Lead Clinical Research Coordinator

We have a great remote opportunity for a Lead Clinical Research Coordinator. Applicants can apply here: https://www.curebase.com/career/4540898003?gh_jid=4540898003

We're particularly interested in people who meet the below Job Description from our website:

Lead Clinical Research Coordinator
at Curebase (View all jobs)
U.S - REMOTE


Job Description:

Curebase, Inc is looking for a Lead Clinical Research Coordinator to join our expanding team. As a Lead Clinical Research Coordinator Coordinator you will be responsible for the following:



- Perform duties for assigned clinical study(ies) as delegated by the Principal Investigator
- Conduct study activities (e.g., conducting the consent process and the recording and management of study data, virtual visits, randomization, follow up)
- Interact with study subjects via multiple remote venues (e.g., phone, email, text, chat)
- Function as subjects’ primary point of contact and facilitate involvement of other study team members, as needed (e.g., notify Principal Investigator of safety events)
- Manage subject visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s)
- Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal Investigator
- Request, obtain, and review subjects’ medical records
- Transcribe information from source documents (e.g., medical records) into the EDC
- Maintain regular contact with the Principal Investigator and site team to review study details (e.g., progress, adverse events, enrollment)
- Facilitate shipment of study supplies to subjects and issue appropriate study stipends
- Remain available for meetings with the study monitors, auditors, and investigators
- Ensure timely response to queries and documentation of study-related issues
- Supervise other coordinators for assigned clinical study(ies)
- Answer team members’ questions, assist with issues, and oversee work for quality and compliance
- Develop strategies, processes, and organizational tools for clinical studies
- Conduct team meetings to provide updates on best practices and expectations
- Hire, train, and mentor research coordinators


Job Requirements:

Candidates must have the following experience/qualifications:



- High school degree or equivalent required. Bachelor’s degree in biology, clinical research, nursing, or related field preferred.
- Minimum of two years’ experience in a clinical research environment, including a minimum of one year working across multiple protocols
- Must be qualified by education, training, and experience to perform any tasks delegated to him/her by the Principal Investigator
- Tech-savvy with the skills and ability to apply new systems to her/his everyday tasks
- Understand the importance of adaptability and eagerness to learn and adapt to technology changes over time
- Recent (within the last three years) training in good clinical practice
- Working knowledge of ICH-GCP, US CFR, and HIPAA regulations
- Leadership and organizational abilities
- Strategic thinking and problem-solving aptitude
- Exceptional team management skills
- Excellent verbal and written communication
- Ability to delegate effectively