skip to main content

Important Notice

It appears you are using an older version of your browser. While some functions will be available, Delaware JobLink works best with a modern browser such as the ones provided by:

Please download and install the latest version of the browser of your choice. We apologize for any inconvenience.



Clinical Trial Manager - Oncology/Biotech (Home-based)

Click the Facebook, Google+ or LinkedIn icons to share this job with your friends or contacts. Click the Twitter icon to tweet this job to your followers. Click the link button to view the URL of the job, which then can be copied and pasted into an e-mail or other document.

Job Details
Job Order Number
JC146468611
Company Name
ICON Clinical Research
Physical Address

Newark, DE 19713
Job Description

Clinical Trial Manager – Oncology/Biotech
Home Based anywhere in US

As a CTM you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
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
Role Requirements

Must have experience in Oncology experience
Must have previous experience in a Clinical Trial Manager role.
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

ICON Plc is an equal opportunity employer. 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.

For more information about personal rights under Equal Employment Opportunity, visit:
EEO is the Law

EEOC Poster


To view full details and how to apply, please login or create a Job Seeker account.