Senior Clinical Project Manager (Chicago, IL)

senior

OtherClinical Project Manager

0 views0 saves0 applied

Apply Now

Quick Summary

Overview

function googleTranslateElementInit() { new google.translate.TranslateElement({pageLanguage: 'en'}, 'google_translate_element'); } Senior Clinical Project Manager (Chicago, IL)

Key Responsibilities

Contribute to our cutting-edge radiopharmaceutical development program Conceptualize, plan, design, place, execute, and summarize clinical trials Drive daily vendor and site management, including collaboration with Study Medical Monitor and KOLs to…

Requirements Summary

MINIMUM EXPERIENCE Biotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager 7+ years’ experience managing clinical trials including study design and…

Technical Tools

gcpproject-management

Responsibilities

~1 min read

→Contribute to our cutting-edge radiopharmaceutical development program
→Conceptualize, plan, design, place, execute, and summarize clinical trials
→Drive daily vendor and site management, including collaboration with Study Medical Monitor and KOLs to determine the medical and scientific needs
→Effectively communicate project-related information including the planning and execution of meetings and presentations as well as creation and maintenance of metrics, e.g., dashboards, timelines, resources, and budgets
→Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA)
→Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans
→Work in an office (Wilmette, IL north of Chicago) with a dynamic, talented team

Requirements

~2 min read

MINIMUM EXPERIENCE

Biotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager
7+ years’ experience managing clinical trials including study design and initiation, oversight, study closeout, project management, and regulatory filings
Demonstrated ability to plan and execute Pharma-Sponsored clinical trials, managing vendors and resources in effective & creative manners to achieve business needs including on-time, on-budget, and on-spec study results for successful use in regulatory marketing applications
Thorough knowledge of ICH-GCP, Food and Drug Administration (FDA), and European regulations
Excellent communication (oral and/or written), leadership, and risk mitigation skills plus a positive attitude
Require minimal guidance; is able to function in an independent manner
Proven ability to effectively manage internal and external personnel in clinical trial conduct

PREFERRED EXPERIENCE

9 years’ clinical trials experience in pharmaceutical or biotechnology firms
Experience in oncology trials
Experience managing clinical trials in Europe and/or Australia
Experience in a small or growth-stage biopharma company

Visit Careers at CEDENT

Subscribe to be notified of new jobs

If we don't have an open position that fits you, feel free to subscribe to our Talent Team email! Enter your name, email address and position(s) you're interested in, and whenever we open a new position matching your criteria we'll notify you immediately.