Resources Global Professionals

Clinical Trials Manager

Resources Global Professionals$125K — $150K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA degree with 10+ years of experience in leading global clinical trials across multiple therapeutic areas.
  • Expertise in clinical development and regulatory compliance (FDA/EMA, ICH-GCP).
  • Experienced in mentoring and developing Clinical Operations teams.
  • Proven track record in CRO selection, negotiation, and management.
  • Strong financial acumen in budgeting and forecasting for clinical studies.

Responsibilities

  • Manage end-to-end clinical trial execution adhering to protocols and regulatory standards.
  • Oversee CROs and vendors from selection to performance evaluation.
  • Monitor study metrics, enrollment, timelines, and risk management to ensure trial success.
  • Collaborate with cross-functional teams to facilitate effective study execution.
  • Provide leadership in clinical documents, planning, and operational improvements.
  • Drive implementation of best practices and process enhancements in Clinical Operations.
  • Engage with investigators and vendors for both domestic and international study activities.

Benefits

  • Medical, Dental, and Vision insurance.
  • Life and Disability Insurance.
  • 401(k) Savings Plan.
  • Employee Stock Purchase Plan.
  • Professional Development Program.
  • Paid Time Off and Paid Sick Time.
Full Job Description
RGP is seeking a Clinical Trials Manager Consultant to lead the execution of clinical trials, ensuring compliance with protocols, SOPs, GCPs, and regulatory requirements. As the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial stewardship of clinical programs.

What You Will Work On

  • Manage end-to-end clinical trial execution, ensuring compliance with protocols, GCPs, SOPs, and regulatory standards.
  • Oversee CROs and vendors, including selection, contracting, budgeting, performance management, and issue escalation.
  • Monitor study metrics, enrollment progress, timelines, and risks to drive successful trial delivery.
  • Partner with Clinical Development, Regulatory, Legal, Finance, investigators, and key opinion leaders to support study execution.
  • Provide operational and technical leadership for clinical documents, trial planning, and process improvements.
  • Drive Clinical Operations best practices, functional initiatives, and continuous improvement efforts.
  • Support domestic and international study activities through regular site, investigator, and vendor engagement.


What You Will Bring

  • BS/BA degree with 10+ years of experience leading global, multi-site clinical trials across ophthalmology, neurology, rare disease, and drug development programs.
  • Expertise in clinical development, FDA/EMA regulations, ICH-GCP compliance, and global study execution.
  • Proven leadership of Clinical Operations teams, including direct management, mentoring, and staff development.
  • Extensive experience selecting, negotiating, and overseeing CROs and external vendors.
  • Strong financial acumen with responsibility for study budgets, forecasting, and financial reporting.
  • Effective collaborator with investigators, key opinion leaders, vendors, and executive stakeholders.


What You Can Expect

  • An inspirational place for you to do your best work, be engaged in meaningful ways, and continually develop the skills, competencies and qualities that set our team apart.
  • Compensation commensurate with your qualifications, experience, and other factors including geographic location, market and operational factors.
  • Total Rewards include: Medical, Dental, Vision, Life Insurance, Disability Insurance, 401(k) Savings Plan, Employee Stock Purchase Plan, Professional Development Program, Paid Time Off and Paid Sick Time (in geographies where legally required).

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