Seeking Clinical Research Associate in Alameda, CA for 6-month project (potential extension). Manage Phase I-IV studies across USA, ensuring compliance with Federal Regulations and ICH guidelines. Develop study protocols and reports, monitor sites, a...
Seeking Clinical Research Associate (CRA) in Alameda, CA for 6-month project, potential extension. Conduct Phase I-IV studies, manage study operations, ensure protocol adherence, and oversee site activities. Requires 3-5 years' experience, knowledge ...
Research Nurse Coordinator II needed to oversee complex protocols involving investigational drugs/devices. Collaborate with stakeholders, train staff, ensure regulatory compliance, and assist in research protocol development. RN with 5-7 years of exp...
Join a top bioscience and IT company at NIH to work as a Sensory Research Technician advancing translational research in Bethesda, MD. Ideal for Neuroscience or Biology graduates with clinical research experience and expertise in neuroimaging, statis...
Seeking a Clinical Manager for remote role with 8+ years of pharma/biotech experience in CNS area. Manage trials, oversee projects, coordinate vendor selection, and ensure compliance with regulations. Strong PM skills, ability to forecast budgets and...
Seeking a Clinical Research Associate (CRA) in Alameda, CA for a 6-month contract. Requires 2+ years of clinical research monitoring experience. Responsibilities include writing study protocols, monitoring investigational sites, ensuring protocol com...
Seeking Clinical Research Associate with 2+ years experience in monitoring clinical trials. Responsibilities include planning and conducting studies, managing CRFs, and ensuring protocol adherence. Strong attention to detail and familiarity with ICH ...
Seeking a Medical Reviewer/Safety Reviewer in Columbus, OH for a 12-month project. Responsibilities include medical review of CRFs, managing CRAs, and providing support for Adverse Event Reporting. In-depth investigation and reporting of adverse even...
Join RemeGen Biosciences as a Clinical Trial Manager/Sr. Manager! Lead global clinical studies, manage vendors, contribute to protocol development, ensure data integrity, and adherence to timelines. Remote role open in Massachusetts, Pennsylvania, So...
Join a dynamic medical safety team as a key player, supporting adverse event collection and assessment for clinical products. Research, organize, and summarize vital medical information while assisting clinical study teams with safety matters. Ideal ...
