Clinical Study Manager Salary at Aadi Bioscience Inc BETA

About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Hourly Range: $20.00 - $22.50/hr (depe

Job Description Job Description Chief Operating Officer (COO) About Us SeraCollection Research Services is a leading Integrated Research Organization headquartered in Montebello, California. With over 21 years of experience in Clinical Research Management (Phases I-IV) and Clinical Sample Collection Trials for the diagnostic and biotechnology industries, we specialize in delivering safe, efficient, and high-quality clinical research solutions. We collaborate with a network of experienced Principal Investigators across Southern California to manage clinical trials effectively. Additionally, we operate Mobile Healthcare Clinics that support clinical trials and biological sample collection studies for Emergency Use Authorization (EUA) approvals on vaccines and testing devices. Our services have expanded to include point-of-care testing, vaccination programs for infectious diseases, and mental health services. Through our turnkey solutions—including mobilization, medical staffing, and supp

About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Hourly Range: $21.00 - $23.00/hr (depe

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit https://global.allerganaesthet

Job Description Job Description Long Beach Clinical Trials is seeking a CA Board Certified Physician to be a Principal Investigator (PI) to join our team on a per diem basis. The PI will be responsible for overseeing and managing clinical research studies, ensuring the integrity and accuracy of data, and providing guidance in all aspects of the research process. This position offers a flexible work schedule. Key responsibility: Conduct and oversee clinical trials, ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. Perform physical exams and review source data such as medical histories, medications, lab values to determine eligibility and safety of study participation. Access, review, and verify source data to ensure accuracy and alignment with protocol requirements. Provide leadership and oversight to other clinical staff. Participate in on-site and remote meetings and trainings with CROs and Sponsor.

About Us: Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Working Shift: (8am - 4:30pm) - Would

Job Description Job Description Job Title: Clinical Research Coordinator (CRC) Location: Los Angeles, CA, USA Job Type: Full-Time Salary: $25 - $35 per hour (based on experience and qualifications) About Us: Advancing Research International is an ophthalmology-specific Site Management Organization (SMO) conducting Phase I-IV FDA-regulated clinical trials. Headquartered in Los Angeles, CA, we operate satellite sites in Las Vegas, San Francisco, and Phoenix. Position Overview: We are seeking a highly organized and detail-oriented Clinical Research Coordinator (CRC) to join our team. The CRC will play a pivotal role in managing clinical research studies across our network, ensuring compliance with regulatory requirements, ethical guidelines, and study protocols. This is an in-house position, requiring direct collaboration with sites across our network. Bilingual English/Spanish is required. Key Responsibilities: Coordinate and oversee all aspects of clinical research studies, including pa

POSITION SUMMARY The Clinical Documentation Specialist monitors the quality of medical records and document by abstracting data, entering multiple stroke and research databases and ensuring quality improvement of data collection on stroke performance metrics and nursing metrics. This also includes assuring the medical records contain the mandated core measure data used to report to multiple regulatory agencies. The Clinical Documentation Specialist facilitates concurrent modifications to clinical documentation to ensure adequate information is included in the medical record about diagnosis, treatment, and follow-ups. They communicate and educate physicians, nurses, coding staff and other healthcare professionals to clarify issues and assure missing information is included to meet policies and regulations. They assist with clinical research recruitment, consenting, data collection, abstraction, and follow-up for clinical research trials. ESSENTIAL JOB FUNCTIONS AND CORE RESPONSIBILITIES