May be responsible for CRA and CTAs as direct reports. ...
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...
Markets and promotes low- to moderate-income home loans.Seeks opportunities through seminars, home buyer education forums, and home ownership classes to emerging market populations and low- to moderate-income individuals.Establishes and cultivates relationships with community organizations, and othe...
Through questioning the status quo and collaborating cross-functionally, the Manager, Clinical Operations provides leadership to a team of Clinical Research Associates (CRAs) and ensures the successful performance and delivery of his/her direct report’s project deliverables, on time with high qualit...
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...
Specifically, the staff research associate will participate in the operation of instruments available at the Core Facility and provide sequencing-associated services, including but not limited to DNA/RNA extraction and quantification, setting up of Sanger sequencer, next-generation sequencing platfo...
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned...
Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements. Provide guidance and training to clinical research staff. Assist with ma...
Reporting to our Associate Director of Clinical Operations, the. Prepares and maintains documents and files such as clinical study files, regulatory binders, and operations manuals for clinical sites (i. Has some understanding of the science behind Clinical Research, observes and gains exposure to c...
Avania is hiring Senior Clinical Research Associates (Sr CRAs) - West Coast - Extensive cardiology Class III device monitoring experience required. ...
Lead original research in foundation model and generative AI for automation. Collaborate with peers across research and product teams to foster innovation. Contribute to the broader application of your research within the company. Demonstrated excellence in research or significant product innovation...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
Supports and coordinates clinical trial activities and manages execution of 1 or more clinical trials/programs to ensure completion according to timelines. They are looking to bring on a Clinical Trial Manager to the team. Ideal candidate will have at least 5 years of relevant experience in either s...
Clinical Trial Manager / Senior Clinical Trial Manager. This role is a unique opportunity for an experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials in an industry setting and who has a strong knowledge of clinical operations, Good Clinical P...
The Clinical Trial Manager (CTM) is 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. This position will also work closely with a cross-functional team based in the ...
Senior Data Migration Quality Analyst – NO C2C, NO Sponsorship. Senior Data Migration Quality Analyst Overview:. We are seeking a highly skilled and experienced Senior Data Migration Quality Analyst to join our team. The ideal candidate will have extensive experience in data analysis, data quality a...
This role offers a unique opportunity for an experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials within an industry setting and a solid understanding of clinical operations, Good Clinical Practice (GCP), and FDA regulatory requirements. Hands...
A leading global financial services firm is seeking a talented Quantum Error Correction Research Scientist Computing Research to join a highly esteemed S&P 500 company. Quantum Computing Research Scientist. The successful candidate will collaborate with other researchers on both theoretical and expe...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
The Senior Research Assistant assists in entering and maintaining all documentation and records. Minimum two years of administrative/clerical experience required; one year research or laboratory experience preferred. Completion of LLU's educational program on "ethical use of human subjects in resear...
The Research Assistant supports the execution of certain aspects of a research project after the research design is established with minimal supervision. Able to read; write legibly; speak in English with professional quality; use computer, printer, and software programs necessary to the position; A...
Manage early-phase (1-2) oncology clinical trials. This preclinical-stage company leverages its proprietary platform to develop breakthrough therapies for solid tumors. Collaborate with CROs, vendors, and internal teams to ensure successful trial execution. Monitor trial progress and maintain regula...
Minimum of 4 years of experience in clinical trial management, with a strong track record of leading Phase I-III trials. Are you a seasoned clinical trial professional looking for a new challenge? Join this dynamic and innovative biopharmaceutical company, where they are dedicated to transforming li...
The Assistant Coordinator-Oncology Research serves as regulatory assistant and administrative support for the Oncology Clinical Research department in order to facilitate the implementation and management of oncology clinical trials, assists in document preparation and maintenance for study mandated...