Clinical Trial Manager (Cardiovascular/Renal/Metabolic/Gastrointestinal) at Medpace, Inc.

South Yarra, Victoria, Australia -

Full Time

Start Date

Immediate

Expiry Date

08 Apr, 26

Salary

0.0

Posted On

08 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Management, Cardiovascular Studies, Renal Studies, Metabolic Studies, Gastrointestinal Studies, Project Management, Risk Assessment, Communication Skills, Protocol Knowledge, Team Oversight, Vendor Management, Quality Management, Data Analysis, Training, Regulatory Compliance, Operational Planning

Industry

Pharmaceutical Manufacturing

Description

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Melbourne, Australia. Clinical Trial Managers with expertise in Cardiovascular, Renal, Metabolic or Gastrointestinal related are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Responsibilities Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations; Serve as primary Sponsor contact for operational project-specific issues and study deliverables; Maintain in depth knowledge of protocol, therapeutic area, and indication; Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided; Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable; Develop operational project plans; Manage risk assessment and execution; Responsible for management of study vendor; and Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables. Qualifications Bachelor’s degree in a health or life science-related field; At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment; Experience in Cardiovascular, Renal, Metabolic or Gastrointestinal related studies required; Excellent communication skills including good written and spoken English; and Flexible, accountable and comfortable in working in a global environment. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Responsibilities

The Clinical Trial Manager will manage day-to-day operations of clinical projects, ensuring compliance with ICH/GCP and other regulations. They will serve as the primary contact for sponsors and oversee internal project teams and deliverables.