The Clinical Research Associate (CRA) II manages study activity from site selection, start-up, to close-out with adherence to regulations, maintaining data integrity, and aligning deliverables with corporate goals associated with the I-SPY Trials – www. ...
Clinical Research Associate (CRA/Senior CRA for In-House Opportunity). ...
Lead CRAI and CRA II team of 1-5, overseeing monitoring activities, supporting on-site and remote training, query resolution. The Clinical Research Associate (CRA) III manages study activity from site selection, start-up, to close-out with adherence to regulations, maintaining data integrity, and al...
We are looking for you! Our ideal candidate has deep experience and subject matter expertise with the Community Reinvestment Act (CRA) and is deeply committed to the mission of the CRA and its goals. We prefer a Commissioned Examiner via the Federal Reserve Examiner Commissioning Program (or another...
Responsibilities include but are not limited to:.Performing or coordinating aspects of clinical studies including site selection, study initiation, site monitoring, and study closeout.Maintaining communication with study investigators to ensure studies are completed in a timely fashion and ensuring ...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
We are looking for you! Our ideal candidate has deep experience and subject matter expertise with the Community Reinvestment Act (CRA) and is deeply committed to the mission of the CRA and its goals. We prefer a Commissioned Examiner via the Federal Reserve Examiner Commissioning Program (or another...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
As a Senior Clinical Trial Associate (Sr. Review study plans, including Clinical Monitoring, Communication, Project Management, and electronic Trial Master File (eTMF) Management. Clinical Trials Design and Management Certificate). Bachelor’s degree, preferably in biological sciences, health c...
Research Associate works under the direct guidance of the Project Manager- Research and the general guidance of the senior staff. Research Associate is proficient in animal procedures/animal husbandry, grant, internal, and/or contract research studies according to the study protocols and to the comp...
CTM will be responsible for the day-to-day oversight of global clinical trials and will manage internal stakeholders, CROs, multiple service providers, clinical monitors, and clinical trial sites. Structure Therapeutics is seeking a highly motivated Clinical Trial Manager (Sr. This position will als...
Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation. CRA will assist in the clinical execution and management of all...
Final date: Friday, Nov 21, 2025 at 11:59 pm (Pacific Time) Applications Research, Pathology, Physician, Scientist, Neuro, Experimental, Technology, Education. ...
Your colleagues will include internationally recognized experts in machine learning research as well as highly experienced technology and finance professionals. As an Administrative Assistant, you will directly support up to two senior managers and two mid-level managers. Participate in any on-site ...
We cross the entire spectrum of business, government, healthcare, education and entertainment and we’re currently seeking an experienced Project Manager to join our team. Ensuring the delivery of the project installation to the customer within the time and budget parameters of the project. Carrying ...
Ensure audit-ready condition of clinical trial documentation including central clinical files; review monitoring visit reports to ensure quality and resolution of site-related issues; coordinates and assist in the planning of regulatory or ethics committee activities, as appropriate. Oversee the per...
Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. Responsible for managing the research activities at sites participating in Worldwide’s clinical...
This role offers an exciting opportunity to contribute to ground-breaking research in a dynamic and innovative environment. As a Researcher for our client's Genomics Lab, you will be responsible for managing crucial operations, including overseeing outsourcing relationships, coordinating sample logi...
Clinical Operations plays a key role in ensuring all ****** clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of ******’s products. Clin...
Coordinate with project stakeholders (contractors, engineers, equipment suppliers) to ensure timely and cost-effective project development and delivery. Project Opportunity Research and Origination:. Collaborate with senior management and team members to create investment committee papers necessary ...
Clinical Research Associate (Part-Time). Collaborate with Contract Research Organizations (CROs) and vendors to ensure efficient delivery of study materials and documentation to investigator sites. Minimum of 2+ years of clinical monitoring experience in oncology trials required. ...
Clinical Operations plays a key role in ensuring all clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of company products. Clinical Tri...
The Clinical Trial Manager will manage and lead the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor activities and deliverables. The Clinical Trial Manager will have independent oversight of outsourced Clinical Studies includin...
Clinical Trial Manager will manage and lead the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor activities and deliverables. Clinical Trial Manager will have independent oversight of outsourced Clinical Studies including but no...
The CTM will ensure the timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs) and all applicable regulations governing the conduct of clinical trials while meeting Company goals and objectives. Assist in auditing clinical trial ...