Remote Travel Research Specialist ExcitingtravelnowRemote Travel Research SpecialistRaleigh, North CarolinaRemoteYour role is to ensure a seamless, stress-free experience by assisting with travel arrangements, answering questions, managing updates, and resolving any challenges with professionalism and care. As a Remote Travel Research Specialist, you will be an essential part of our team, guiding clients through every stage of their journey, from the moment they plan their trip to their safe return home.
Remote Market Research Participant Up to $90/Session No Experience Required Occupons QuebecRemote Market Research Participant Up to $90/Session No Experience RequiredDurham, NORTH CAROLINARemoteYou will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.
Remote Data Entry / Online Research Panelist - Work From Home FocusGroupPanelRemote Data Entry / Online Research Panelist - Work From HomeRaleigh, NCRemoteFocusGroupPanel invites adults to join optional online research panels and focus groups from home. You choose whether to respond to each invitation and can participate using a computer, tablet, or smartphone with a reliable internet connection.
Customer Service Representative / Online Research Panelist - Remote FocusGroupPanelCustomer Service Representative / Online Research Panelist - RemoteDurham, NCRemoteFocusGroupPanel invites adults to join optional online research panels and focus groups from home. You choose whether to respond to each invitation and can participate using a computer, tablet, or smartphone with a reliable internet connection.
Lead Clinical Research Associate Actalent IncLead Clinical Research AssociateDurham, NCRemote$85–$95 / hourProvide leadership and functional oversight for monitoring teams, including Clinical Research Associates I, II, III, and senior staff, across all phases of clinical trials from start-up through enrollment, closeout, and archiving. This contract Lead Clinical Research Associate role focuses on overseeing clinical operations site management and monitoring activities for multiple trials as a 1099 contractor.
NewSr. Clinical Research Associate Actalent IncSr. Clinical Research AssociateDurham, NCRemote$85–$90 / hourThe Clinical Research Associate (CRA) will conduct onsite monitoring visits across the United States and provide comprehensive site management support for complex, high-volume cardiovascular clinical trials. Conduct onsite monitoring visits at participating study sites across the United States, ensuring compliance with the protocol, Good Clinical Practice (GCP), and applicable regulatory requirements.
Clinical Research Associate II/III - US Optimapharm ddClinical Research Associate II/III - USRaleigh, NCRemoteWith operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. As we expand our US Clinical Operations team, we're searching for a CRA II/III who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives.
Sr Clinical Research Associate Veranex IncSr Clinical Research AssociateRaleigh, NCRemoteConducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits. What You Will Do: Responsible for ensuring that study investigators and coordinators comply with the study protocol, Good Clinical Practices (GCPs), Code of Federal Regulations (CFRs), and Institutional Review Board (IRB)/Ethics Committee (EC) requirements during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions.
Senior Clinical Research Associate - US Optimapharm ddSenior Clinical Research Associate - USRaleigh, NCRemoteAt Optimapharm, you'll work on diverse and challenging studies, collaborate with experienced professionals around the world, and play a critical role in shaping the success of clinical trials - all within a culture that supports continuous growth and recognizes expertise. With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide.
Senior Clinical Research Associate ParexelSenior Clinical Research AssociateRaleigh, North CarolinaRemoteSpecial Skills or Other Requirements: Applicants must have demonstrated experience with: Serving as a Lead Clinical Research Associate (CRA) for clinical studies;Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS);Site Management and application of clinical trial methodology and terminology;Independently monitoring visits (Qualification, Site Initiation, and Monitoring);Working with clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines; andCommunicating results to stakeholders in non-technical language. Conduct, drive, and manage country-specific feasibility and site pre-qualification and qualification activities, which include preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments.
Sr Clinical Research Associate VeranexSr Clinical Research AssociateRaleigh, NCRemoteGenerates high-quality site qualification, initiation, monitoring, and close-out visit reports in timely manner (in accordance with the Clinical Monitoring Plan)Contributes to protocol, informed consent, case report form (CRF) and study plan development as well as annual progress reports (APRs) and the clinical study report (CSR) at study conclusion to report the study results to FDA and other regulatory authorities. Conducts site qualification visits, study start-up activities (essential document collection), site qualification visits, site initiation visits and training, monitoring visits for source data verification (reported study data are accurate, complete, and verifiable from source documents in the site's medical records), and site close-out visits.
NewFSP Clinical Research Associate 2 - West Coast & Texas Fortrea IncFSP Clinical Research Associate 2 - West Coast & TexasDurham, NCRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - California or Colorado Fortrea IncFSP Clinical Research Associate 2 - California or ColoradoDurham, NCRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc Fortrea IncFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncDurham, NCRemote$125,000–$140,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Clinical Research Associate Actalent IncClinical Research AssociateDurham, NCRemote$85–$90 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. The role offers a weekly workload of 40-50 hours, varying by study phase, with opportunities for hybrid work arrangements to support work-life balance.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateCary, NCRemoteICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
FSP Sr. Clinical Research Associate II - Denver, CO - Oncology FortreaFSP Sr. Clinical Research Associate II - Denver, CO - OncologyDurham, North CarolinaRemote$125,000–$140,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - West Coast & Texas FortreaFSP Clinical Research Associate 2 - West Coast & TexasDurham, North CarolinaRemote$100,000–$112,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 - California or Colorado FortreaFSP Clinical Research Associate 2 - California or ColoradoDurham, North CarolinaRemote$100,000–$112,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc FortreaFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncDurham, North CarolinaRemote$125,000–$140,000 / yearResponsibilities : Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.