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Medpace

Global CRO delivering full-service clinical trials

Clinical Trial Manager - Oncology

Full-TimeDeadline 1/8/27
No salary listed
Junior
Bachelor's, Master's, PhD
Melbourne VIC, Australia
HybridOffice-based, with occasional work from home for eligible positions after training.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A bachelor's degree in a health-related field is required; a master's degree or PhD is preferred.
  • At least 2 years of clinical trial management experience in the Asia Pacific region, ideally in a contract research organization environment.
  • Experience in oncology studies is required.
  • Excellent communication skills, including good written and spoken English.
  • Flexibility, accountability, and comfort working in a global environment.
Responsibilities
  • Manage and provide accountability for day-to-day project operations as defined by the contract and in accordance with ICH/GCP and applicable laws, rules, and regulations.
  • Serve as the primary Sponsor contact for operational project-specific issues and study deliverables.
  • Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
  • Provide cross-functional oversight of internal project team members and deliverables, including ensuring that all necessary project-specific training is provided.
  • Review and provide input for the study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
  • Develop operational project plans.
  • Manage risk assessment and execution.
  • Manage study vendors.
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
Desired Qualifications
  • A master's degree or PhD.
  • Clinical trial management experience in a contract research organization environment.

About the company

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device leaders. It runs Phase I–IV trials from study design through regulatory submissions, monitoring, data management, statistics, medical writing, and final reporting. A unique feature is ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—that streamline workflows and ensure data consistency. Its goal is to help sponsors bring therapies to market efficiently by coordinating all trial activities under a physician-led, scientifically driven team.

Company Size

5,001-10,000

Company Stage

IPO

Headquarters

Cincinnati, Ohio

Founded

1992

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Simplify's Take

What believers are saying

  • Q2 2026 revenue hit $707.3 million, up 17.2%, with 1.13x book-to-bill.
  • Medpace raised 2026 revenue guidance to $2.805 billion-$2.885 billion on July 23, 2026.
  • Zelluna chose Medpace on February 11, 2026 for its first-in-human TCR-NK trial.

What critics are saying

  • Durbin v. Medpace alleges February 2026 book-to-bill inflation; discovery runs through 2027.
  • Late-stage biotech funding freezes can stall clients, crushing backlog conversion within quarters.
  • If cancellations stay elevated, Medpace loses trust and full-service differentiation becomes commoditized.

What makes Medpace unique

  • August Troendle still runs Medpace with a physician-led, science-first operating model.
  • Medpace bundles CRO, central lab, bioanalytical, imaging, and ECG services in-house.
  • It specializes in small and mid-sized biotech sponsors needing full-service trial execution.

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Benefits

Flexible Work Hours

Unlimited Paid Time Off

Competitive Compensation and Benefits Package

Employee Health and Wellness Initiatives

Hybrid Work Options

Structured Career Paths with Opportunities for Professional Growth

Growth & Insights and Company News

Headcount

6 month growth

12%

1 year growth

12%

2 year growth

12%
Bionow
Sep 28th, 2026
Boyds expands Regulatory Affairs team to support growing demand.

