Clinical Research Assistant II - Psychiatry & SOAR Study
The Ohio State University
The Ohio State University Medicine | Psychiatry is seeking a Clinical Research Assistant II to support the SOAR initiative. You will assist in recruitment and consent, and perform behavioral or diagnostic testing according to study protocols. You will process biospecimens, collect biometric data, and maintain and report study data. The role is a fixed-term, full-time position with varying shifts in a collaborative research environment. #J-18808-Ljbffr The Ohio State University
- Job Title: Clinical Research Assistant II-Psychiatry Department: Medicine | Psychiatry To aid in support of clinical research... ...of Ohio Adversity and Resilience (SOAR) initiative. SOAR is a state of the art, multigenerational study of family/ household units that focuses...SuggestedFixed term contractShift work
- ...Experienced Clinical Research Associate II -Sponsored Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built... ...software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic...SuggestedInterim roleLocal areaImmediate startRemote work
- Worldwide Clinical Trials in the United States seeks an In-house Clinical Research Associate II to manage sites and ensure compliance with GCPs and SOPs. You will support CTMs... ...monitoring visits, data review, and timely study deliverables. A four-year science degree and...SuggestedWorldwide
$50k - $99k
...excellence. We are Worldwide Clinical Trials, and we are a global... ...What the In-House Clinical Research Associate II does at Worldwide Clinical Trials... ...site management tasks for studies in accordance with Good... ...oversight. What you will do Assist with feasibility questionnaires...SuggestedHourly payInterim roleWork at officeLocal areaRemote workWorldwide- Worldwide Clinical Trials is seeking an In-house Clinical Research Associate II to manage sites for CNS/Neurology studies, ensuring adherence to GCPs and regulatory requirements. The role provides support to CTMs and field CRAs, with mentorship to junior staff. The candidate...SuggestedWorldwide
- Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA ICON plc is a... ...leading healthcare intelligence and clinical research organization. We’re proud to foster an... ...for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour...Work experience placementWork at officeWork from homeFlexible hours
- Worldwide Clinical Trials is seeking an In-house Clinical Research Associate II to manage sites per GCPs and SOPs. You will support CTMs and field CRAs while mentoring in-house staff, ensuring timely deliverables across trials. The role requires at least two years of clinical...Worldwide
- ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Clinical Study Specialist for a hybrid role in the US. The role involves organizing reports, coordinating meetings, and supporting TMF/CTMS processes across global trials. You...
- ProPharma is seeking a Clinical Project Specialist to provide administrative and project management support for assigned clinical studies, coordinating with study teams to ensure compliant and timely execution. The role involves document development, tracking, site materials...
$15 - $19 per hour
...Posting Information Department: Psychiatry - Research - 412250 Career Area: Research Professionals... ...We promote health and provide superb clinical care while maintaining our strong tradition... ...of participants, conducting the study sessions, data collection and validation...Hourly payFull timeTemporary workPart timeLive inWork at officeLocal area$15 - $19 per hour
The University of North Carolina at Chapel Hill is seeking a Research Technician to support clinical trials in psychiatric disorders. This temporary position focuses on recruiting participants, conducting study sessions, data collection and validation, and preparing...Hourly payTemporary work- Creative Solutions Services, LLC seeks a Scientific - Technician II in Raleigh, NC for a 10+ month assignment. Shift is Mon-Fri 2:30pm-11pm. Responsibilities include synthesizing oligos, performing cleavages and deprotections, QC sampling, and ensuring compliance with...Shift workAfternoon shift
- ProPharma Group is seeking a Research Assistant to support remote site activities across assigned projects... ..., data-entry, and monitoring of clinical databases. You will maintain IRB/FDA-compliant documentation, assist with study closeout, and collaborate with study teams...Remote jobFlexible hours
$19 - $21 per hour
