Associate Director, Quality Assurance (Clinical Research Preferred) IQVIAAssociate Director, Quality Assurance (Clinical Research Preferred)Durham, IndianaInfluence quality outcomes across multiple functional areas, business units, and customer engagements through expert guidance, risk-based decision making, and oversight of quality systems and compliance programs. Provide strategic quality leadership and oversight across assigned Quality Assurance (QA) programs, with a strong focus on clinical research, clinical operations, pharmaceutical development, and GxP-regulated activities.
Client Relationship Associate Director, Connected Devices PM (Clinical Research) IQVIAClient Relationship Associate Director, Connected Devices PM (Clinical Research)Durham, IndianaTo communicate with project teams and Business Development to ensure excellent delivery to clients and consistency across studies, including alliance and portfolio management, implementation of best practices, harmonization, and development of client-specific performance improvement projects, and to facilitate escalation management. Assist the Business Development team with RFP (request for proposal)/RFI (request for information) review for assigned accounts, working closely with the internal teams and the client.
NewClinical Research Associate Macpower Digital Assets Edge Private LimitedClinical Research AssociateResearch Triangle Park, NC$95–$105 / hourCommunicates and interacts with relevant study personnel, including developing and maintaining collaborative relationships to manage study issues and support milestone achievement; conveys project information; answers study questions in a timely manner while using discretion when to escalate to the study manager; troubleshoots and follows up on study progress; and reviews report data for completeness and accuracy. Prepares telephone contact reports, confirmation letters, site visit reports (PSV, SIV, IMV, and COV), and follow-up letters to accurately and completely document site status and activities.
Senior Clinical Research Associate ProPharma GroupSenior Clinical Research AssociateRaleigh, North CarolinaCommunicate with assigned clinical sites, investigators, site personnel, client personnel, and any other cross functional team member involved in the assigned clinical trials to address any study needs related to the monitoring and site management activities as assigned. Monitor assigned clinical trials and clinical sites by reviewing and reporting site enrollment, and termination updates, monitoring visits, protocol deviations, serious adverse events, laboratory abnormalities and any other activity at the site that contributes to proper conduct of the clinical trial per protocol, and regulatory requirements.
KBI: US - Research Associate II KBI BiopharmaKBI: US - Research Associate IIDurham, North CarolinaAssures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. Performs testing on drug substance/drug product, or formulation samples using bio-analytical techniques such as (but not limited to) HPLC, SDS-PAGE, SDS-CGE, ELISA, UV-Vis, and/or biophysical characterization techniques.
Clinical Research Associate (Level II) - FSP - Alzheimer's - Central Thermo Fisher ScientificClinical Research Associate (Level II) - FSP - Alzheimer's - CentralWilmington, North CarolinaWhat You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
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 & Central FortreaFSP Clinical Research Associate 2 - West Coast & CentralDurham, 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.
FSP 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.
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.
In Process Research Associate KBI BiopharmaIn Process Research AssociateDurham, NC$19.23–$26.44 / hourAbout KBI: KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. Assures proper labeling, handling, and storage of all chemicals used in the area, assures proper labeling and disposition of hazardous waste in satellite area; adheres to all safety requirements and follows safety procedures, and attends all required safety and health training, including handling hazardous waste.
Institutional Research and Planning Associate Southwestern Community CollegeInstitutional Research and Planning AssociateSylva, NC$45,431Collect and provide data for College Planning Activities, Program Review, annual reporting requirements, specialized program accreditation, strategic planning, IPEDS, and SACS accreditation processes. Three years of experience working strategic planning capacity with knowledge of basic data analysis methods preferred.
Research Data Associate Odyssey Systems Consulting Group, Ltd.Research Data AssociateFort Bragg, North CarolinaFull timeThe role requires proving assurance of accurate documentation in compliance with all governing regulations for the collection, validation, and analysis of TBI- relevant research and outcomes data, and incudes interaction with relevant TBI stakeholders and to elicit and document business needs when modifying existing or creating new system functionality. Position Summary: Odyssey is looking for a Research Data Associate to design, develop and implement web-based applications to support data management activities associated with clinical investigations to support the Traumatic Brain Injury Center of Excellence (TBI CoE).
Retail Inventory Associate - Research Triangle Area Retail Services WIS CorporationRetail Inventory Associate - Research Triangle AreaRALEIGH, North Carolina$16–$18 / hourPart timeRetail, stocking, merchandising, warehouse, customer service, cashier, delivery driver, gamer, athlete, coaches, and general labor experience are all valuable backgrounds for this position. Urgently hiring throughout the Research Triangle area, including Raleigh, Durham, Chapel Hill, Apex, Morrisville and Wake Forest .
Retail Inventory Associate Driver - Research Triangle Area Retail Services WIS CorporationRetail Inventory Associate Driver - Research Triangle AreaRALEIGH, North Carolina$16–$18 / hourPart timeRetail, stocking, merchandising, warehouse, customer service, cashier, delivery driver, gamer, athlete, coaches, and general labor experience are all valuable backgrounds for this position. Availability to work flexible schedules with varying hours in support of the District Manager and customer commitments, this includes very early mornings and/or late nights.
Clinical Research Associate/Pharmacy Tech. Southeastern Medical Oncology CenterClinical Research Associate/Pharmacy Tech.Goldsboro, North CarolinaManage medication transaction activities such as receiving, inspecting and reconciling investigational drug shipments, storing, labeling and dispensing, preparing for transport to satellite offices, destroying, returning and maintaining inventory accountability of investigational medications under the Clinical Trial Department Supervisor, Registered Nurse and Lead Certified Pharmacy Technician supervision. This position will handle the day-to-day operations of investigational medication management to ensure the safe handling and accurate documentation of investigational medications used in clinical research studies as well as help maintain compliance with clinical trial protocols, sponsor requirements and regulatory compliance to ensure the safe and accurate conduct of clinical research studies.
Kbi: US - Research Associate II KBI BiopharmaKbi: US - Research Associate IIDurham, NC$63,000–$80,000 / yearAssures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures, and attends all required safety and health training, including handling hazardous waste. About KBI: KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies.
Part-Time Security Associate 2nd shift Sat & Sun Research Triangle Park KPI Protection ServicesPart-Time Security Associate 2nd shift Sat & Sun Research Triangle ParkDurham, North CarolinaAs well as: Write security-related documents such as incident reports, daily reports, tracking logs. Respond to medical emergencies, bomb threats, fire alarms, or intrusion alarms following emergency response procedures.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos HealthExperienced Clinical Research Associate - Sponsor DedicatedNorth CarolinaPerforms site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan.