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Senior Project Manager - Clinical Trials - Project Management

7+ years
$125,200—$187,800 USD
10 July 7, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Project Manager – Clinical Trials (Project Management)
Location: Remote, United States
Job Type: Regular Full-time
Division: Precision for Medicine – Clinical Solutions
Requisition Number: 5771
Estimated Salary Range: $125,200 – $187,800 USD
Bonus Eligibility: Yes (discretionary annual bonus)


Position Overview:
Precision for Medicine is seeking a Senior Project Manager to lead and manage clinical trial projects with precision and agility. In this pivotal role, you’ll coordinate functional services and external vendors, manage budgets, ensure regulatory compliance, and serve as the primary client liaison—all while helping deliver cutting-edge therapies. This role requires exceptional leadership and project execution skills in a global, cross-functional environment.


Key Responsibilities:

  • Serve as primary client point-of-contact and escalation lead

  • Coordinate cross-functional teams and external vendors to meet project timelines and budgets

  • Manage study budgets and identify out-of-scope activities proactively

  • Oversee project profitability, billing, and forecasting

  • Develop and implement comprehensive project plans with risk mitigation strategies

  • Ensure inspection readiness, quality control, and resolution of deviations or incidents

  • Lead project meetings with internal stakeholders and clients

  • Provide regular project updates and KPI reports to senior leadership

  • Conduct formal presentations, including Bid Defenses

  • Oversee and maintain eTMF, EDC, CTMS, and related systems

  • Support business development initiatives as needed

  • Supervise and provide feedback to functional team members


Qualifications:

Minimum Requirements:

  • Bachelor’s degree in a science or health-related field (Master’s preferred)

  • 7+ years of clinical research experience, with at least 4 years in project management

  • Experience managing complex, global trials

  • Strong working knowledge of ICH-GCP, SOPs, Microsoft Project, eTMF, EDC, CTMS

  • Strong interpersonal, analytical, and leadership skills

  • Excellent communication and stakeholder management

  • Willingness to travel domestically/internationally as required

Preferred:

  • Experience in oncology or cell and gene therapy trials

  • Advanced project management training or certification

  • Demonstrated success in cross-functional team leadership


Additional Information:

  • #LI-Remote

  • Benefits include: Health insurance, 401(k) with matching, parental leave, vacation/sick leave, life/disability coverage, and more