|
To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

| Job #02382 |
 |
| About our client |
| Our client is a company focused on proprietary therapies for the treatment of cancer. The company is also keenly occupied in evaluating new therapeutic agents and related technologies for in licensing. |
| Position |
Location |
| Senior CRA/Clinical Trial Manager |
New Jersey |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Co-monitor with CROs when necessary 2) Work with EDC vendor on writing edit checks/queries 3) Report to Senior Director, Clinical Operations on progress of studies 4) Assist in planning investigators’ meeting 5) Present information at the meeting to familiarize investigators with the protocol and monitoring procedures 6) Attend investigator and kick-off meetings, monitoring training and various CRO (or other vendor) meetings 7) Perform administrative tasks as needed to support project 8) Work with EDC vendor to create screens and write edit checks |
| Requirements |
1) Bachelor’s degree 2) Experience in monitoring oncology clinical trials 3) Minimum 5 years of clinical research experience in a pharmaceutical company 4) Good understanding of data management – query process 5) Ability to manage and communicate effectively in a team 6) Strong attention to details in composing and proofing materials, establishing priorities, scheduling and meeting deadlines 7) Ability to work in a fast-paced environment 8) Demonstrated ability to juggle multiple competing tasks and demands 9) Ability to independently present complex information to Senior Director Clinical Operations and CROs 10) Ability to prioritize multiple projects 11) Ability to work successfully within a cross-functional team 12) Ability to work independently, take initiative and complete tasks to deadlines 13) Strong knowledge of MS Word, Excel, PowerPoint and Outlook 14) Willingness to travel (flexible) |

|
|
|