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Senior Clinical Trial Manager - Oncology

Worldwide Clinical Trials

Any City, NCRemotePosted 41 days ago$112,000.00 - $222,000.00/year
Full TimeSenior LevelClinical DevelopmentCRO
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Summary

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

Job description

What Clinical Operations Site Management does at Worldwide

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

What you will do

  • Provide leadership and direction to clinical site management team members from study start through to closure
  • Serve as Site Management's primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to
  • Primary Sponsor Contact
  • Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English
  • Ability to lead and motivate a team remotely
  • Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified
  • Strong customer focus, ability to interact professionally with a sponsor contact
  • Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

  • Bachelor's Degree or a Nursing Degree required
  • 2+ years' experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
  • 4+ years' experience as a Clinical Research Associate
  • Oncology experience is required
  • Willingness to travel up to 30%

Requirements

  • Bachelor's Degree or a Nursing Degree required
  • 2+ years' experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
  • 4+ years' experience as a Clinical Research Associate
  • Oncology experience is required
  • Willingness to travel up to 30%
  • Excellent interpersonal, oral, and written communication skills in English
  • Ability to lead and motivate a team remotely
  • Demonstrate initiative and problem-solving skills
  • Strong customer focus
  • Proficiency in Microsoft Office, CTMS, and EDC Systems

Benefits

  • Competitive benefits package

Company overview

Worldwide Clinical Trials is a leading global contract research organization (CRO) that provides comprehensive clinical development services to pharmaceutical, biotechnology, and medical device companies. Founded with a mission to accelerate the development of innovative therapies, the company offers end-to-end solutions spanning from early-phase research through late-stage clinical trials and regulatory submissions. With expertise across multiple therapeutic areas including oncology, central nervous system disorders, cardiovascular diseases, and rare conditions, Worldwide Clinical Trials leverages its scientific knowledge and operational excellence to design and execute complex clinical studies. The organization maintains a global footprint with operations across North America, Europe, and Asia-Pacific regions, enabling it to conduct multinational trials efficiently. Known for its patient-centric approach and commitment to quality, Worldwide Clinical Trials plays a crucial role in advancing medical research and bringing new treatments to patients worldwide.

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