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Associate Clinical Trial Manager - Phd / Post-Doc Experience - Denver, Co

2+ years
$70,000 - $90,000
10 Nov. 26, 2024
Job Description
Job Type: Full Time Education: MSc./M. Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Summary

Medpace, a leading Contract Research Organization (CRO) for Biotech companies, is seeking a full-time Associate Clinical Trial Manager (aCTM) for their Clinical Trial Management team in Denver, CO. This role is ideal for recent PhD graduates or individuals with post-doctoral research experience looking to transition into clinical project management. The aCTM will work alongside Project Coordinators and Clinical Trial Managers to support various project management activities. This position offers a unique opportunity for career growth, including an intensive training period and a fast-track path into Clinical Trial Management (CTM).

Responsibilities

  • Collaboration: Work closely with Project Coordinators and Clinical Trial Managers to support global study activities.
  • Task Management: Ensure the timely and accurate delivery of recurrent tasks.
  • Project Reporting: Compile and maintain project-specific status reports in the clinical trial management system.
  • Communication: Interact with internal teams, Sponsors, study sites, and third-party vendors.
  • Regulatory Oversight: Provide oversight and quality control of internal regulatory filing systems.
  • Study Supplies: Manage and oversee study supplies.
  • Project Timelines: Create and maintain detailed project timelines.
  • Meeting Coordination: Organize and facilitate project meetings and ensure quality meeting minutes.

Qualifications

  • Education: PhD in Life Sciences.
  • Language Skills: Fluency in English with strong presentation abilities.
  • Teamwork: Ability to thrive in a fast-paced, dynamic, international team environment.
  • Industry Experience: Prior experience in a CRO or pharmaceutical setting is beneficial but not required.
  • Technical Skills: Proficiency in Microsoft Office (Word, Excel, PowerPoint), databases, and excellent organizational and communication skills.

Compensation

  • Target Salary Range: $70,000 - $90,000, based on skills and experience.
  • Benefits: Includes medical, dental, vision, 401(k), PTO, sick days, paid holidays, short-term and long-term disability, health savings and flexible savings accounts, life insurance, and pet insurance.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO), providing Phase I-IV clinical development services to the biotech, pharmaceutical, and medical device industries. Their mission is to accelerate the development of safe and effective medical therapeutics through a scientific and disciplined approach. They operate globally, employing more than 5,000 people in over 40 countries.

Why Medpace?

  • Impact: Medpace has made a positive impact on patients and families globally, particularly across oncology, cardiology, metabolic diseases, CNS, and anti-infective areas.
  • Growth and Development: Structured career paths and professional growth opportunities.
  • Perks: Flexible work environment, competitive PTO, employee wellness initiatives, and local discounts (sports, fitness, attractions).
  • Awards: Recognized as a Top Workplace in 2024 and one of America's Most Successful Midsize Companies (2021-2024).

What to Expect Next

Medpace will review your qualifications and, if you are a good fit, you will be contacted with the next steps in the hiring process.