Associate Director, Clinical Trial Management – Remote

5+ years

Preffered by Company

Remote

10 Aug. 26, 2024

Job Description

Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/Any Life Sciences 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 Title: Clinical Trial Manager (CTM)
Location: Remote with flexibility (Experience required)

Company Overview:

Medpace is a leading Contract Research Organization (CRO) specializing in clinical development for the biotechnology, pharmaceutical, and medical device industries. With a focus on key therapeutic areas including Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, and Neuroscience, we are dedicated to accelerating the global development of safe and effective medical therapeutics. Headquartered in Cincinnati, Ohio, and with over 5,000 employees across more than 40 countries, Medpace is recognized for its commitment to scientific excellence and innovation.

Role Summary:

We are expanding our Clinical Trial Management Group and are seeking experienced Project Managers to join our team. This role offers the flexibility to work remotely, contingent upon relevant experience. The position comes with a highly competitive salary, bonus program, and equity grants that have proven to be very rewarding for our associates.

Responsibilities:

Project Management: Oversee day-to-day operations of clinical trials, ensuring adherence to contract terms, ICH/GCP guidelines, and all relevant regulations.
Sponsor Liaison: Act as the primary point of contact for operational issues and study deliverables with Sponsors.
Protocol Expertise: Maintain a comprehensive understanding of study protocols, therapeutic areas, and specific indications.
Team Oversight: Provide cross-functional oversight, ensuring project-specific training and effective coordination among internal project team members.
Study Documentation: Review and provide input on study protocols, edit check specifications, data analysis plans, and final study reports.
Project Planning: Develop and manage operational project plans, including risk assessment and mitigation strategies.
Vendor Management: Oversee and manage study vendors as applicable.
Quality Control: Ensure quality and compliance in site monitoring and deliverables.

Qualifications:

Education: Bachelor’s degree in a health-related field required; Advanced degree preferred.
Experience: Minimum of 5 years as a project/clinical trial manager within a CRO, with experience in Phases 1-4; Phases 2-3 preferred.
Skills: Proven ability to manage project timelines, with experience in bid defense preferred.
Leadership: Strong leadership and organizational skills required.

Why Medpace?

At Medpace, we are driven by a mission to make a difference through clinical research. Our work has positively impacted countless lives, and we are committed to improving future outcomes through innovative therapeutics.

Medpace Perks:

Hybrid Work Options: Flexibility to work from home, depending on position and experience level.
Competitive PTO: Generous paid time off, starting at 20+ days.
Employee Benefits: Health and wellness initiatives, company-sponsored appreciation events, and discounts for local businesses.
Career Development: Structured career paths, opportunities for professional growth, and flexible work schedules.
Awards: Recognized as a Top Workplace in 2024 by The Cincinnati Enquirer, and named one of America's Most Successful Midsize Companies by Forbes (2021-2024). Continually honored with CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility.

Join Us:

If you are an experienced Project Manager with a passion for clinical research and a desire to contribute to advancing medical science, we invite you to apply and become a part of our dynamic team at Medpace.

Apply Now and help us shape the future of clinical development.

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Associate Director, Clinical Trial Management – Remote

Job Description

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