Clinical Trial Manager

This is an exciting opportunity to join ICON

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is a serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

The Clinical Trial Manager is expected to act as the Functional Lead from Clinical Research Services with responsibility for delivery of all clinical aspects of clinical studies. To oversee and serve as the liaison between the Project Manager and a group of Clinical Research Associates (CRAs) assigned to a given clinical study, for the delivery of all aspects of monitoring and site management, ensuring consistency with ICH/GCP and applicable ICON Standard Operating Procedures (SOPs), applicable regulations, the Monitoring Plan and ensuring the clinical portion of the study is inspection ready at all times.

Responsibilities

• The primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients

• Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects

• Contribute to the development and maintenance of cross-functional project management plans

• Responsible for risk mitigation strategies, associated action plan, and issue resolution

• Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff

• Provide direction and support to the Clinical Operations study team

• Collaborate with Business Development (BD) to ensure timely completion of change orders

• Track Clinical Operations project deliverables using appropriate tools

What You Need

• Must have at least 3 years Clinical monitoring experience
• University/Bachelor's Degree in medicine, science or equivalent degree/experience.

• A satisfactory progression of monitoring experience with previous experience in leadership and/or management activities

• Previous working experience within the clinical trial management field.

• Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.

• Some knowledge of project management processes and tools.

• Fluent in written and spoken English.

• Computer literate.

• Due to the nature of this position, it may be required for the employee to travel approx 25%. Therefore, dependent on the employee's location, the employee may be required to possess a valid Driver's license.

Why join us?

Ongoing development is vital to us, you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skillset. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.

ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.

EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origi