- Unknown (New York, NY)
- …activities of the compliance department. The ideal candidate will be adept at presenting CRA results to senior management and will be involved in the continuous ... responsible for providing subject matter expertise and leading the CRA team in conducting compliance risk assessments for various...plans to address any identified control gaps, managing the CRA process, and ensuring the team is up to… more
- ICON Clinical Research (PA)
- Senior CRA / CRA II - Home-Based,...of clinical development. We are currently seeking a Senior Clinical Research Associate or ... II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate . + In-depth knowledge of clinical trial… more
- Parexel (Austin, TX)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned ... Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and monitoring, managing...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
- ICON Clinical Research (PA)
- …shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate ( CRA ) to join our diverse and dynamic ... Senior Clinical Research Associate ICON plc is a world-leading healthcare...team. As a Senior CRA at ICON Plc, you will play a… more
- ThermoFisher Scientific (Middleton, WI)
- …skills, and abilities to perform the job (comparable to 2+ years as traveling clinical research associate ). Valid driver's license where applicable. In some ... 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical...by CTM (eg trip report review, newsletter creation, lead CRA team calls etc). + Facilitates effective communication between… more
- Parexel (Charleston, WV)
- The Senior Clinical Research Associate (Sr. CRA ) is responsible for the site management, site monitoring and close-out of assigned clinical ... Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable for site management and monitoring, managing...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years… more
- BeOne Medicines (Emeryville, CA)
- …follow-through with audit/inspection findings to resolution as it related to involved CRA staff. * Assist with other assigned clinical responsibilities within ... site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with… more
- ARTIDIS (Houston, TX)
- …are unique, the clinical studies are designed and supervised directly by ARTIDIS. The Senior Clinical Research Associate (SCRA) is an integral part ... the clinical studies. SCRAs work hand in hand with Clinical Quality Development, Clinical Research Associates (CRAs) and Clinical Study Managers… more
- IQVIA (Overland Park, KS)
- …IQVIA, we do not believe in a 'career ceiling.' You can make the Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated ... As you develop your career as a CRA , this role offers you the opportunity to...will also have a good basic knowledge of applicable clinical research regulatory requirements.You should have: +… more
- Abbott (Alameda, CA)
- …in life sciences preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate education and experience. + ... **The Opportunity** The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials… more
