Clinical Research Data Associate - Schizophrenia Studies (Per Diem)
NYU Langone Health
NYU Langone Health is seeking a Research Data Associate (RDA) to support clinical research in the Schizophrenia Research Group. The RDA will assist with participant recruitment, study procedures, and data analysis under the supervision of the Principal Investigator. This role requires an Associate's degree and experience in a research setting is preferred. NYU Grossman School of Medicine offers a thorough benefits package, including financial security and a wellness program. #J-18808-Ljbffr
- A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have...Suggested
$25.84 - $34.06 per hour
NYU Langone Health is seeking a Research Associate (Per Diem) to support clinical and translational studies within the Center for Surgical and Transplant Applied Research... ...Responsibilities include participant recruitment, data collection, and maintaining study documentation...Daily paidHourly payFlexible hoursDay shiftAfternoon shiftEarly shift$29.55 per hour
...opportunity to join our team as a Research Data Associate. The Research Data Associate (RDA) will work per diem to contribute to clinical research efforts within the Schizophrenia Research Group at the... ...RDA will provide support for studies focusing on the development of...Daily paidHourly pay- ...in New York City is hiring a Clinical Research Assistant I to support daily... ...of clinical research studies. Responsibilities include collecting... ...and recording study data, assisting in grant applications... .... Candidates should have an Associate's Degree in Science or related...SuggestedHourly pay
- ...educational institution is searching for a Research Assistant within the Department of Neurology. This role involves overseeing clinical research studies, ensuring regulatory compliance, and... ...structured work schedule of 35 hours per week in New York, with a competitive...SuggestedWork at office
- ...York City is looking for a Clinical Research Assistant I to support various... ...collecting and organizing data, assisting in grant preparation... .... Candidates should have an Associate Degree in Science or... ...contribute to important medical studies while gaining valuable experience...
- A leading healthcare institution is seeking a Research Associate in New York City. This position involves conducting independent basic science experiments and collecting clinical data, with a focus on training new staff in research methodologies. Candidates must have a...Daily paidFlexible hoursAfternoon shiftEarly shift
$29.55 per hour
...Research Data Associate, Temporary Per Diem Full Time Research Support Staff New York, NY • ID: 1157461_RR00116714 • Temporary... ...for providing direct data and/or clinical research in support of clinical trials, studies and general research under direct supervision...Daily paidHourly payFull timeTemporary work$29.55 - $35 per hour
Position Summary Research Data Associate - Per Diem. Provide direct data and/or clinical research support for clinical trials, studies and general research under direct supervision. Work with School of Medicine and Medical Center staff and departments, including Directors...Daily paidHourly pay$75k - $80k
...We are looking for a seasoned Clinical Research Coordinator who is interested... ...various sites to work as a Study Coordinator. Weekend travel is... ...covered along with a daily meal per diem and candidates must live... ...conducted accurately Collects data as required by the protocol and...Daily paidContract workRemote workWeekend work$125k - $145k
...requirements, i.e. Good Clinical Practice (GCP) and... .... Provide protocol and study related training to assigned... ...issues appropriately per the escalation pathway.... ...as necessary. Supports research sites with local Institutional... ...with site staff and data management to resolve...Contract workLocal areaRemote workFlexible hours$90k - $140k
...who take healthcare and clinical research personally, with... ...hiring a Clinical Research Associate II or Senior Clinical... ...responsible for ensuring the data remains audit ready... ...8-10 site visits days per month (up to 80%... ...activities, inclusive of all study visit types (PSV, SIV,...Hourly payCurrently hiringLocal areaRemote work- ...device company focused on cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study sites. The ideal candidate will have 3-5 years of clinical monitoring...Remote work
$71.9k - $189k
...sites are conducting the study(ies) and reporting study data as required by the study protocol... ...scope of work and Good Clinical Practice. • Work with... ...subject recruitment plan on a per site basis. • If... ...applying, applicable clinical research regulatory requirements....Full timePart timeLocal areaImmediate startWorldwide- ...Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the... ...protocol/process deviations Perform source data verification and follows up on data...Work visa
- ...Clinical Research Associate Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or... ...designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate and...
