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- 7-10 years of experience managing drug development projects and working with cross functional teams
- PMP or other Project Management accreditation is a plus
If interested, contact: Savio Rodrigues savio@sterlinglifesciences.com
Sterling-Hoffman Life Sciences
Home based support for liquid tumor studies/programs.
- in-house study management experience is required as is Oncology experience
- experience managing all the moving parts of a trial or multiple trials
As a Clinical Trial Manager (CTM), you have a wide range of responsibilities. We’re including a few of the big ones. Primarily, you will work to achieve the most successful clinical trial possible. You will lead cross-functional teams with Project Management, Clinical Operations, and Regulatory Affairs, while understanding and managing client expectations. You will proactively identify, resolve/mitigate, and escalate risks or issues when necessary.
- English fluency (ability to read, write, speak); fluency in host country language...
Requirements: 5+ years of experience in clinical research. TMF maintenance is very important. They are ideally seeking a candidate who has worked on the TMF through the submission process. This person will be managing 2 internal employees as well as managing the TMF vendor.
If interested, please contact Morgan McCormick (mmccormi@aerotek.com)
Regional Site Managers (CRAs) support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as SOPs and ensuring that study milestones are met. Central point of communication between investigational sites for all clinical trial related activities. Mentor to CRAs. Trial Lead CRA role when assigned. Performs additional roles and functions for US ICRO as assigned; such as participating/leading special project initiatives and committees. Is an essential...
Regional Site Managers (CRAs) support the goals of the organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as SOPs and ensuring that study milestones are met. Central point of communication between investigational sites for all clinical trial related activities. Mentor to CRAs. Trial Lead CRA role when assigned. Performs additional roles and functions for US ICRO as assigned; such as participating/leading special project initiatives and committees. Is an essential contributor...
Responsible for supporting the Senior Clinical Trial Manager/operational study lead, and for managing various aspects of the operational execution and delivery of quality studies, including in process quality control activities (e.g. quality checks and balances to ensure inspection readiness, Enrollment, Metrics, Milestones, Timelines and Budget).
Supports the Sr. CTM/operational study lead in collaborating with clinical affairs and other functions, and responsible for, the execution and delivery of studies (e.g. Clinical Planning,...
Below are the relevant details of the position for you to review, please pass along an updated resume and time your available to go over details to see if it's going to be a good fit with your background.
Responsible and accountable for several clinical trials.
Facilitate investigational site budget negotiations.
Manages each project within agreed upon timelines.
Provides regular updates to the staff, Sponsor, vendors and contract staff concerning status and progress of the trial.
Facilitate protocol and...
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Best Practices for your Clinical Trial
Are you aware of the latest regulations? One thing you can count on with our industry is that regulations are always updated and can be complex. Don’t worry! You can find all the information you need right here. (It’s stil up to you to read all of it though...)
