850 senior clinical research coordinator jobs found

Senior Clinical Research Coordinator – Oxnard, CA HealthCare Support is actively seeking a Senior Clinical Research Coordinator to fill a job opening. This role’s location is in Chicago, IL (this role may periodically require travel to a secondary site to provide support or temporary coverage as needed). Daily Responsibilities for Senior Clinical Research Coordinator: Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants) Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol Creates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulations Contributes to the training of clinical trial staff and accountable for compliance with the...

Duration: 12 Months (Possibility of extension) Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the Principal Investigator, the Sr. CRC is responsible for the oversight, facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The Sr. CRC works collaboratively with the entire team, sponsors, and Clinical Quality Associates to ensure productivity, quality, and timely completion of studies. The Sr. CRC is expected to support, guide, train, demonstrate and lead clinical trial team members in the implementation of trial related activities. The Sr. CRC applies critical thinking and creative problem-solving skills across a wide variety of clinical...

Duration: 12 Months Job Description: This position is entirely an on-site CRC role requiring daily travel to a primary site. This role may periodically require travel to a secondary site to provide support or temporary coverage as needed. Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously. Demonstrated ability to work independently, make informed decisions, and drive clinical trials forward Track record of managing multiple clinical trials simultaneously with meticulous attention to detail Strong prioritization skills, adept at meeting deadlines, and flexible in adapting...

Duration: 12 Months Job Description: This position is entirely an on-site CRC role requiring daily travel to a primary site. This role may periodically require travel to a secondary site to provide support or temporary coverage as needed. Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously. Demonstrated ability to work independently, make informed decisions, and drive clinical trials forward Track record of managing multiple clinical trials simultaneously with meticulous attention to detail Strong prioritization skills, adept at meeting deadlines, and flexible in...

Job Title: Senior Clinical Research Coordinator Job Description 5+ years of experience coordinating Clinical Research trials Working to help enroll patients in clinical trials via pharmacy locations 5 days on-site. Must have phlebotomy proficiency Must have knowledge of regulatory affairs--able to work independently as the primary/sole Clinical Research professional onsite Excellent patient/customer service skills Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants). Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol. Creates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulations. Contributes to the training of...

Job Title: Senior Clinical Research Coordinator 100% ONSITE role, 2 locations available In Las Vegas, NV North Las Vegas Zip: 89032 Last Vegas Zip: 89146 Job Description 5-10 years of experience coordinating Clinical Research trials Working to help enroll patients in clinical trials via pharmacy locations 5 days on-site. Must have phlebotomy proficiency Must have knowledge of regulatory affairs--able to work independently as the primary/sole Clinical Research professional onsite Excellent patient/customer service skills Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants). Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol. Creates standard operating procedures (SOPs) that adhere to all Food and...

Job Title: Senior Clinical Research Coordinator 100% ONSITE role, 3 locations available: River Forest Oak Park Chicago Job Description 5+ years of experience coordinating Clinical Research trials Working to help enroll patients in clinical trials via pharmacy locations 5 days on-site. Must have phlebotomy proficiency Must have knowledge of regulatory affairs--able to work independently as the primary/sole Clinical Research professional onsite Excellent patient/customer service skills Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants). Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol. Creates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office...

Duration: 12 Months (Possibility of extension) Job Description: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. Working in collaboration with the Principal Investigator, the Sr. CRC is responsible for the oversight, facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The Sr. CRC works collaboratively with the entire team, sponsors, and Clinical Quality Associates to ensure productivity, quality, and timely completion of studies. The Sr. CRC is expected to support, guide, train, demonstrate and lead clinical trial team members in the implementation of trial related activities. The Sr. CRC applies critical thinking and creative problem-solving skills across a wide variety of clinical...

Job Summary Physicians Research Group is seeking a highly skilled and experienced Senior Clinical Research Coordinator to join our dynamic team. The Senior Clinical Research Coordinator will oversee and coordinate all aspects of clinical trials, ensuring compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols. The ideal candidate will have strong leadership skills, an in-depth understanding of clinical trial processes, and the ability to manage complex studies from initiation to completion. Key Responsibilities: 1. Study Management and Coordination - Oversee and manage the day-to-day operations of multiple clinical trials, ensuring that all studies are conducted according to the protocol, GCP, and regulatory requirements. - Develop and maintain detailed study documentation, including protocols, informed consent forms, and case report forms. - Ensure accurate and timely data collection, entry, and reporting...

Scheduled Hours 40 Position Summary Position oversees and coordinates complex and/or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; may supervise clinical research staff. Position supports several PIs and provides oversight to research scholars and trainees’ studies. Job Description Primary Duties & Responsibilities: Primary liaison to PI in developing plans for research projects and discussing the interpretation of results; collaborates in the preparation of manuscripts for publication and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate. Responsible for the development of forms, questionnaires and the application of research techniques; assists in writing...

