Precision Medicine Group

Clinical Trial Manager

Precision Medicine Group

full-time

Posted on:

Location Type: Remote

Location: Remote • 🇭🇺 Hungary

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Job Level

Mid-LevelSenior

Tech Stack

Google Cloud Platform

About the role

  • Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
  • Successful execution of assigned trials and ensuring completion of trial deliverables
  • Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members
  • Mentoring and training of team members
  • Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
  • Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
  • Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction
  • Act as hub of central intelligence for studies, leading CRAs and overseeing all clinical aspects across multiple countries, ensuring timeline adherence, scope, and quality delivery

Requirements

  • Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology
  • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role)
  • Significant clinical trial management experience in the area of oncology
  • Working knowledge of GCP/ICH guidelines and the clinical development process
  • Availability for domestic and international travel including overnight stays
  • Must be able to communicate effectively in the English language
  • Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
  • Demonstrated ability to develop positive working relationships with internal and external organizations
  • Core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
  • Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
clinical trial managementoncologyGCPICH guidelinesclinical development processdata cleaningmonitoring planningenrolment managementsite selectionregulatory documentation
Soft skills
communicationmentoringteam leadershipproblem-solvingrelationship buildingcross-functional collaborationclient satisfactioncreative action planningoversightfocus on priorities
Precision Medicine Group

Senior Feasibility Associate / Feasibility Manager

Precision Medicine Group
Seniorfull-time🇭🇺 Hungary
Posted: 2 hours agoSource: boards.greenhouse.io
Google Cloud Platform