Senior Clinical Project Manager
Abarca Health- Full Time
- Senior (5 to 8 years)
Candidates should possess a High School Graduate or Associate/Bachelor’s Degree in bioscience, computer science, information technology, or a related field. They must demonstrate experience coordinating site and operational activities during clinical trials, including preparation of study materials, follow-up on documentations, and scheduling logistical and technical trainings. Strong data management skills, particularly in IQC data review, tracking, and submission, are essential, along with the ability to investigate and resolve data discrepancies and manage site communications. Familiarity with software used for IQC data production and collection, such as study databases and reading analysis systems, is also required.
The Imaging Research Associate I coordinates all site and operational activities from study start to close, ensuring timely delivery of high-quality service deliverables for assigned studies. This includes assisting in study material preparation, following up on site documentation, scheduling training, reviewing and processing study data, managing site communications, and generating reports. They also perform IQC activities such as baseline, on-going, and end/interim data review, coordinating cross-calibration phantom rotation, and ensuring accuracy of tracking information. Furthermore, the role involves assisting project managers with project administration, maintaining project timelines, and addressing data queries. Finally, the associate contributes to machine equivalence analysis, manages machine change instances, and ensures IQC data is collected and maintained according to SOPs and study protocols.
Generates clinical evidence for trials
Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.