Join a thriving boutique clinical organisation that has experienced healthy growth and is looking to expand its team. This is a fantastic opportunity to work in a close-knit environment where collaboration and a healthy work-life balance are prioritised. As a Senior Clinical Research Coordinator, you will be responsible for the full end-to-end management of multiple projects. You will have access to a range of trials and so will have a good variety of work. This role will be an initial 12-month contract, looking to transfer to a permanent position at the end of the tenure. Key Responsibilities: Coordinate and oversee all aspects of clinical research studies, ensuring compliance with protocols, regulations, and ethical guidelines. Recruit, screen, and enrol eligible study participants while maintaining accurate documentation and informed consent. Schedule and conduct study visits, procedures, and follow-up assessments according to study protocols....

University of Colorado Anschutz Medical Campus School of Medicine | Department of Biomedical Informatics Job Title: Qualitative & Mixed Methods Researcher (Entry – Senior Level) Position: #00827053 – Requisition: #34876 Job Summary: We are seeking an enthusiastic and dedicated qualitative and mixed methods researcher to join the Claw Indigenous Genomics and Ethics Laboratory (Claw lab), under the supervision of Katrina Claw, PhD, located in the Department of Biomedical Informatics at the University of Colorado Anschutz Medical Campus. The Claw lab focuses on pharmacogenomics and the cultural, ethical, legal, and social (CELSI) implications of genomic research with American Indian/Alaska Native and other Indigenous communities. Current research in the lab focuses on examining perspectives of genetic research, data sharing, inclusion and equity, and other ethical issues in Indigenous communities and historically underrepresented groups. More broadly, the CU...

University of Colorado Anschutz Medical Campus Department: Clinical Research Support Team (CReST) Job Title: Clinical Research Point Coordinator Position #: 00827546 – Requisition #: 34892 Job Summary: The Clinical Research Support Team (CReST) has an opening for a full-time Intermediate Clinical Research Point Coordinator to provide regulatory, study coordination, and data collection/entry support for a variety of drug, device and biologic studies conducted at the University of Colorado Anschutz Medical Campus and affiliate hospitals. This position may act as lead or co-lead coordinator overseeing coordinating activities for assigned studies, and/or as a primary contact for training and guidance for junior coordinators supporting these studies. This position will have independent decision making and project management responsibilities. Knowledge of Good Clinical Practice and Good Documentation Practices in the context of clinical research is essential. We are...

Job Description - Area Program Manager - Special Investigations Unit (240007RT) Job Description Area Program Manager - Special Investigations Unit - (240007RT) Description The Department of Children and Families (DCF) is seeking a dynamic, highly organized, mission-driven individual to fill the role of Area Program Manager (APM) for the Special Investigations Unit (SIU). The Special Investigations Unit is based out of Central Office, is a dedicated and centralized Intake and Investigations program that conducts statewide screening and investigations of abuse and neglect allegations concerning children in licensed residential programs, daycare, foster/adoptive homes, and other institutions, including allegations involving DCF employees and specific community stakeholders. The Area Program Manager is a member of the SIU senior management team, is involved with all aspects of the daily activities of the clinical staff, and reports to the Special Investigations Director. The...

Full job description The Department of Children and Families (DCF) is seeking a dynamic, highly organized, mission-driven individual to fill the role of Area Program Manager (APM) for the Special Investigations Unit (SIU). The Special Investigations Unit is based out of Central Office, is a dedicated and centralized Intake and Investigations program that conducts statewide screening and investigations of abuse and neglect allegations concerning children in licensed residential programs, daycare, foster/adoptive homes, and other institutions, including allegations involving DCF employees and specific community stakeholders. The Area Program Manager is a member of the SIU senior management team, is involved with all aspects of the daily activities of the clinical staff, and reports to the Special Investigations Director. The selected candidate will provide supervision to SIU supervisors and any other specialty positions as assigned. Such supervision would include...

Full job description Position Location Fort Collins, CO Work Location Position qualifies for hybrid/in-office work Research Professional Position No Posting Number 202401615AP Position Type Admin Professional/ Research Professional Classification Title Research Associate III Number of Vacancies Work Hours/Week 40 Proposed Annual Salary Range $70,000 - $115,000 Employee Benefits Colorado State University is not just a workplace; it’s a...

Full job description Research Faculty Description University of Colorado Anschutz Medical Campus Department: Biomedical Informatics Job Title: Open Rank- Research Instructor, Sr. Research Instructor Position #00826395: – Requisition #:34874 Job Summary: The University of Colorado Cancer Center is seeking a bioinformatics researcher with experience in one or more of these areas: bioinformatics analysis, algorithm development, and/or pipeline development and application. The ideal candidate will have applied or developed bioinformatics methods applicable to cancer research in at least one, but preferably several -omics types. We have particular interest in individuals with expertise in bulk and/or single cell transcriptomics. This position will be part of a team of highly experienced bioinformatics analysts that work across an array of -omics technologies. The ideal...

