Precision Medicine Group

Senior Project Manager, Clinical Trials

Precision Medicine Group

full-time

Posted on:

Location Type: Remote

Location: Remote • 🇸🇰 Slovakia

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Job Level

Senior

Tech Stack

Google Cloud Platform

About the role

  • You will independently lead clinical projects in accordance with the study budget and scope of work.
  • Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations
  • Liaise with Project Team and senior management of both Precision and sponsors, including C level
  • Handle and lead all aspects of a clinical research trial or trials
  • Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
  • Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
  • Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
  • Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets

Requirements

  • Degree or similar related life science qualification, or equivalent combination of education and experience.
  • Previous experience in a full service/global Project Management role working in the CRO industry is essential.
  • 5 to 7 years industry experience and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
  • Experience managing studies within Oncology
  • Working understanding of GCP/ICH guidelines and the clinical development process
  • Ability to drive and availability for domestic and international travel including overnight stays
  • Be able to communicate effectively in the English language both written and spoken
  • Strong presentation skills
  • Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
  • Proven ability to develop positive working relationships with individual and teams internally and externally
  • Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan.
Benefits
  • We offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments.
  • We are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development.

Applicant Tracking System Keywords

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

Hard skills
project managementclinical researchdata managementbiostatisticsmedical monitoringprotocol preparationperformance metricsclinical development processOncology studiesGCP/ICH guidelines
Soft skills
customer servicecommunicationpresentation skillsrelationship buildingteam collaborationleadershiporganizational skillsproblem-solvingtime managementadaptability