Boyds expands Regulatory Affairs team to support growing demand. Expansion and Company Growth Staff News 28 Sep 2026 Global drug development consultancy Boyds has strengthened its award-winning Regulatory Affairs team with the appointment of two senior specialists, further expanding its ability to support life sciences companies as they navigate increasingly complex regulatory pathways. Established in 2005, Boyds works with an international client base to help translate scientific innovation into medicines and medical devices for patient benefit. Vicki Hayes joins Boyds as Vice President of Regulatory Affairs and Jan Ohotski joins as Director of Regulatory Affairs. Together, they bring senior expertise spanning global regulatory strategy, clinical development, small molecules, biotechnology therapeutics, and cell and gene therapies. Vicki brings more than 20 years' experience in regulatory affairs and joins Boyds from a US biotechnology company, where she was Vice President of Global Regulatory Affairs and Policy. She was previously a Board Director at a regulatory affairs consultancy, where she held several senior regulatory affairs roles, and has also worked at Amgen and Eli Lilly and Company. She has created and led regulatory strategies from first-in-human studies through to post-licensing across therapeutic areas including oncology, neuroscience, anti-infectives and rare diseases, and across modalities including small molecules, biologics and advanced therapies. In 2022, Vicki was awarded the TOPRA Regulatory Affairs Contribution Award. At Boyds, Vicki will lead the regulatory consulting function, working closely with clients to design robust, pragmatic regulatory strategies that support product development decisions. Commenting on her appointment, Vicki said: "Boyds thinks outside the box and provides a bespoke, tailored service that supports the development of novel, emerging and cutting-edge technologies. As Vice President of Regulatory Affairs, I look forward to developing creative and pragmatic regulatory strategies that accelerate development and maximise product value, as well as working with the award-winning Regulatory Affairs team, many of whom I have had the pleasure of working with previously." Jan joins Boyds from CRO Medpace, where he led the Cell and Gene Therapy team. He began his career as a scientist focused on drug discovery and pharmacology for oncological indications, working in both academia and industry, before moving into regulatory affairs more than ten years ago. He specialises in the clinical development of cell and gene therapies and, at Boyds, will support regulatory affairs activities alongside clinical operations. Jan commented: "Boyds is known in the industry for its impactful work on cutting-edge medicines, including cell and gene therapies. My interest in these therapies, along with my desire to further develop my expertise in regulatory consulting, attracted me to Boyds. I look forward to bringing practical operational knowledge across the non-clinical, clinical and CMC development of cell and gene therapies, including global expertise in biosafety risk assessments and associated submissions." Dr Katherine Bowen, Chief Regulatory Affairs Officer at Boyds, said: "We are delighted to welcome Vicki and Jan to Boyds. Their combined experience further strengthens our ability to provide strategic and practical regulatory support to clients developing innovative medicinal products. "Demand is rising as clients face complex regulatory challenges and need expert support to keep programmes moving efficiently. Our Regulatory Affairs team has built long-standing, trusted relationships with leading regulators, founded on decades of regulatory experience and constructive engagement. The appointment of Vicki and Jan further solidifies these relationships, enabling productive, solution-focused discussions that help clients anticipate requirements, address regulatory questions and move development programmes forward."

American Market News
Sep 3rd, 2026
Hsbc Holdings PLC Makes New Investment in Medpace Holdings, Inc. $MEDP

Hsbc Holdings PLC bought a new position in Medpace Holdings, Inc. (NASDAQ:MEDP – Free Report) in the 2nd quarter, according to the company in its most recent 13F filing with the Securities and Exchange Commission. The firm bought 977 shares of the company’s stock, valued at approximately $518,000. Several other hedge funds and other institutional […]

Yahoo Finance
Aug 17th, 2026
Medpace leads drug development services sector with $707M Q2 revenue, up 17.2% year-on-year

Medpace reported revenues of $707.3 million in Q2, up 17.2% year on year, exceeding analyst expectations by 2.6%. The contract research organisation, which provides outsourced clinical trial management services to pharmaceutical and biotech companies, achieved the fastest revenue growth among eight drug development inputs and services stocks tracked. The company's full-year revenue guidance surpassed analyst expectations. The sector overall performed strongly, with revenues beating consensus estimates by 4.1% and share prices rising 10.5% on average since earnings. Medpace's stock rose 10.2% following the results and currently trades at $582.23. The drug development inputs and services industry benefits from stable demand as pharmaceutical companies outsource non-core functions through medium to long-term contracts.

Yahoo Finance
Jul 22nd, 2026
Medpace beats Q2 revenue expectations by 2.6%, stock surges 18.6%

Medpace reported second-quarter revenue of $707.3 million, exceeding analyst estimates of $689.7 million and marking 17.2% year-on-year growth. The clinical research company's GAAP profit of $4.25 per share beat consensus estimates by 6.6%. The company raised its full-year revenue guidance to $2.85 billion at the midpoint, up from $2.81 billion previously. Full-year EPS guidance of $17.60 at the midpoint came in 3.9% above analyst expectations. Medpace's stock jumped 18.6% following the results. The company's adjusted EBITDA of $153.4 million also exceeded estimates, delivering a 21.7% margin. Despite the strong performance, analysts expect revenue to remain flat over the next 12 months, suggesting potential demand challenges ahead.

Yahoo Finance
Jul 21st, 2026
Medpace Q2 earnings preview: revenue expected to grow 14.3% year on year

Clinical research company Medpace Holdings will report its second-quarter earnings on Wednesday after market hours. The market expects Medpace's revenue to grow 14.3% year on year this quarter, in line with the 14.2% increase it recorded in the same quarter last year. In the previous quarter, Medpace reported revenues of $706.6 million, up 26.5% year on year, beating analysts' expectations. The company also exceeded EPS estimates, though its full-year EPS guidance aligned with analysts' forecasts. Analysts covering the company have generally reconfirmed their estimates over the last 30 days. Medpace shares have risen 15.8% over the past month, outperforming the life sciences tools and services segment average of 9.9%.