Manager, Clinical Operations

Pharmaceutical Research Associates, Inc; Brasil; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

An established industry player in healthcare intelligence is seeking a Manager for Clinical Operations. This role involves overseeing CRAs and CTAs, ensuring high performance and quality in clinical studies. The ideal candidate will demonstrate leadership, strategic agility, and therapeutic expertise, contributing to a culture of continuous improvement. Join a forward-thinking organization that prioritizes employee development and offers a comprehensive rewards package, ensuring your career growth and well-being. If you're passionate about making a difference in clinical research, this opportunity is perfect for you.

Qualificações

• Experience as Senior CRA leading and mentoring junior monitors.
• Ability to acquire and maintain therapeutic expertise.

Responsabilidades

• Line manage CRAs and/or CTAs ensuring high performance.
• Assist in oversight of site management activities for clinical studies.
• Create a culture of process improvement and streamline processes.

Conhecimentos

Leadership

Strategic Agility

Therapeutic Expertise

Communication Skills

Formação académica

Bachelor’s degree in a scientific or health-related field

Descrição da oferta de emprego

Overview

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.

Responsibilities

Main activities:

1. The role of the Manager, Clinical Operations is to line manage CRAs and/or CTAs effectively, ensuring high performance, quality and continuous development, including interviewing, evaluating and selecting CTAs and CRAs.
2. Assist Amgen in performing oversight in fulfilling its site management activities and obligations in relation to clinical studies as the primary sponsor of those studies.
3. Create a culture of process improvement with a focus on streamlining processes adding value to our business and meeting Amgen needs.
4. Onsite assessment visit with each CRA once a year.
5. Work according to and comply with relevant ICON/DOCS procedures and processes.

Qualifications

• Bachelor’s degree or equivalent in a scientific or health-related field.
• Experience as Senior CRA leading and mentoring junior monitors, as Coordinator CRA or related roles preferable.
• Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needs.
• Demonstrated strategic agility & broad business acumen.
• Demonstrated leadership behaviors with ability to accept challenges, seek opportunities to remove barriers, influence without authority, and lead in areas of uncertainty.
• Read, write, and speak fluent English; fluent in host country language.

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.