Clinical Research Associate Salary at Ecog-Acrin Cancer Research Group BETA

Clinical Trial Associate – Leading Biotech in Cardiac & Gene Therapy A pioneering biotech company specializing in cardiac gene therapy is looking for a Clinical Trial Associate to join their team. This position offers the opportunity to work with breakthrough therapies focused on transforming cardiac care for patients with severe heart conditions. As part of this role, you’ll collaborate with leading experts and play an active role in the execution of high-impact clinical trials. Role Responsibilities A Clinical Trial Associate (CTA) plays a crucial role in the administration and coordination of clinical trials, which are research studies designed to evaluate the safety and efficacy of medical interventions such as drugs, devices, or treatment protocols. Below are the primary responsibilities and skills associated with the role: Key Responsibilities: Document Management: Maintain and organize essential trial documentation (e.g., study protocols, case report forms, informed consent form

ICON Dedicated to a Single Sponsor Rare Disease Studies 2 to 4 protocols 8 to 10 sites Sites – Regionally Aligned unless assisting in co-monitoring which may be a region over. Opening looking for a CRA to cover the North East. 8 visits per month Mix of remote and on-site. Mostly 1 day visits Smaller program. Family oriented. Cohesive team. Great relationships between management and CRAs. Requirements: Does not require a four-year degree, completed all visits independently and have two plus years of monitoring experience. Sponsor looks for a candidate to start within 30 days of accepting the position. CRA II Only - Does not have a CRA III/Sr. opening at this time. MUST BE LOCATED IN THE NORTH EAST What you will be doing: Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providin

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

Clinical Research Associate I/II Location: East Coast, USA (Remote-based with Travel) About Us We are a dynamic and innovative biopharmaceutical company dedicated to advancing cutting-edge therapies in the cardiovascular field. We are seeking a motivated and detail-oriented Clinical Research Associate (CRA) I/II to join our expanding team. This role offers an exciting opportunity to contribute to meaningful clinical research while collaborating with a passionate and supportive team. Position Overview As a Clinical Research Associate I/II, you will play a vital role in ensuring the successful conduct of clinical trials across our East Coast research sites. This position requires an individual who is organized, proactive, and comfortable with frequent travel. You will be responsible for monitoring study sites to ensure compliance with protocols, regulatory requirements, and company standards. Key Responsibilities Conduct monitoring visits at clinical trial sites (average of 8 visits/mont

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

Vaccine Clinical Research Associate 3 to 5 protocols 5 to 8 sites If any sites are high enrolling that the monitor’s site load will be reduced. 8 to 10 days on-site per month Therapeutic areas: Vaccines trials. Vaccine trials are fast-paced with quick database cleaning demands. Healthy subject populations do not have very many SAEs Very few regulatory documents related to study changes compared to other therapeutic areas Requirements: Must have a four-year degree, completed all visits independently and have one year of independent monitoring. Open to any therapeutic experience. What will you be doing? As a Clinical Research Associate, you will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. Applies knowledge of ICONs policies and procedures Demonstrates excellent written

We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes and site management. Key Responsibilities: Lead and manage start-up activities for clinical studies, ensuring compliance with local and international guidelines (ICH-GCP). Prepare, review, and track site regulatory documentation. Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones. Participate in Local Study Team meetings and report on site performance metrics. Ensure timely submission of documents to regulatory authorities and maintain the trial master file (eTMF). Qualifications: Minimum 3 years of experience in Clinical Study Start-Up (full-time). At least 1 year of hands-on experience with Veeva Vault. Strong background in informed consent review and negotiation. Bachelor’s degree (higher degree preferred) with knowledge of clinical trial processes (Phase

Job Details Job Location Main Corporate Office - Malvern, PA Description Job Purpose The Clinical Research Associate is a key member of Ocugen's clinical trial management team and integral to the successful planning and execution of clinical studies. This individual will develop and maintain strong, productive relationships with both the clinical sites and CRO and is responsible for the oversight of clinical monitoring activities. Duties and Responsibilities: Support study management team to ensure that studies are conducted in adherence to study protocols, applicable SOPs, ICH/GCP guidelines and government regulations Assist study team(s) in the identification, feasibility assessment, qualification, and selection of clinical research sites Drives the study start-up process in conjunction with the CRO ensuring timely submission of regulatory documents and completion of clinical trial agreements and budgets Interface with clinical sites to ensure timely and accurate completion of study