Jobs

NewYorkBIO members have the benefit of posting jobs to our Job Board below. 

You can also visit the career pages of some of our members by clicking on their names.

Merck, Vertex Pharmaceuticals, Pfizer, PHCBI

 

6 hours ago | Management | New York
LOCATION: New York, NY

STATUS: Regular, Full-Time

REPORTS TO: Executive Director/Head of Clinical Operations & Project Management

SUMMARY: The Senior Clinical Trial Manager will be responsible for working with all departmental functions to develop and implement study processes and procedures to ensure the timely execution of quality clinical trial. The Senior/Clinical Trial Manager will act as a key contact for external stakeholders like CROs and vendors and internal stakeholders like SVP of Clinical Development to address study issues and support the successful execution of clinical trials.
6 hours ago | Management | New York
LOCATION: New York, NY

REPORTS TO: CEO

SUMMARY: Oncology-experienced regulatory affairs specialist who will provide, develop and lead regulatory strategies to maximize global regulatory success towards achievement of clinical development programs involving investigational or marketed products and provide strategic and tactical advice to teams to achieve timely and efficient development of programs, while ensuring compliance with applicable regulatory requirements.
6 hours ago | Management | New York
LOCATION: New York, NY

STATUS: Regular, Full-Time

REPORTS TO: Senior Clinical Trial Manager

SUMMARY: The In-house Senior CRA will be responsible for assisting the Clinical Trial Manager to develop and implement study processes and procedures in the execution of clinical trials.
6 hours ago | Management | New York
LOCATION: New York, NY

STATUS: Regular, Full-Time

REPORTS TO: Senior Vice President, Clinical Development

SUMMARY: Involvement in all aspects of clinical trial design and execution, including authoring protocols, medical content and leadership of the clinical studies, with particular focus on EU, site initiation, medical monitoring (including review adverse events) and data interpretation and reporting. This position must have experience with pediatric clinical trials, specifically in oncology.
2 months ago | New York
Involvement in all aspects of clinical trial design and execution, including authoring protocols, medical content and leadership of the clinical studies, with particular focus on EU, site initiation, medical monitoring (incl. review adverse events) and data interpretation and reporting.
3 months ago | New York
SELLAS Life Sciences is a global biotechnology company focused on the development of novel therapeutics designed to treat diseases in oncology. In this newly created position, the TMF Manager will oversee and manage the set-up, maintenance and archival of the Trial Master File (TMF), including the tracking, reporting and analysis of metrics related to clinical trial documentation and administration of the electronic TMF (eTMF). The TMF Manager will be responsible for, among other things, ensuring an audit-ready TMF to achieve and maintain inspection readiness at all times, while driving completion of the TMF.

Savings Partners