IQVIA is looking to solve the problem of conducting clinical research studies efficiently and effectively, ensuring the well-being of subjects and maintaining high standards of clinical research practices.
Requirements
- 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.
- Skill in carrying out required clinical procedures.
- Working knowledge of medical terminology.
- Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
- Phlebotomy certification
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.
- Update and maintain skills, training, and knowledge of current best nursing practices and topics related to clinical research.
- 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.
- 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
- High School Diploma and 1 years’ relevant work experience in clinical research
- At least 1 year experience working in a clinical research setting preferred.
- Ability to pay close attention to detail.
- Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
- Please note, this position is not eligible for sponsorship.
