IQVIA is looking to hire a Clinical Research Coordinator to support clinical research studies, ensuring the well-being of subjects and adherence to protocols and GCP guidelines.
Requirements
- Phlebotomy is required, and pediatric experience is also needed.
- Skill in carrying out required clinical procedures.
- Working knowledge of clinical trials.
- Working knowledge of the principles of Good Clinical Practices (GCP).
- In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
- Working knowledge of medical terminology.
- Ability to pay close attention to detail.
Responsibilities
- Perform a variety of complex clinical procedures on subjects including but not limited to ECG, sample collection including spirometry, and vital signs.
- Coordinate clinical research studies conducted by a supervising principal investigator.
- Reviewing the study protocol, case report form (CRF), other study documents, and electronic data capture systems.
- Performing clinical set-up and preparation for the study including labeling specimen collection tubes and containers, setting up equipment and documents.
- Assisting with data quality checking and query resolution to ensure that data collected on study volunteers adhere to study protocol and ensuring quality control for content accuracy and completeness.
- Collecting, recording, and reporting clinical data and findings appropriately in case report forms (CRFs).
- Following ICH GCP guidelines with regards to all study and patient activities.
Other
- community outreach will be part of the role.
- Update and maintain skills, training, and knowledge of current best nursing practices and topics related to clinical research.
- Maintain a safe environment in accordance with Health and Safety policies.
- Act as a volunteer advocate.
- Equivalent education and experience - High School Diploma and 1 years’ relevant work experience in clinical research
