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Company | Jobot |
Address | Brooklyn, NY, United States |
Employment type | FULL_TIME |
Salary | |
Category | Nanotechnology Research,Research Services,Biotechnology Research |
Expires | 2023-06-12 |
Posted at | 1 year ago |
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Why join us?
Why join us?
- Maintain accurate and up-to-date study documentation, including monitoring reports, site visit reports, and study-related correspondence.
- Ensure the safety and welfare of study participants by monitoring adverse events and serious adverse events.
- Identify and escalate study issues to the appropriate stakeholders, including the clinical project manager, medical monitor, and regulatory affairs.
- Conduct clinical monitoring activities at investigational sites to ensure compliance with study protocols, regulatory guidelines, and SOPs.
- Ensure timely and accurate data collection and entry into the electronic data capture system.
- Collaborate with cross-functional teams to ensure the successful execution of clinical trials, including data management, biostatistics, and medical writing.
- Perform site qualification, initiation, and close-out visits, including site selection, site initiation, and site closure.
- Strong organizational and time-management skills.
- Experience in oncology and solid tumors is required.
- Bachelor's degree in life sciences or related field.
- Ability to travel up to 50% of the time.
- Knowledge of clinical trial design, conduct, and analysis.
- Familiarity with regulatory guidelines and SOPs.
- Excellent communication and interpersonal skills.
- Ability to work independently and collaboratively in a team environment.
- Minimum of 2 years of experience as a CRA in the biotechnology or pharmaceutical industry or academic space
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