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Sr. Clinical Trial Manager

  • Company: Get A Job.ai
  • Location: United States
  • Salary: Pay not listed

Website Get A Job.ai

Represented by Get A Job.ai

About This Opportunity

Our talent team at Get A Job.ai is representing a confidential radiopharmaceutical biotechnology organization in their search for a Sr. Clinical Trial Manager. This role offers the opportunity to contribute to innovative oncology programs while managing clinical studies from Phase I through Phase III. You'll work with a multidisciplinary team focused on developing transformative therapies for patients with cancer.

Responsibilities

  • Lead the planning, execution, and closeout of clinical trials across all phases
  • Oversee and manage Clinical Research Organizations (CROs) and vendors to ensure studies are completed on time, within budget, and in full compliance with SOPs, FDA regulations, and ICH/GCP guidelines
  • Lead cross-functional study execution teams in achieving study goals and deliverables
  • Plan and execute study timelines while monitoring progress including enrollment, site performance, data quality, and key risk indicators
  • Proactively identify, assess, and mitigate operational risks, escalating issues to internal stakeholders as needed
  • Manage study budgets and invoicing procedures according to contract terms
  • Lead and support country and site feasibility, selection, and activation strategies
  • Participate actively in CRO and vendor meetings, reviewing operational plans and providing strategic input
  • Summarize performance data and escalate study risks to program leadership
  • Travel up to 20% as required

What We're Looking For

  • Minimum 5-7 years of clinical operations experience within biotech, pharmaceutical, or CRO environments
  • BA/BS degree; scientific or healthcare discipline preferred
  • Independent professional who communicates proactively, frequently, and effectively
  • Detail-oriented and action-focused with strong organizational skills and commitment to quality
  • Proven ability to work successfully in cross-functional teams
  • Comfortable working in dynamic environments with a high degree of flexibility
  • Expertise in Microsoft Project and Smartsheets desired
  • Experience applying AI tools to improve team execution and decision-making

How We Work with You

When you apply through Get A Job.ai, one of our recruiters will screen your qualifications and present strong matches to our client. If selected to move forward, we will coordinate your interview process. Please do not contact the hiring organization directly—all communication should flow through our team to ensure a smooth and professional experience.

Location and Work Environment

This is a remote position based in the United States. The work environment is typically moderate in noise level.

Equal Employment Opportunity

Get A Job.ai is committed to equal employment opportunity. We consider all qualified applicants regardless of race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Apply with Get A Job.ai

A recruiter will review your profile and submit you to the client. Do not contact the client directly.

More options

Apply with Get A Job.ai

Apply through Get A Job.ai. A recruiter will review your profile and submit you. Do not contact the client directly.

Apply through Get A Job.ai. A recruiter will review your profile and submit you.

Local insights for this role are preparing — this section updates automatically in a few seconds (or refresh).

Listing facts

  • Role Sr. Clinical Trial Manager
  • Employer Get A Job.ai
  • Location United States
  • Type Full Time
  • Pay (from listing) Pay not listed
  • Posted September 13, 2026
  • Apply by October 13, 2026
  • Country United States
  • Overview Full job description on this page (401 words)

Facts above come from this job record on Get A Job.AI — not copied from third-party review sites.

Typical work in Clinical Trial Manager

Independent occupational context from O*NET (U.S. public-domain labor data). This is about the occupation, not a rewrite of this employer's posting.

  • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Inform patients or caregivers about study aspects and outcomes to be expected.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

Source: O*NET

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Sr. Clinical Trial Manager Get A Job.ai · United States