Clinical Trial Manager

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.

Clinical Trial Manager at ICON, manages long-term strategic objectives including quality, timeliness, overall study performance and continuous process improvement in assigned clinical trials. CTM is responsible for all clinical trial activities within a country from study start up through final close out visit ensuring that organizational and regulatory requirements are met. 

What you will be doing:

• CTM will be the main local point of contact for CRAs and also the sponsor, and will guide the CRA team and will help them throughout the all phases.
• Manage multiple complex tasks requiring independent decision-making
• Interact with Operations team leader to determine team requirements
• Develop country budget and timeline
• Supervise site/investigator selection process
• Reviews and approves Monitoring Visit Reports submitted by SM; identifies issues and/or trends across a trial project and escalates deviation issues to the GTM and FM as needed
• Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial delivered within budget. Adheres to finance reporting deliverables and timelines.
• Ultimately responsible for the quality and timeliness of country trial performance in assigned
• Monitors country progress and initiates corrective and preventive actions when the trial deviates from plans and communicates study progress and issues to study management teams.

Experience required: 

• Life science degree 

• At least 3 years of experience as CRA or CTM in study monitoring, specially oncology experience is mandatory, Ideally, bladder cancer experience, however Solid tumor experience will be acceptable as well

• Strong working knowledge of ICH-GCP, company standard operation procedures, local

  laws and regulations, assigned protocols and associated protocol specific procedures.

• Strong IT skills in appropriate software and company systems.

• Willingness to travel with occasional overnight stay away from home according to

  business needs.

• Good written and oral communications skills as appropriate.

• Proficient in speaking and writing the country language and English language. 

• Good interpersonal and organizational skills.

• Ability to handle multiple priorities is essential

What is offered:

You will become part of one of leading company within the pharmaceutical industry. The client offers unique opportunity, professional working environment with focus on training and development opportunities. You will receive market conform remuneration package and other benefits.

Why 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.

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.

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, colour, 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.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.