Travel Clinical Research Associate
Abarca Health- Full Time
- Junior (1 to 2 years)
Candidates should possess a Bachelor’s degree, which is preferred, and one year of experience in the pharmaceutical industry or other relevant experience is required. Strong problem-solving and organizational skills are necessary, along with demonstrated ability to manage multiple tasks simultaneously and complete work within allocated time frames. Excellent oral and written communication skills, including fluency in English, are also required.
The Associate Clinical Data Reviewer will ensure the accuracy of client data by conducting manual data review for Clinical Data Management customers, issuing queries based on manual data review requirements, participating in project team meetings, generating metrics and reports, and performing user acceptance testing. They will also adhere to Clinical Data Management processes and standards, read and understand SOPs, and contribute to team efforts by resolving issues and exploring new opportunities. Additionally, they will maintain technical and industry knowledge through training and perform other duties as assigned, while adhering to company policies and SOPs.
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.