Clinical Research Project Manager

Mass General BrighamSomerville, MA
$63,253 - $102,596Hybrid

About The Position

We are seeking a Clinical Research Project Manager to help lead and coordinate industry-sponsored clinical research initiatives from startup through execution. In this role, you will serve as a key connection point among investigators, research teams, sponsors, and institutional stakeholders—helping studies move forward efficiently, thoughtfully, and in alignment with project goals. This is an opportunity for a highly organized, collaborative project manager to contribute to research growth, operational excellence, and meaningful stakeholder engagement. You will manage timelines, coordinate cross-functional work, support process improvements, and help ensure that research projects are delivered with clarity, accountability, and high-quality communication.

Requirements

  • Bachelor’s degree in a related field required.
  • 3–5 years of research-related experience required.
  • Strong organizational and communication skills.
  • Demonstrated analytical skills.
  • Effective problem-solving skills.
  • Strong computer skills.

Nice To Haves

  • Experience in lieu of a degree is not accepted.

Responsibilities

  • Plan, coordinate, and execute clinical research projects and initiatives that support industry-sponsored research, investigator engagement, and research growth.
  • Develop and manage project plans, timelines, milestones, deliverables, dependencies, and risk mitigation strategies to keep projects on track.
  • Bring together cross-functional teams, including investigators, research operations, data and analytics teams, sponsors, and institutional stakeholders.
  • Monitor project progress against goals, proactively identify barriers, escalate risks, and help implement solutions.
  • Serve as the central point of coordination for assigned projects, helping stakeholders stay aligned and accountable for deliverables.
  • Facilitate project meetings, working sessions, and governance discussions; document decisions, track action items, and ensure timely follow-through.
  • Create and maintain project documentation, status reports, dashboards, and leadership communications that support transparency and informed decision-making.
  • Collect, review, and support completion of regulatory and operational documentation required for study startup and implementation.
  • Contribute to improvement initiatives focused on research efficiency, stakeholder engagement, process standardization, and service excellence.
  • Develop and maintain standard operating procedures, project documentation, and operational workflows that help teams work consistently and effectively.
  • Prepare reports, presentations, and recommendations for leadership regarding project progress, risks, opportunities, and outcomes.
  • Serve as a primary liaison, when needed, between industry sponsors, investigators, subject matter experts, and institutional stakeholders.
  • Support and lead project meetings, sponsor discussions, site visits, and stakeholder working sessions, ensuring follow-up actions are completed.
  • Support the development and management of project scopes, budgets, proposals, statements of work, and sponsor deliverables.
  • Coordinate communication plans and provide regular project updates to leadership, sponsors, and stakeholders.
  • Perform other duties as assigned in support of the team and organizational goals.
  • Follow institutional policies, procedures, and regulatory requirements to support compliant research operations.

Benefits

  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials
  • Premiums
  • Bonuses as applicable
  • Recognition programs
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