Clinical Research Coordinator III
3 weeks ago
Job Description Job Description Clinical Research Coordinator IIIA CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.DUTIES & RESPONSIBILITIES Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:Sponsor-provided and IRB-approved Protocol TrainingAll relevant Protocol Amendments TrainingAny study-specific Manuals Training, as applicableSponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.Demonstration of appropriate and timely follow-up on the action items, at their respective sites.Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).Ability to train and mentor site staff, as neededSupervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)Demonstration of appropriate and timely follow-up on the action items, at their respective sites.Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).Maintaining a working knowledge of Study Participants Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).Being prepared for and available at all required company meetings.Submitting required administrative paperwork per company timelines.Occasionally attending out-of-town Investigator MeetingsConduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternativesProvide clear explanations of study protocols and ensure patients' understanding before obtaining their consentFacilitate effective communication between patients, healthcare providers, and research staffAny other matters as assigned by managementKNOWLEDGE & EXPERIENCEEducation: High School Diploma or equivalent requiredBachelor's degree preferredForeign Medical Graduates preferredExperience: Minimum of 5 years experience in Clinical ResearchSupervisory experience preferredWide therapeutic range of clinical trials experience preferredRegulatory research experience is a plusCredentials: ACRP or equivalent certification is preferredKnowledge and Skills: Goals-driven while continuously maintaining quality.Must be detailed-oriented, proactive, and able to take initiative.Must have strong written and communication skills.Must have excellent customer service skills.Proficient communication and comprehension skills both verbal and written in the English language are required.Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.Powered by JazzHRvgm6fRJw4m#J-18808-Ljbffr
by Jobble
-
Clinical Research Coordinator III
4 weeks ago
Oak Park, United States DM Clinical Research Full timeJob DescriptionJob DescriptionClinical Research Coordinator IIIA CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To...
-
Program Manager III
2 days ago
Menlo Park, United States Crystal Equation Full timeProgram Manager III Onsite Summary: The main function of a non-IT program manager is to plan, direct, or coordinate activities in such fields as engineering, research and development, financial systems and product roll-out, etc or any other non-IT ba Program Manager, Manager, Program, Skills, Business Services, Staffing
-
Clinical Research Patient Recruiter
1 month ago
Winter Park, United States MyKelly Full timeKelly® Science & Clinical is working with a rapidly expanding clinical research site based out of Winter Park, Florida fulfill an immediate need for a Clinical Research Patient Recruiter position. If you are interested in starting a career in clinical trial research, this is a rare and exciting opportunity with tremendous job growth!Job Description: Patient...
-
CLINICAL RESEARCH NURSE
3 weeks ago
Royal Oak, MI 48073, USA, United States psg Full timeThe Clinical Research Nurse will provide clinical support in the Cardiovascular Research clinical trials office. The Clinical Research Nurse role is the specialized practice of professional nursing focused on maintaining equilibrium between care of t Clinical, Research, Nurse, Healthcare, Staffing, Activities
-
Education Quality Coordinator Rn
4 weeks ago
Oak Park, United States RUSH Oak Park Hospital Full time**Education Quality Coordinator RN** **Location**:Oak Park, IL **Hospital**:RUSH Oak Park Hospital **Department**: Operating Room **Work Type**: Full Time (Total FTE between 0. 9 and 1. 0) **Shift: Shift 1** **Work Schedule**:8 Hr (8:00:00 AM - 4:03:00 PM) Summary: The Education Quality Coordinator (EQC) is an experienced nurse who coordinates and...
-
Clinical Research Patient Recruiter
2 weeks ago
Winter Park, United States SQRL Full timeOpportunity to join the Patient Recruitment Team of one of the fast-growing clinical research companies within the Winter Park, FL area! Great full-time position for Pre-Med students or those wanting to break into the Clinical Research industry! HighlightsPlay a major role in helping patients get involved in cutting-edge clinical trials - a meaningful...
-
Clinical Research Patient Recruiter
5 days ago
Winter Park, United States SQRL Full timeOpportunity to join the Patient Recruitment Team of one of the fast-growing clinical research companies within the Winter Park, FL area! Great full-time position for Pre-Med students or those wanting to break into the Clinical Research industry! HighlightsPlay a major role in helping patients get involved in cutting-edge clinical trials - a meaningful...
-
Executive Administrative Coordinator
5 days ago
Oak Park, United States Mack & Associates, Ltd. Full timeA reputable non-profit organization nestled in the vibrant community of Oak Park, Illinois, is eagerly seeking an exceptional Executive Administrative Coordinator to join their dedicated team. In this pivotal role, you'll provide crucial administrative support to the esteemed CEO and HR Director, ensuring the seamless operation of all organizational...