Posting Number: req20579 Department: Senior VP Health Sciences Location: University of Arizona Health Sciences Address: Tucson, AZ USA Position Highlights University of Arizona Health Sciences (UAHS) Research Administration invites applicants for the position of Activation & Data Coordinator. A successful candidate is responsible for the routing and tracking of contracting projects for Research Administration's research contracts team and providing project coordinator services throughout the life of each project. They will work closely with faculty, research nurses, study teams, and our medical partner, Banner Health, to provide timely and expert support in the administrative routing and maintenance of contracts. Outstanding UA benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the...

Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com, then access Find Jobs from the Workday search bar to view and apply for open positions. Students at University of Arkansas System two-year institutions will also view open positions and apply within Workday by searching for “Find Jobs for Students”. All Job Postings will close at 12:01 a.m. CT on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application process will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page. Closing Date: 09/26/2024 Type of Position: Clinical Staff - Clinical Support Job Type: Regular Work Shift: Sponsorship Available: No Institution Name: University of Arkansas for Medical Sciences The University of Arkansas for...

IT Senior Professional - 34851 University Staff Description University of Colorado Anschutz Medical Campus Department of Pathology IT Senior Professional Position # 00802794 – Requisition #:34851 Job Summary: This position works within the Department of Pathology Informatics Team to provide clinical desktop management support, maintain the stability of overall departmental network, computers, software, and related components with respect to clinical, technical, administrative clinical goals. Responsibilities of the position include clinical faculty and technical staff desktop support, user training, software and hardware upgrades and maintenance, disaster recovery, and data security. The position involves constant communication with faculty, residents, technicians, and clinical staff of the University of Colorado Denver campus and Children's Hospital Colorado. Key Responsibilities: Hardware Configuration and Maintenance – 10%...

Research Services Professional (Open Rank: Entry – Principal) - 34842 University Staff Description University of Colorado Anschutz Medical Campus Department: Biochemistry & Molecular Genetics Job Title: Research Services Professional (Open Rank: Entry – Principal) Position # 00827369 – Requisition #: 34842 Job Summary: The primary duties of this full time position will be to perform molecular biology, biochemistry and/or structural biology, and cell culture experiments designed to elucidate the molecular mechanisms of pre-mRNA splicing and its role in disease, as well as the structure and function of the Six1/Eya transcriptional complex for anti-cancer drug design. Key responsibilities: Molecular biology experiments including sub-cloning and mutagenesis Protein and/or RNA expression and purification Biochemical and biophysical analyses of protein/protein interaction and/or enzyme function Mammalian cell culture experiments...

Grants & Contracts Coordinator - 32934 University Staff Description University of Colorado Anschutz Medical Campus Department: Anesthesiology Job Title: Grants & Contracts Coordinator (Open Rank: Intermediate – Senior) Position #00796104 – Requisition #32934 Job Summary: This Grants & Contracts Coordinator in the Department of Anesthesiology will support research faculty and staff by providing comprehensive financial management for all Anesthesia research programs (federal, industry, institutional, and departmental-sponsored projects) and providing support with grant submissions and contract execution. Additional functions of this position will also include monitoring activities and preparing invoices; processing financial activities in CU systems; monthly reconciliations of expenditures and revenues on a per-project basis, and performing all other duties and tasks as required and/or assigned. This position will be held accountable for...

Office Supervisor - Multi-Specialty Medicine, Highlands Ranch University of Colorado Denver Office Supervisor - Multi-Specialty Medicine, Highlands Ranch - 34848 University Staff Description University of Colorado Anschutz Medical Campus Department: Community Practice Job Title: Office Supervisor - Multi-Specialty Medicine, Highlands Ranch Position #: 00796521 - Requisition #:34848 Job Summary: The Office Supervisor coordinates activities with the Practice Manager to ensure efficient, cost-effective business operations of the practice on a day-to-day basis by performing a variety of tasks. Collaborates with the Practice Manager and physicians to facilitate exceptional customer service. The Office Supervisor collaborates with the Practice Manager to plan, organize, communicate, coordinate, administer, teach, and evaluate nonclinical staff in their service to patients. The Office Supervisor contributes to the growth of the medical practice by promoting...

Human Resources Professional Open Rank Intermediate/Senior - 34838 University Staff Description University of Colorado Anschutz Medical Campus Department: Adult and Child Center for Outcomes Research and Delivery Science Job Title: Human Resources Professional Open Rank Intermediate/Senior Position: # TBD 00827315 – Requisition: # 34838 Job Summary: The Adult and Child Center for Outcomes Research and Delivery Science (ACCORDS) is looking for a part-time (.50 FTE) enterprising HR Coordinator who can assist in expanding our HR support and services. This position does have the potential to increase FTE over time. The Human Resources Coordinator is responsible for supporting the day-to-day transactional functions of human resources for the Adult and Child Center for Outcomes Research and Delivery Science (ACCORDS) within the School of Medicine. This role assists the ACCORDS Human Resource Program Manager and specifically handles HR transactions,...