Research Program Leader

Duke Careers

. Support clinical research for Hematologic Malignancy and Cell Therapies Clinical Research Teams .

Posted 9/21/2026full-timeRemote • North Carolina • United StatesSenior💰 $78,347 - $133,188 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research projects, including data management, compliance with regulations, and operational strategy development. Proficient in coordinating with study teams, sponsors, and CROs while ensuring effective communication and stakeholder engagement.

Highest-signal resume keywords

Clinical Research ManagementRegulatory ComplianceData ManagementProject CoordinationStakeholder Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Research Data ManagementClinical Trial ProtocolsSOP DevelopmentProgram EvaluationBudget ManagementRecruitment StrategiesOperational PlanningAudit TrainingProposal DevelopmentManuscript Editing

Soft Skills

Team LeadershipMentoringProblem SolvingCommunicationCollaboration

Certifications & Qualifications

Duke Specific TrainingClinical Research Certification

Industry Keywords

Hematologic MalignancyCell TherapiesEthical GuidelinesClinical Research PoliciesStudy Population InteractionVulnerable Research PopulationsResearch Program GoalsSite VisitsStakeholder FeedbackPerformance Improvement

About the role

Key responsibilities & impact

Support clinical research for Hematologic Malignancy and Cell Therapies Clinical Research Teams
Perform research, data, administrative, and coordination duties
Collect, compile, document, and manage clinical research data
Coordinate agreements with study teams and Duke offices
Serve as an expert resource on regulatory and institutional policies and processes
Lead or participate in monitoring and audit training sessions and develop policies and guidelines
Develop and oversee recruitment, retention, SOP, documentation, and operational strategies
Prepare for, coordinate, and participate in site visits
Communicate with sponsors and CROs
Manage protocol systems, reports, resources, and operational plans across study teams or sites
Determine research program goals, gaps, constraints, needs, and milestones with investigators
Manage the research project lifecycle from initiation through closing
Direct project staff and adjust plans and timelines based on stakeholder feedback
Manage program operations, budgets, staff mentoring, and training
Ensure compliance with relevant regulations and policies
Provide guidance on recruitment, consenting, study documentation, program evaluation, and data capture
Develop and edit research proposals and manuscripts
Represent the research program on behalf of the PI at internal and external meetings
Communicate with study personnel and resolve routine protocol issues
Seek technical knowledge and contribute to innovation and performance improvement
Participate in committees and workgroups
Establish and assign team activities to accomplish study goals

Requirements

What you’ll need

Completion of a Bachelor's degree
Minimum of four years of research experience, such as research, clinical, interaction with study population, or program coordination
Master's degree may substitute for two years of related experience
Maintain Duke and project specific training and certification requirements
Knowledge of regulations, policies, resources, and ethical guidelines relevant to clinical research
Ability to understand and follow policies, SOPs, regulations, and protocol requirements governing clinical research
Ability to identify and explain clinical trial risks and benefits
Ability to safeguard vulnerable research populations
Advanced subject matter expertise in the therapeutic area or clinical research
Ability to navigate Duke clinical research processes and organizational structures

Benefits

Comp & perks

Comprehensive medical and dental care programs
Generous retirement benefits
Family-friendly and cultural programs