div class="c-virtual_list__item" id="message-list_1763049962.052619">The expected salary range for this role is $60,000 - $90,000 USD per year for full time team members.
With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress.
By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
Performs routine operational activities for multiple research protocols · Liaise between site research personnel, industry sponsors, and Supervisor · Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable · Coordinates schedule of assessments from initial submission of feasibility until study closeout · Reviews the study design and inclusion/exclusion criteria with physician and patient · Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements · Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data · Creates study specific tools for source documentation when not provided by sponsor · Collects, completes, and enters data into study specific case report forms or electronic data capture systems · Generates and tracks drug shipments, device shipments, and supplies as needed · Ensures timely and accurate data completion · Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations · Communicates all protocol-related issues to appropriate study personnel or manager · Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required · Reviews and responds to any monitoring and auditing findings Education/Experience: · Bachelor's Degree or 1+ year of equivalent experience required Certifications: · Certified Clinical Research Coordinator preferred Benefits TriStar Centennial Medical Center, offers a total rewards package that supports the health, life, career and retirement of our colleagues. Job Summary and Qualifications The Clinical Research Coordinator position is responsible for coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors.
Nashville, TN30+ days ago
p>Perform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
li>Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.
By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals.
Nashville, TN30+ days ago
p>Aligning with Vanderbilt Health's Strategic Directions, the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year.
By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies.
We are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies.
Germantown, TN18 days ago
Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Mt. Juliet, Tennessee30+ days ago
div>Tennessee Oncology, one of the nation’s largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country.
This position works closely with the research team to learn and assist with a variety of clinical research activities.
p>We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need.
Johnson City, TN30+ days ago
p>The Clinical Research Coordinator will interface basic researchers and clinicians by facilitating specimen accrual to translational studies, particularly a new initiative with UTHSC focusing on genomic data merged with clinical data. Aligned with the institution''s mission, we value efforts to engage in teaching, scholarship, creative activities, and service that involve community partners and address significant societal needs in our region and beyond.