The Clinical Trial Manager will lead activities associated with the evaluation, initiation and management of clinical studies to ensure compliance with SOPs, FDA regulations and ICH/GCP guidelines. Leads study management team, including oversight of CRO and Vendors. ...
Please note that relocation is offered for this position.
The Clinical Trial Manager is accountable for providing oversight to the site management activities outsourced to CROs for a number of phase II- IV clinical studies from planning and site feasibility ...
Our client is a global specialty pharmaceutical company that specializes in the development of new chemical entities and biopharmaceutical therapies. They have leveraged advances in antibody therapeutics to make tremendous strides in oncology, immunology and nephrology.
Job Posting Title:Consultant (Statistical Programmer)
Job Summary and Essential Functions:
A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies. ...
Our client, a reputable biotech company, is currently seeking a Manager, Regulatory Affairs . The Manager of Regulatory Affairs will report to the Director,Regulatory Affairs and is accountable for the preparation and management of simple andcomplex regulatory submissions ...
• Serves as the leader and coordinator for the execution and management of oncology clinical trial(s).
• Leads the study team’s identification and selection of CROs, KOLs and investigational sites.
• Manages the CROs in the initiation, management and ...
$130,000 - $200,000
Doctor of Philosophy
Biotech, Pharmacy, Science, Biology
Proactive individual to provide scientific oversight and management for strategic R&D partnerships and assist with projects in a fast-paced biotechnology company.
Sep 11 -
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