- ...Baylor College of Medicine is seeking Clinical Research Associate for a role focused on projects integrating... ...investigators to support day-to-day study activities and progress of clinical... ...and/or conduct , and analyze interview data related to AI-based “defacing” technologies...Remote work
$115k - $125k
...Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research... ...and manage communication with study sites. Assess site adherence to protocol... ...including regulatory approvals, enrollment, data collection, and query resolution....Permanent employmentWork at officeRemote work- ...Clinical Research Associate (CRA) – Cardiovascular Medical Device MiRus is an innovative healthcare company... ...management of cardiovascular clinical studies for MiRus products with a focus on... ...caliber document development and quality data collection. The applicant should...Remote workRelocation packageMonday to FridayFlexible hours
- ...Summary In this Clinical Research Associate role (may be contract or full‑time employee... ...the progress of clinical studies, either at investigative sites... ...expected: ~1+ site visit per week, for sites that do not... ...medical records (EMR)/patient data Source documentation verification...Full timeContract workInterim roleLocal areaRemote work
- ...A leading healthcare organization is seeking a Clinical Research Associate in Connecticut to monitor oncology studies and ensure compliance at investigational sites. The ideal candidate will have a Bachelor's degree in Life Sciences or be a qualified RN, with 2+ years...
$91.34k - $114.17k
...healthcare intelligence and clinical research organization. We're proud to... ...seeking a Clinical Research Associate to join our diverse and dynamic... ...complex medical data, and contributing to the advancement... ...staff to facilitate smooth study conduct. Performing data...Work experience placementFlexible hours$71.9k - $169.3k
...Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key... ...clinical sites to ensure compliance with study protocols, regulatory requirements,... ...integrity and quality of clinical research data. Key Responsibilities Conduct...Full timePart timeImmediate startWorldwide- ...Our Client is a rapidly growing international Clinical Research Organisation offering an experienced( Senior ) CRA opportunity to work from... ...Conducting start-up activities and monitoring visits Maintaining study files, writing clinical trial reports and liaising with...Work from home
$120k - $140k
.... Salary: $120,000 - $140,000 per year A bit about us: Prep-Ipo... ...including but not limited to Pre-study visits, initiation visits,... ...using various tools to ensure data generated at the site are complete... ...management Work with in-house Clinical Trial Assistant to collect,...Interim roleLocal areaRemote workFlexible hours$108.7k - $139.8k
...All Jobs Senior Clinical Research Associate The Senior Clinical Research Associate... ...for monitoring excellence, data integrity, and site engagement... ...full lifecycle of a clinical study. The Senior CRA brings... ...main office (up to one week per month) and attendance at industry...Contract workWork at officeRemote workNight shift- ...Senior Clinical Research Associate (US) Remote Position Summary The Sr. CRA is responsible for the oversight... ...are conducted in compliance with the study protocol, ICH-GCP guidelines,... ...oversight or monitoring of site performance, data quality, patient safety, and timely...Interim roleRemote work
- ...Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device... ...well-executed plan for communication with the study teams and sites. Well-versed in clinical trial...Full time
$91.5k - $137.3k
...involving start-up and study implementation, on-site monitoring of clinical research studies as well as on-going... ...protected, quality of data generated by managed... ...required project documents as per SOPs, Clinical... ...Verifies issues or risks associated with blinded or randomized...Contract workLocal areaRemote workNight shift$102k - $162k
...Job TitleSenior Clinical Research AssociateJob DescriptionThe... ...Senior Clinical Research Associate is responsible for developing comprehensive study plans/protocols,... ...objectives to ensure robust data integrity and study... ...person at least 3 days per week. Onsite roles require...Full timeWork at officeImmediate startRemote workWork visa3 days per week
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