Architect high-performance databases and ETL pipelines, integrating data from diverse clinical systems across global trials.
  • Serve as a strategic liaison between Biostatistics, Clinical Operations, and Regulatory Affairs to translate clinical requirements into technical solutions.

  • Act as primary clinical point of contact with clients and lead planning, execution, and oversight of clinical studies across Latin America.
  • Develop country-level recruitment strategies, guide monitoring and quality strategies, and mentor CRAs and partners.
  • Collaborate with project managers on budgets, vendor management, and ensure compliance with ICH-GCP and regulatory requirements.