...- Cardiology - 411405 Career Area: Research Professionals Posting Open Date: 08/... ...Temporary Staff (SHRA) Position Title: Clinical Research Assistant Position Number: 20068066 Vacancy... ...consenting patients, attending off-site study meetings as required, scheduling and...Hourly payFull timeTemporary workPart timeLive inWork at officeLocal areaMonday to FridayFlexible hours- Clinical Research Associate II - Oncology (North Carolina/South Carolina) AbbVie’s mission is to discover... ...improving data integrity, compliance, study performance, and the customer... ...recommends new investigators/sites, assisting placement of studies. Ensures quality...Contract workTemporary workLocal area
- ProPharma in Raleigh, NC, is seeking a Research Assistant to support remote site activities for assigned projects, serving as the day-to-day... ...support, and ensuring IRB/FDA compliant documentation, with the study team collaboration in a hybrid work setup. A Bachelor’s...Remote job
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...support effective conduct of clinical study data review and capture, and verify site... ...Phase, act as Site Management Associate II and support site activities throughout...Interim roleLocal areaImmediate startRemote workFlexible hours
- ...domain expertise in regulatory sciences, clinical research solutions, quality & compliance,... ...management support for assigned clinical studies and projects, working closely with study... ...to clinical trial execution, including assisting with the development, formatting, review...Full timeWork at officeRemote work
- ...human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement... ...company Standard Operating Procedures (SOPs) governing clinical studies. Location: Remote, US What You Will Do: ~ Responsible...Full timeWork experience placementWork at officeRemote workShift work
- ...Clinical Research Associate For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise... ...parameters. Ex-US: May be responsible for performing study start up activities in accordance with local practice,...Interim roleWork at officeLocal areaRemote work
- Experienced Clinical Research Associate - Sponsor Dedicated Updated: Yesterday Location: Remote, NC, United States Job ID: 25109784 Description... ...software to support the effective conduct of the clinical study data review and capture. Verifies site compliance with...Interim roleLocal areaImmediate startRemote work
$100 - $112 per hour
...DOYou will utilize your skills, knowledge, and clinical judgement to provide a high standard of care... ...respond to emergency situations based upon clinical research standards.Responsibilities :Responsible for all aspects of study site monitoring including routine monitoring...Work at officeLocal areaRemote workNight shift- Emerald Clinical Trials is building a pipeline of Clinical Research Associates across the United States as we prepare for continued growth and new study awards. Join a global team focused on renal, cardiometabolic, oncology studies, with on-site monitoring, site relationship...Remote job
$97k - $193k
...quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over... ...on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find... ...Typically involved in all stages of the clinical study, including identifying potential sites to...Hourly payWork at officeRemote workWorldwide$110k - $130k
Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical... ...all phases, offering Phase I-IV and real-world studies. Who We Are Emerald Clinical Trials is a global leader...Local areaRemote workWorldwide- Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated work. The role operates remotely within the United... ...monitoring, and close-out activities in accordance with ICH-GCP and study protocol. You will verify informed consent, protect patient...Remote job
- Worldwide Clinical Trials is seeking a Senior Clinical Research Associate with CNS experience for remote work in the Southeast/Mid-Atlantic United States. The... ...training sites, and ensuring regulatory compliance across studies. Applicants should have 5+ years as a CRA, a 4-year...Remote jobWorldwide
- The Clinical Support Specialist provides critical operational and administrative... ...Start-Up Managers, Clinical Research Associates (CRAs), and cross-... ...teams to ensure clinical studies are organized, compliant, and... ...operating procedures (SOPs). Assist with study start-up...Contract workWork at office
- ...curation at scale, and modern study design to build continuous,... ...multimodal evidence that supports clinical, regulatory and strategic... ...is seeking a Senior Clinical Research Associate to conduct site management... ...all monitoring activities. Assist with site start-up activities...Work at officeRemote work
$100k - $112k
...WHAT YOU WILL DO Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of... ...management systems as assigned by management Assist with training of new employees, eg. co-monitoring...Work at officeLocal areaRemote workNight shift
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