Clinical Study Coordinator - 251525

Benefits

Job Description

Qualifications

• •Clinical Study CoordinatorMust Haves: Bachelors degree, 2+ years of experience in Clinical Research within the HIV area
• •Minimum QualificationsBachelor’s degree from an accredited college or university
• •Two years of experience working in a clinical research or public health setting
• •Experience with HIV patients
• •Proficiency in Microsoft Office, specifically Excel and Word
• •Understanding of the ethical/technical conduct of research or experience in public health, epidemiology, or health promotion
• •Knowledge of Good Clinical Practice (GCP) concepts.Knowledge, Skills, and AbilitiesRegulatory Knowledge: Strong understanding of HIPAA, regulatory requirements for healthcare research, and policies governing human subject research
• •Operational Skills: Ability to work independently, prioritize multiple projects, and meet deadlines in a fast-paced environment.Communication: Excellent written and oral communication skills
• •Technical Proficiency: Strong understanding of medical terminology

Benefits

• •Hours: 40 hours per week, Monday-Friday onsite, normal business hours Contract Duration: contract-to-hire, 6 month contract then have the opportunity to be hired on permanently
• •Benefits: Medical, Dental, Vision, time off, paid holidays off, 401k, growth opportunities, etc

Responsibilities

• •Working closely with the Principal Investigator, this role implements and administers study-related questionnaires, interviews, and protocol procedures
• •The position is responsible for data entry, data edits, database maintenance, and the daily operations of clinical research studies
• •Typical DutiesCoordinates and schedules participant research visits
• •Administers interviewer study questionnaires and interviews
• •Administers study-driven protocol procedures
• •Ensures the integrity of data entry, edits, and storage per protocol
• •Facilitates the collection of medical records per study protocol
• •Coordinates with the research team to facilitate timely data collection and submission
• •Manages retention efforts to keep participants on study according to the protocol visit schedule
• •Prepares shipments of dangerous goods according to IATA guidelines
• •Obtains informed consent and ensures participants understand the protocol and expectations
• •Maintains up-to-date knowledge of relevant State and Federal research guidelines
• •Performs other duties as assigned