A company is looking for a Virtual Clinical Research Coordinator.Key Responsibilities : Collaborate with research staff to identify, recruit, and enroll eligible patients for clinical trials virtuallyCollect, maintain, and store all relevant data associated with clinical research trialsInteract with potential participants to educate them regarding clinical research trials and participant requirements to obtain proper informed consentRequired Qualifications : Bachelor's degree or RNMinimum three years of experience in clinical research as a research coordinator related to medical devices, drugs, and / or biologicsExperience with all clinical trial activities within a decentralized clinical trial structure is highly preferredCurrent certification from a research-related accredited program such as The Association of Clinical Research Professionals (CCRC or similar) is preferredKnowledge and experience utilizing research evidence and providing statistical analysis is advantageous
Senior Clinical Research Coordinator
Unblinded Lead Clinical Research Coordinator. Clinical Research Coordinator experience including Unblinded experience. Tekton Research is a growth-oriented research company focused on excellent conduct of clinical trials. Investigational Product (IP) for clinical research trials. ...
Clinical Research Coordinator
Clinical Research Coordinator II. Experienced Clinical Research Coordinator / ACRC TRIALS. Thorough knowledge of medical research. ...
Clinical Research Coordinator I, Pediatrics
The Pediatrics Department is currently seeking a qualified candidate to fill the role of Clinical Research Coordinator II within the Pediatrics Research Administration team. The ideal candidate will play a pivotal role in the collection and meticulous quality control of clinical or basic research da...
Unblinded Clinical Research Coordinator III
Unblinded Clinical Research Coordinator III Unblinded CRC III will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Any other duties/ tasks assigned by the manager KNOWLEDGE & EXPERIENCE Education: High School Diploma or equivalent required Foreign...
Clinical Research Coordinator Bleeding Disorders
The Clinical Research Coordinator may coordinate device and drug treatment research trials, as well as observational studies conducted at Children's Medical Center, including but not limited to study set-up, implementation, fiscal monitoring, and data collection/entry. Consult with Children's Medica...
Clinical Research Coordinator
The Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementation through study closure per federal, state and Institutional guidelines. Implements various protoc...
Clinical Research Coordinator II
Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the 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. ...
Clinical Research Coordinator - Oncology
Clinical Research Coordinator - Oncology (Plano Study Coordinator). Our Plano campus is looking for an experienced Clinical Research Coordinator who will play an important part in coordinating drug treatment research trials within the Hematology and Oncology teams, as well as observational studies. ...
Clinical Research Coordinator
Provides assistance to practice manager, clinical coordinator, mid-level providers, and physicians as related to drug study responsibilities. At least two years experience in a clinical research setting preferred. Performs all aspects of research related job duties in accordance with site-specific s...
Clinical Research Coordinator III
Occasionally attending out-of-town Investigator Meetings Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent Facilitate ef...