Clinical Trial Manager

ICON Strategic Solutions; Brasil; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

An established industry player in healthcare research is seeking a Clinical Trial Manager to lead cross-functional teams in delivering successful clinical trials. This role involves overseeing project deliverables, managing client relationships, and ensuring high-quality standards throughout the trial process. With a strong emphasis on professional development and a commitment to employee wellbeing, the company offers a competitive rewards package and a supportive work environment. If you have a passion for clinical research and a drive to make a difference, this opportunity is perfect for you.

Qualificações

• Solid clinical research experience and strong background in clinical trial management.
• Fluency in English required for effective communication.

Responsabilidades

• Lead cross-functional teams to ensure successful clinical trials.
• Manage client expectations and proactively identify risks.

Conhecimentos

Clinical Trial Management

Project Management

Risk Management

Customer Relations

Oncology Cellular Therapy Trials

Formação académica

Undergraduate degree in clinical, science, or health-related field

Licensed health-care professional (e.g., registered nurse)

Descrição da oferta de emprego

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

What will you be doing?

As a Clinical Trial Manager, you have a wide range of responsibilities. We’re including a few of the big ones. Primarily, you will work to achieve the most successful clinical trial possible. You will lead cross-functional teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitigate, and escalate risks or issues when necessary.

• Provide Project Oversight and Leadership for Clinical Deliverables
• Project Resourcing
• Quality - Training & Development
• Project Finance
• Customer Relations (Internal & External)

What You Need to Have:

• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse); or equivalent work experience, required
• Solid clinical research experience, required
  • Solid experience in clinical trial management, strongly preferred
  • Solid monitoring experience, strongly preferred
  • Experience in managing complex or global trials, preferred
  • Solid experience leading Oncology cellular therapy trials, strongly preferred
  • Experience in managing all trial components (start-up to database lock), preferred
• English fluency (ability to read, write, speak), required

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.