
Clinical Research Coordinator
Há 9 horas
Job Overview:
We are seeking a highly skilled and motivated Clinical Research Coordinator to join our team. In this role, you will be responsible for performing tasks associated with site activation in accordance with local and international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines.
- You will serve as the Single Point of Contact (SPOC) for investigative sites, ensuring adherence to SOPs, Work Instructions (WIs), quality of deliverables, and project timelines.
- You will perform start-up and site activation activities according to applicable regulations, SOPs, and work instructions.
- You will prepare site regulatory documents, reviewing for completeness and accuracy.
- You will maintain accurate completion and up-to-date information in internal systems, databases, and tracking tools.
- You will review and provide feedback on site performance metrics.
- You will establish and agree on project planning and timelines, ensuring monitoring measures are in place and contingency plans are implemented as needed.
- You will inform team members of completed regulatory and contractual documents for individual sites.
- You will review, track, and follow up on the progress, approval, and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.
- You will provide local expertise to Site Activation Managers and project teams during initial and ongoing project timeline planning.
- You will perform quality control of documents provided by sites.
- 1 year of clinical research experience or an equivalent combination of education, training, and experience.
In this role, you will have the opportunity to develop your skills and knowledge in clinical research coordination, working closely with a team of experienced professionals.
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