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Senior Clinical Research Project / Trial Manager

Saratoga Ascend United States

7 h ago
Remote Principal (10+ yrs) Full-time United States
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About the role

The manager will oversee multi-site clinical trials from start-up through close-out while managing contract deliverables, budgets, and risks. They will also coordinate clinical operations, regulatory functions, and quality assurance while leading multidisciplinary teams.

What they look for

Clinical research Project management Trial management NIH-regulated studies FDA-regulated studies Clinical operations Data management Regulatory compliance Quality assurance Stakeholder communication Gene therapy Rare disease studies Good clinical practice ICH E6 HIPAA Multidisciplinary team leadership

Requirements

Candidates must have at least 8 years of clinical research experience, including 5 years managing NIH or FDA-regulated programs. A bachelor's degree in a life science field is required, with preference given to those holding a master's degree or professional certifications like PMP or CCRP.

Benefits

Competitive rate Benefit options

Full description

Saratoga Medical is hiring a Remote, Senior Clinical Research Project / Trial Manager. Package includes competitive rate and benefit options. Please see qualifications below and submit your resume if you are interested in being considered:

Education: Bachelor's degree in life sciences, nursing, public health or a related field required; master's degree or PMP/CCRP/ACRP-CP certification preferred.

Experience: Minimum of 8 years of clinical research experience, including at least 5 years managing NIH- or FDA-regulated studies and leading multidisciplinary teams.

Qualifications:

  • Demonstrated oversight of multi-site or complex clinical trials from start-up through close-out
  • Experience managing task-order or contract deliverables, schedules, budgets and risks
  • Proven ability to coordinate clinical operations, monitoring, data management, regulatory and quality functions
  • Experience with quality assurance oversight, corrective action tracking, and staffing and transition planning
  • Strong leadership, stakeholder communication and Government reporting skills
  • Experience with gene therapy or rare disease studies is advantageous
  • Five or more years of direct experience supporting NIH or FDA-regulated clinical research programs
  • Working knowledge of Good Clinical Practice (ICH E6), 21 CFR Parts 11, 50, 54, 56, 312 and 812 (as applicable), 45 CFR Part 46, and HIPAA
  • Current human subjects protections and GCP training (e.g., CITI or equivalent)
  • Experience working in a multidisciplinary team environment alongside Government clinical investigators, regulatory staff and program officials

Saratoga Medical Center, Inc. is an equal opportunity employer and will not discriminate in recruiting, hiring, training, promotion, transfer, discharge, compensation or any other term or condition of employment on the basis of race, religion, color, age (over age 39), sex, national origin, or on the basis of disability if the employee can perform the essential functions of the job, with a reasonable accommodation if necessary.