Skip to main content
ResumeKart
← Back to Jobs

Clinical Team Manager / Sr. (CTM) - HemOnc

Lifelancer•United States•🌍 Remote
Full-timeSenior
👁️ 0 views•📝 0 applications•Posted 9/20/2026•Expires 11/19/2026
Tailor Resume for This JobCheck ATS Score

Get alerts for roles like this

More Clinical Team Manager / Sr. (CTM) - HemOnc roles in United States — straight to your inbox. No account needed.

Applying to this role? Tailor your résumé to this job description in one click, then download it free — just a small ResumeKart footer, no subscription.

Job Description

Job Title: Clinical Team Manager / Sr.

(CTM) - HemOnc Job Location: Remote, North Carolina, USA Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer.

The Clinical Trial Manager interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations.

Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. The position involves working on projects of low to moderate complexity and as part of a team of CTMs.

What You'll Do

• Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.

• Develop clinical tools (e. g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents.

Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required.

Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meeting

Required Skills

ICH GCPClinical Study ManagerMonitoring PlanMonitoring GuidelinesTrial Master FileCRFspatient informed consent

Partner picks for Clinical Team Manager / Sr. (CTM) - HemOnc in United States

Matched to the skills this page calls for and the candidate's location.

Partner
  • edXVerified partner
    Partner course provider

    Courses and programmes from universities and institutions worldwide.

  • Partner course provider

    University and industry courses, professional certificates and online degrees.

  • Partner course provider

    Certification training in cloud, data, cyber security, project management and digital marketing.

Partners are ResumeKart affiliates or institutes it works with; ResumeKart may earn a commission when a candidate enrols. Placement is decided by relevance, not payment. How ResumeKart earns

The best-paying roles in your field. Every week. Free.

Get job alerts and salary insights in your inbox

We respect your privacy. Unsubscribe anytime with one click.