Senior Clinical Project Manager: Lead Trials & CROs

Tonix Pharmaceuticals; Berkeley Heights (NJ); On-site; USD 115,000 - 167,000; Full time

Benefits offered by this job

Medical Insurance

401k with match

Generous PTO

Job summary

Tonix Pharmaceuticals seeks a Senior Clinical Project Manager to oversee trials across clinical programs, manage CROs, and ensure studies are delivered on time, on budget, and within scope. You will partner with other functional areas to drive program success.

Responsibilities include protocol development, vendor management, budgets, site coordination, and regulatory considerations, with up to 25% travel. Candidates should have 8+ years in clinical operations and solid GCP knowledge.

Qualifications

• Bachelor's degree in life sciences or related field.
• Advanced degree highly desirable.
• Minimum 8 years in clinical operations or research with increasing levels of responsibility.
• Minimum 4 years managing clinical projects, ideally from start to end of a trial.
• Detail oriented and organized with strong communication skills.

Responsibilities

• Assist with protocol and informed consent development.
• Master elements of study protocol and materials.
• Evaluate CROs and vendors in a structured fashion.
• Negotiate budgets and contracts; communicate with third party vendors.
• Lead regular project meetings; track minutes and actions.
• Manage vendor budgets, invoices/payments, and timelines.

Skills

Communication skills

ICH GCP knowledge

Project management

Microsoft Office (Office 365/SharePont

Team mentoring

Travel up to 25%

Education

Bachelor's degree in life sciences

Advanced degree desirable

Tools

EDC

TMF

CTMS

IRT systems

Job description

Tonix Pharmaceuticals seeks a Senior Clinical Project Manager to oversee trials across clinical programs, manage CROs, and ensure studies are delivered on time, on budget, and within scope. You will partner with other functional areas to drive program success.

Responsibilities include protocol development, vendor management, budgets, site coordination, and regulatory considerations, with up to 25% travel. Candidates should have 8+ years in clinical operations and solid GCP knowledge.