Senior Clinical Research Associate Salary at Altis Clinical Research Organisation BETA

JOB SUMMARY The Senior Clinical Research Associate will support clinical studies and the Clinical Operations Department by managing various administrative tasks, including generating agendas and minutes, maintaining study tracking, and conducting filing and quality reviews. This role, reporting to the Clinical Operations department's leadership, will also involve participating in process improvement initiatives across departments. The Sr. CRA will be instrumental in collaborating cross-functionally, working closely with study teams from vendors and CROs to achieve departmental and project goals. The Sr. CRA must adhere to the company's core values and comply with all applicable regulations, ICH-GCP guidelines, and SOPs. Strong candidates should understand trial and study site management, vendor management, and experience participating in the full cycle of studies from start-up to close-out. KEY RESPONSIBILITIES: Provide general administrative support to the Clinical Operations Departme

Job Description Job Description About Us Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of care in a healthcare facility. Our mission is to revolutionize patient care globally through transformational, accessible, clinically relevant diagnostic imaging. Learn More About The Role Job Title: Senior Clinical Research Associate Location: Palo Alto, CA As our Senior Clinical Research Associate (Senior CRA), you will play a crucial role in the planning, coordination, and execution of clinical studies, with a particular emphasis on post-market evidence generation. Your experience in neuroscience, MRI technology, and medical devices will be pivotal in ensuring the quality and compliance of our clinical trials. You will work closely with cross-functional teams to support c

About the Company: Humannity Medtec’s Clinical Affairs team is currently accepting applications for a Clinical Research Associate II/III for a full-time position (hybrid) based in Valencia, CA. This position plays an essential role in the development and implementation of clinical research projects by supporting the clinical activities of assigned studies. About the Role: Responsibilities include the planning, execution and interpretation of clinical research and data collection activities. This position plays a key role in the development and execution of pre-clinical, First in Human and pivotal trials intended to support regulatory registration of novel medical devices, as well as physician-initiated and company-sponsored clinical trials. Responsibilities: Ability to autonomously manage all clinical activities related to the execution of US/OUS Class 3 medical device clinical trials consistent with GCP and other regulatory and compliance requirements. Drive activities related to the

Position Summary The Sr. Clinical Research Associate is responsible for leading, assisting, and providing monitoring and site management support for clinical sites during study start-up, enrollment, maintenance, and close-out. Responsibilities Lead or support assigned clinical trial sites(s) during start-up, ongoing activities, close-out, and reporting. Assist with the review of study-related and essential clinical study start-up documents including but not limited to Clinical Protocols, Informed Consent Form, Monitoring Plans, Case Report Forms (CRFs), and Site Training Materials. Conduct or assist in site visits including Site Qualification, Site Initiation, Interim Monitoring, and Close-Out Visits. Train study site personnel to study conduct, protocol, and database. Ensure sites are entering data, responding to data queries, and closing out action items in a timely fashion. Prepare confirmation and close-out letters and study visit reports. Review site essential documents to maintai

Job Description Job Description · 3 - 6 years of experience with CRA tasks such as remote monitoring, SOP creation, site selection setup, setup execution, protocol development; medical device experience is preferred. Qualifications: · Preferred if they have at least one CRA job experience from the sponsor side · If they have only CRO-based experience, then being coachable is required · We have found that many CRO-focused candidates have a more narrowed experience with repetitive core CRA tasks directed by a manager (we understand this is a common CRO model with team resources assigned to discrete functional tasks). · Our model has more of an expectation that Sr/CRAs will be flexible and able to anticipate, pivot, independently lead tasks and lead others (so we screen for people who can: wear multiple hats (using knowledge of regulations, data management, document creation etc.) throughout all phases of the study, be able to troubleshoot during study execution and perform with little to

Job Description Job Description This Remote position located in the USA will be working with Provident Research Inc. in a dedicated Functional Source (embed) relationship. Our client is a major manufacturer of Medical Devices and this role is responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the Organization. Interviews are being scheduled now to fill immediate openings. Previous Medical Device experience Mandatory. Responsible for managing clinical study activities for multiple sites in single or several Clinical Projects. Oversees performance of appointed study sites conducting company initiated clinical studies. Responsible for the site visits, monitoring, communication and deliverables for the assigned study sites. Serves as a member of the clinical study team and is the liaison between Clinical Operations and Study Site personnel for the specific clinical projects. This opening is imme

Job Title: Senior Clinical Research Associate (CRA) Location: East Coast Job Type: Contract Start Date: January 2025 Length: 2 years Hours: 30-40 hours per week W2 ONLY! Job Summary: We are seeking a highly experienced and motivated Senior Clinical Research Associate (CRA) to join our dynamic team. The ideal candidate will have extensive experience in early phase (Phase 1 and 2) clinical trials, particularly in Oncology with a focus on Solid Tumors. This role involves overseeing clinical trial sites, ensuring compliance with protocols, and maintaining high standards of data integrity. Key Responsibilities: Site Management: Oversee and manage clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Monitoring: Conduct regular site visits to monitor study progress, verify data accuracy, and ensure the safety and well-being of study participants. Data Entry and Management: Ensure accurate and timely entry of clin

Job Summary: CTM Associate II plays a key role in managing and coordinating clinical trials that focus on biomarker and bioanalytical research. This position is responsible for ensuring the efficient execution of clinical studies from initiation through to completion, with a focus on biomarker discovery, validation, and bioanalytical testing. Key Responsibilities: Assist in the planning, coordination, and execution of clinical trials involving biomarker and bioanalytical research. Ensure compliance with study protocols, regulatory guidelines, and ethical standards throughout the trial lifecycle. Collaborate with laboratory teams to manage biomarker collection, storage, and analysis as part of clinical trial protocols. Ensure that bioanalytical data is accurately captured and recorded in the study database. Assist with regulatory submissions and maintain documentation related to biomarker and bioanalytical trials. Monitor and ensure compliance with Good Clinical Practice (GCP), FDA regu