Cra Salary at Brain Sentinel Inc BETA

About the Role: A growing clinical research team is seeking an experienced Clinical Research Coordinator II to join their site operations in San Antonio. This position plays a key role in managing day-to-day activities for assigned clinical trials, ensuring compliance with protocols, regulatory requirements, and internal SOPs. This role will also involve working unblinded, overseeing investigational product (IP) administration, and supporting junior team members. You will work closely with monitors, sponsors, and site staff to ensure high-quality research conduct and timely execution of study visits. Strong communication and organizational skills are essential, along with a proactive, problem-solving mindset. Key Responsibilities: • Manage daily operations of clinical trials, including patient visits and regulatory documentation • Perform phlebotomy, vitals, EKGs, and oversee IP administration and accountability • Serve as the lead coordinator on multiple studies, providing guidance an

What the PRN Registered Nurse does at Worldwide The PRN Registered Nurse (PRN RN), under the guidance of the Associate Director, Clinical Conduct and the Medical Director, is responsible for protecting the health, safety, and welfare of research participants by observing strict adherence to local, state, and federal regulations, Worldwide Clinical Trials (WCT) policies and procedures, and the Nurse Practice Act. They will also assist in setting up and overseeing procedures on the floor, performing various study related procedures, and administrative duties as needed. The PRN RN works under the direct supervision and guidance of the Associate Director, Clinical Conduct. They will provide direction and indirect supervision for the Floor staff to include Paramedics, Phlebotomists and Research Technicians. What you will do Under the direction of the Medical Director’s standing orders, functions as WCT’s medical coverage (along with on-duty Paramedics) in case of an emergency for subjects/p

Job Summary: Clinical Research Associates perform data research, and document production activities at the direction of physicians. Activities may include researching medical billing codes, researching scientific literature, sourcing cost data, working with medical cost/vendor surveys and cost analyses, and extensive proofing. To be considered, candidates must be ready to work in a fast-paced environment and be adept at multitasking and managing multiple projects at the same time. Advanced Microsoft Office Suite skills, excellent proofreading skills, a good attitude, a strong work ethic, and a firm commitment to deadlines are prerequisite. This position requires seven to eight hours per day of prolonged sitting. Essential Job Functions Develop and maintain proficiency with the use of the Company’s proprietary Workflow and Information Management System Understanding medical procedures, and their differences Assigning appropriate medical codes to various types of medical services and pro

Clinical Research Coordinator Great opportunity to collaborate on edge cutting Oncology clinical trials 1 year contract-to-hire (opportunity to go on permanently based on performance) 40 hours per week, 8-5PM M-F 100% ON SITE Position Overview: We are seeking a dedicated and organized Clinical Trial Coordinator to support patient visits and data management in a clinical trial setting. This role involves a mix of patient interaction, medication coordination, and documentation management to ensure that all trial activities are carried out efficiently and accurately. The Clinical Trial Coordinator will work closely with both the clinical and data management teams to ensure compliance with study protocols and regulatory requirements. Key Responsibilities: Daily Preparation: Upon arrival, the schedule for the day will be provided. Prepare for patient visits by ensuring all necessary kits, supplies, and equipment are ready for use. Medication and Dispensing Coordination: Allocate required me

Description The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START's mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population - leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey

Principal Investigator Job Description The Medical Doctor (PI) promotes Good Clinical Practice in the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to federal and state regulations and guidance documents. Primary Responsibilities: The PI assumes full responsibility for a clinical trial, including the oversight and ethical conduct of the study, maintaining integrity of the study design, and direction of the research team to ensure research is conducted in accordance with the local and national laws and regulations, including applicable FDA regulations, GCP, ICH guidelines, HIPAA, and all policies and procedures of the Sponsor, CRO and Site Evaluate patient eligibility for a clinical trial as per protocol Review and discuss study protocols and obtain (or delegate) informed consents

Job Summary: Location: San Antonio, TX (78229) Hours: Monday-Friday, 8am-5pm Pay: $28 - $31.25/hour The Clinical Research Coordinator (CRC) will work independently or under general supervision to manage and coordinate clinical research protocols. Reporting to the Director of Research and/or Principal Investigator (PI), the CRC will oversee the day-to-day operations of one or more concurrent clinical studies, ensuring compliance with research protocols, regulatory agency policies, and Good Clinical Practice (GCP) guidelines. This role will focus on clinical research in prostate and bladder oncology, including subject recruitment, data management, and coordination of all study-related activities. Key Responsibilities: Execute and manage all phases of clinical research protocols, ensuring adherence to specific study requirements. Coordinate data collection, specimen handling, and study operations across multiple departments and services. Maintain accurate and timely documentation, adherin

Job Title: Clinical Research Nurse (Research experience NOT required) Location: San Antonio, TX Contract Duration: 6-Month Assignment (NO opportunity to go on perm) Employment Type: Full-time, Contract Job Description: We are seeking a highly motivated and dedicated Clinical Research Nurse to join our team for a 6-month contract assignment in San Antonio, TX. The successful candidate will work with a multidisciplinary team to support clinical research studies, ensuring adherence to protocols, regulatory requirements, and participant safety. This is an excellent opportunity for someone looking to apply their clinical nursing expertise in a research setting. Key Responsibilities: Patient Interaction: Conduct patient assessments, including screening and enrollment, and provide education regarding the clinical trial process. Study Protocols: Ensure all research protocols are adhered to, including obtaining informed consent from study participants. Data Collection: Assist in the collection