Associate Clinical Trial Manager

Medpace Clinical Research India Pvt. Ltd.

2+ years

Preffered by Company

Remote, USA

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: Associate Clinical Trial Manager (aCTM)
Location: Melbourne, Australia

Company Overview:

Medpace is a leading Contract Research Organization (CRO) that provides comprehensive Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With over 5,000 employees across 40+ countries, we are dedicated to accelerating the global development of safe and effective medical therapeutics through a scientific and disciplined approach. Our expertise spans various therapeutic areas, including oncology, cardiology, and central nervous system disorders. Headquartered in Cincinnati, Ohio, Medpace is recognized for its excellence and commitment to advancing medical research.

Role Summary:

We are seeking a dedicated Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Melbourne. This role is ideal for recent PhD graduates or individuals with Post-Doctoral research experience who are eager to transition into clinical project management. The aCTM will support Project Coordinators and Clinical Trial Managers in overseeing and executing project management tasks. This position offers a unique opportunity to apply analytical and academic skills to clinical project administration and management.

Responsibilities:

Global Study Coordination: Collaborate on global study activities, working closely with the Project Coordinator and Clinical Trial Manager.
Task Management: Ensure the timely completion of recurring tasks with high accuracy.
Project Reporting: Compile and maintain project-specific status reports within the clinical trial management system.
Stakeholder Interaction: Engage with internal project teams, Sponsors, study sites, and third-party vendors.
Regulatory Oversight: Provide quality control for our internal regulatory filing system.
Study Supplies Management: Oversee and manage study supplies.
Timeline Management: Create and maintain project timelines.
Meeting Coordination: Coordinate project meetings and produce detailed minutes.

Qualifications:

Education: PhD in Life Sciences.
Experience: Experience in oncology preferred.
Language Skills: Fluency in English with strong presentation skills.
Industry Knowledge: Ability to thrive in a fast-paced, international team environment. Prior experience in a CRO or pharmaceutical industry is advantageous but not required.
Technical Skills: Proficiency in computer applications (word processing, databases, Excel, Windows), with excellent organizational and communication skills.

Why Medpace?

At Medpace, we are committed to making a difference by advancing medical research and improving patient outcomes. Our work has positively impacted countless lives, and we strive to continue this legacy of excellence and innovation.

Medpace Perks:

Hybrid Work Options: Flexibility to work from home (dependent on position and level).
Competitive PTO: Generous paid time off packages.
Employee Appreciation: Company-sponsored events and health and wellness initiatives.
Flexible Schedule: Opportunities for flexible work hours.
Compensation & Benefits: Competitive salary and benefits package.
Career Growth: Structured career paths and opportunities for professional development.

Awards and Recognition:

Forbes Recognition: Named one of America's Most Successful Midsize Companies (2021, 2022, 2023, 2024).
CRO Leadership Awards: Continually recognized for expertise, quality, capabilities, reliability, and compatibility by Life Science Leader magazine.

Join Us:

If you are passionate about contributing to the advancement of clinical research and are eager to start a career in Clinical Trial Management, apply today to join Medpace and be part of our mission to shape the future of healthcare.

Apply Now and make a difference with Medpace.

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Associate Clinical Trial Manager

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