-
Executive Administrative Coordinator
5 days ago
Oak Park, United States Mack & Associates, Ltd. Full timeA reputable non-profit organization nestled in the vibrant community of Oak Park, Illinois, is eagerly seeking an exceptional Executive Administrative Coordinator to join their dedicated team. In this pivotal role, you'll provide crucial administrative support to the esteemed CEO and HR Director, ensuring the seamless operation of all organizational...
-
Executive Administrative Coordinator
2 days ago
Oak Park, United States Mack & Associates, Ltd. Full timeA reputable non-profit organization nestled in the vibrant community of Oak Park, Illinois, is eagerly seeking an exceptional Executive Administrative Coordinator to join their dedicated team. In this pivotal role, you'll provide crucial administrative support to the esteemed CEO and HR Director, ensuring the seamless operation of all organizational...
-
CLINICAL RESEARCH NURSE SR
3 weeks ago
Royal Oak, MI 48073, USA, United States psg Full timeThe Regulatory Clinical Research Nurse Sr. provides regulatory support and expertise for various research departments. The Research Nurse Clinician (RNC) role is the specialized practice of professional nursing focused on maintaining equilibrium betw Clinical, Research, Nurse, Clinician, Regulatory, Healthcare, Staffing
-
Executive Administrative Coordinator
4 weeks ago
Oak Park, United States Oak Park Residence Corporation Full timeJob DescriptionJob DescriptionTITLE: Executive Administrative CoordinatorPRIMARY RESPONSIBILITY: To provide high level administrative and project support to CEO and Director of HR. To coordinate and/or perform a diverse set of administrative functions, projects, and support tasks to ensure the organization has the resources needed to operate smoothly and...
-
Clinical Research Associate Intern
3 days ago
Brooklyn Park, United States CVRx Full timeJob DescriptionJob DescriptionWhy work for CVRx?CVRx pioneers' unique therapies that harness and harmonize the body’s natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration and purpose. If our culture and values...
-
Oak Park, Illinois, United States Motlow State Community College Full timeTitle: Assistant Professor Dental Hygiene10M_Clinical CoordinatorEmployee Classification: FacultyInstitution: Roane State Community CollegeDepartment: Health SciencesCampus Location: Roane State Community CollegeJob SummaryPosition is a faculty position as defined by PA-24-01 and includes fulfilling the duties and responsibilities of faculty in relationship...
-
Oak Park, United States Rush University System for Health Full timeRush University Medical Center, a nationally recognized clinical and academic institution, and the teaching hospital for Rush Medical and Nursing Colleges, located in downtown Chicago, invites applications for the position of General/Non-invasive Cardiologist.This position will be primarily based at Rush Oak Park Hospital in Oak Park, IL.Qualified candidates...
-
College Park, United States Axiom Consultants Full timeJob DescriptionJob DescriptionAxiom is seeking a Training and Research Meteorologist for International Desks to support the Weather Prediction Center (WPC) of the National Centers for Environmental Prediction (NCEP). The position will be based at the WPC in College Park, MD, within the NOAA Center for Weather and Climate Prediction (NCWCP). The NCWCP is a...
-
Meteorologist - Training and Research for
1 month ago
College Park, United States Axiom Consultants, Inc. Full timeAreas of particular need and interest to be addressed include the forecasting of heavy precipitation associated with tropical cyclones, warm-season convection, and atmospheric rivers. Additional areas of focus include the use of ensemble model output and forecaster generation of probabilistic products, as well as exploring future roles of weather...
-
Clinical Research Technician I.
4 weeks ago
Overland Park, United States Altasciences Full timeResponsibilities of the Clinical Research Technician I include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors is respected. Understand protocol...
-
Patient Services Coordinator
12 hours ago
Oak Park, United States CORA Physical Therapy Full timePatient Services Coordinator - Full-Time As a Patient Services Coordinator, you'll be a vital part of our clinic support team by providing meaningful patient interactions and exceptional customer service. You'll perform a wide range of administrative tasks at the front desk of a dynamic therapy office, and above all, you'll help create a great first...
-
Patient Services Coordinator
21 hours ago
Oak Park, United States CORA Physical Therapy Full timePatient Services Coordinator - Full-Time As a Patient Services Coordinator, you'll be a vital part of our clinic support team by providing meaningful patient interactions and exceptional customer service. You'll perform a wide range of administrative tasks at the front desk of a dynamic therapy office, and above all, you'll help create a great first...