about 1 year ago
Salary: Dependant on experience
About my Client: I am looking for a Clinical Trial Associate for an exciting small Medical Device company working in oncology. They are using cutting edge technology to eliminate cancer. My client is using a ground breaking product that the FDA has recently granted them for the illuminating of breast cancer which has gone through phase III and have five others waiting for approval.
They are looking for a self-motivated candidate, focused on progressing their career quickly, have greater involvement in key decisions, increased recognition and the ability to make a difference in this exciting opportunity.
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Maintain and quality audit to assure the most recent revisions of documents are on project portals
Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
Maintain version and quality control of project documentation and submit to trial master file
Assist with the tracking and maintenance of project related information, including site medical question and answer log
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Maintain current participating site and personnel information
Arrange and track the distribution of project specific training to the project team
Excellent oral and written communication and planning skills
Meticulous attention to detail
Ability to manage tasks
Degree educated desirable (life sciences preferred) or equivalent combination of education, training and related experience.
If you are interested in hearing more about the role, message me on LinkedIn or e-mail me with your CV on