Program Manager

Spectrum Staffing, Inc.; Denville (NJ); A distancia; USD 112.000 - 156.000; A tiempo parcial

Ventajas ofrecidas por este puesto de trabajo

Remote work

Six-month contract

Descripción de la vacante

Spectrum Staffing, Inc. seeks an experienced Program Data Manager to oversee complex clinical data management initiatives across multiple studies and global teams. This remote, six-month assignment enables you to lead cross-functional programs, guide data strategies, and contribute to regulatory submissions.

You will align data collection with CDISC SDTM, mentor colleagues, and build relationships across functions in a matrixed environment while working independently in a collaborative setting.

Formación

• Advanced experience leading complex studies or programs.
• Strong understanding of clinical data collection strategies and CDISC SDTM.
• Familiarity with health authority submission support and documentation.
• Ability to lead global, cross-functional teams and influence stakeholders without direct reporting authority.

Responsabilidades

• Lead multiple clinical studies and data management workstreams across international teams.
• Define program objectives, scope, milestones, and deliverables for timely execution.
• Act as primary contact for health authority submission activities and regulatory meetings when needed.
• Shape data collection approaches in line with CDISC SDTM and industry standards.
• Design and deliver operational and therapeutic-area training for internal and external teams.
• Provide senior-level technical guidance across related functions and processes.
• Mentor colleagues and represent data management leadership in a matrixed environment.

Conocimientos

Leadership

CDISC SDTM

Regulatory submissions

Global teams

Educación

Advanced degree in life sciences

Descripción del empleo

Seeking an experienced Program Data Manager to oversee complex clinical data management initiatives across multiple studies and global teams. This remote, six-month assignment offers the opportunity to lead cross-functional programs, guide clinical data strategies, and contribute to regulatory submission activities while working independently in a highly collaborative environment.

RESPONSIBILITIES

• Lead multiple clinical studies and complex data management workstreams, coordinating priorities across international, cross-functional teams.
• Define program objectives, project scope, milestones, and deliverables to support timely and effective execution.
• Act as a primary contact for health authority submission activities, including briefing materials and participation in regulatory meetings when needed.
• Help shape clinical data collection approaches in alignment with applicable standards, including CDISC SDTM.
• Design and deliver operational and therapeutic-area training for internal colleagues and external study teams.
• Provide subject matter expertise, technical guidance, and practical solutions across related functions and processes.
• Build productive relationships with stakeholders, influence decisions, and encourage strong team performance in a matrixed environment.
• Mentor colleagues, share effective practices, and represent clinical data management leadership when requested.

QUALIFICATIONS

• Advanced experience in clinical data management, including leadership of complex studies or programs.
• Strong understanding of clinical data collection strategies and relevant standards, including CDISC SDTM.
• Familiarity with health authority submission support and associated documentation.
• Proven ability to lead global, cross-functional teams and influence stakeholders without direct reporting authority.
• Ability to manage parallel priorities, make independent decisions, and provide senior-level technical guidance.
• Effective communication, training, mentoring, and stakeholder coordination skills.

BENEFITS

• Remote work arrangement with the flexibility to collaborate across global teams.
• Opportunity to contribute to complex, high-impact clinical programs during a six-month assignment.
• Broaden experience in regulatory submission support, clinical data strategy, and international program delivery.
• Build leadership and technical expertise while partnering with experienced, multidisciplinary professionals.