Senior Clinical Trial Manager – Remote

5+ years

Not Disclosed

Remote - South America (Latin Americal)

10 Feb. 12, 2025

Job Description

Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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: Senior Clinical Trial Manager – Remote

Location: Chile (Remote flexibility available for the right candidate)
Job Type: Full-time

ABOUT MEDPACE

Medpace is a leading full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our focus spans across multiple therapeutic areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, and anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals in more than 40 countries, with an expanding presence in South America.

JOB SUMMARY

Medpace is expanding its operations in South America and is seeking a Senior Clinical Trial Manager to join our Clinical Trial Management Group in Chile. This role is integral to the successful execution of clinical trials, ensuring compliance with ICH/GCP guidelines and regulations while overseeing various project aspects. Competitive salary/bonus programs and local benefits are offered for this role.

KEY RESPONSIBILITIES

Project Leadership & Oversight

Manage day-to-day operations of global clinical trials, ensuring compliance with the study protocol, ICH/GCP guidelines, and all applicable laws and regulations.
Serve as the primary sponsor contact for operational issues and deliverables throughout the study lifecycle.
Maintain thorough knowledge of the study protocol, therapeutic area, and indication to ensure appropriate trial management.
Oversee internal project teams, ensuring that all necessary project-specific training is provided to team members.
Review and provide input for the study protocol, edit check specifications, data analysis plans, and final study reports.
Develop operational project plans, manage project timelines, and track progress against goals.
Conduct risk assessments and manage their execution to mitigate issues during the project lifecycle.
Manage external study vendors, ensuring their deliverables align with study timelines and quality standards.
Ensure site quality by directly supervising monitoring deliverables and providing guidance to the team.

QUALIFICATIONS & EXPERIENCE

Education

Bachelor’s degree in a health-related field required.
Advanced degree (Master’s or PhD) in a health-related field is preferred.

Experience

A minimum of 5 years of experience as a Project/Clinical Trial Manager within a CRO.
Experience in managing clinical trials in Phases 1-4, with a preference for Phases 2-3 experience.
Proven track record in managing project timelines and deliverables in a global setting.
Bid defense experience is preferred but not mandatory.

Skills & Competencies

Strong leadership and project management skills, with a focus on team coordination and delivery.
Excellent communication skills, both written and verbal, with the ability to manage stakeholder expectations.
Ability to adapt to changing priorities and manage multiple projects simultaneously.
A strong understanding of regulatory requirements and clinical trial standards (ICH/GCP).

COMPENSATION & BENEFITS

Competitive salary/bonus program.
Local benefits tailored to the Chilean market.
Flexible work environment, with remote options available for the right candidate.
Paid time off (PTO), starting at 20+ days.
Employee health and wellness initiatives.
Company-sponsored employee appreciation events and recognition programs.
Discounts for local businesses.

AWARDS & RECOGNITION

Forbes: Recognized as one of America's Most Successful Midsize Companies (2021, 2022, 2023, and 2024).
CRO Leadership Awards from Life Science Leader magazine for excellence in expertise, quality, capabilities, reliability, and compatibility.

WHY MEDPACE?

At Medpace, we are driven by a shared mission to improve the lives of patients through the development of innovative therapeutics. By joining our Clinical Trial Management team, you'll be part of an organization that is making a real impact on global health.

HOW TO APPLY

Apply now to join Medpace's growing presence in South America and lead the way in successful global clinical trials!

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