Instagram
youtube
Facebook

Clinical Trial Manager - Denver, Co

5+ years
$100,000 - $190,000
10 Nov. 26, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 is seeking established Project Managers to join their Clinical Trial Management Group in Denver, CO. As a leading Contract Research Organization (CRO) for biotech companies, Medpace offers an exciting opportunity to work across therapeutic areas such as Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. The company also provides flexibility for remote work based on relevant experience. Competitive salary, bonus programs, and equity grants are offered to associates.

Responsibilities

  • Project Management: Oversee day-to-day operations of clinical trials, ensuring compliance with contracts, ICH/GCP, and applicable regulations.
  • Sponsor Communication: Serve as the primary contact for Sponsors on operational project-specific issues and deliverables.
  • Study Oversight: Maintain in-depth knowledge of study protocol, therapeutic area, and indications. Provide oversight of internal project teams and ensure necessary training.
  • Study Documents: Provide input on study protocols, edit check specifications, data analysis plans, and final study reports.
  • Risk Management: Lead operational project planning, risk assessment, and execution.
  • Vendor and Site Management: Supervise study vendors, clinical research associates, and site quality.

Qualifications

  • Education: Bachelor’s degree in a health-related field; advanced degree preferred.
  • Experience: 5+ years as a project/clinical trial manager within a CRO. Experience managing Phases 1-4 studies, with a preference for Phases 2-3.
  • Skills: Strong leadership and project management skills with the ability to manage overall project timelines.

Compensation

  • Target Salary Range: $100,000 - $190,000 per year, based on experience.
  • Benefits: Includes medical, dental, vision, 401(k), PTO, paid holidays, short-term and long-term disability, flexible savings accounts, life insurance, and pet insurance.

Medpace Overview

Medpace is a full-service CRO providing Phase I-IV clinical development services to the biotech, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.

Why Medpace?

  • Impactful Work: Medpace's work helps improve the lives of patients battling various diseases.
  • Perks: Flexible work environment, competitive PTO, career growth opportunities, employee wellness initiatives, and discounts on local services.
  • Awards: Recognized as a Top Workplace in 2024 and named among America’s Most Successful Midsize Companies (2021-2024).

What to Expect Next

Medpace will review your qualifications and contact you if you're a good fit for the role.