Clinical Research Associate (CRA/Senior CRA for In-House Opportunity). ...
We are prioritizing candidates with two plus years of cell therapy and or gene therapy, ophthalmology and rare disease or oncology experience as a CRA. ...
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...
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...
Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) preferred. CRC is responsible for the management and coordination of clinical research studies under the direction of the principal investigator (PI) and clinical research manager. Train and mentor junio...
Analytical - Synthesizes complex or diverse information; Collects and researches data; Designs work flows and procedures. ...
BIGO LIVE is seeking a talented, curious Business Intelligence Analyst who thrives at the intersection of data, product, engineering, and operations. Create and manage data pipelines in Excel, SQL or Python to aggregate data for different operations team. The team is data-driven and results focused....
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. ...
Join our team and bring your comprehensive clinical trial expertise to the forefront! We are seeking candidates with proven proficiency and hands-on experience across all phases of clinical trials (Phases 1-4), as clearly demonstrated on your resume. Experience managing clinical trials at the study ...
Train, supervise, and develop project team including Project Engineer, Project Superintendent, General Foreman and others. Work with upper management to optimize cash flow for the project, project billings and expenses for the duration of the project. Project Manager with experience in the commercia...
Senior Research Associate, Lead Discovery. We are looking for an experienced Research Associate to help the Discovery Sciences team accelerate our search for new oncology therapeutics. ...
We are seeking an experienced AI Trust and Safety Staff Research Scientist to spearhead our efforts in developing safe, ethical, and reliable AI systems. Experience leading research teams and mentoring junior researchers. Our AI stack is empowering consumers, startups, enterprises and scientists acr...
Our client needs a Clinical Research Coordinator to support one of their leading clinical sites with prospective clinical research studies. Clinical Research Coordinator (Onsite). Maintains research practices using Good Clinical Practice (GCP) guidelines. Strong knowledge and understanding of princi...
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...
A game changing I-O focused biotech with ambitions to change the landscape of antibody based autoimmune therapies, is hiring a Clinical Trial Manager to support their in house Ph. If you are interested in this Clinical Trial Manager role, feel free to send in your CV!. Coordinating and contributing ...
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...
In Vivo Research Associate - Contract - Redwood City, CA. Proclinical is seeking a dedicated and highly skilled In Vivo Research Associate. The In Vivo Research Associate will:. This role involves conducting in vivo research activities and executing preclinical studies to support the progression of ...
The employer is in the biosciences industry and the Research Associate will be joining a Research & Development group. An employer is looking for a Research Associate to join their team in San Diego, CA. ...
Senior Clinical Trial Manager / Clinical Trial Manager. Provide clinical trial support, mentoring, leadership, guidance, and direction to Clinical Research Associates (CRAs) assigned to clinical studies. This position offers a distinctive opportunity for a seasoned Clinical Operations Professional w...
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...
Develop and refine data collection systems and databases to ensure high-quality data for analysis and decision-making. The ability to manage data projects, visualize and communicate data findings creatively and effectively, provide analytical expertise, and create evidence-based recommendations for ...
Manager all project financials such as budget, costs, and deliver financial progress reports. About 5-10 years of experience working as a Project Engineer, must have a background working for an EPC or Engineering firm managing multiple projects and clients. They're looking for a Project Engineering ...
Hands on Project Manager (Operations/ Engineering/ Sales/ Tech). We are looking for an experienced Project Manager to join the organization, one of the fastest growing teams. You’ll get to partner with stakeholders horizontally and vertically within the organization - across product managers, engine...
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 ...
Develop and qualify flow cytometry-based assays for extended characterization to study immune cell biology and function, including creating SOPs and technical reports.Collaborate with QC teams to optimize methods, troubleshoot, investigate root causes, and manage method validation and lifecycle.Supp...