DataPharma
DataPharma is a company focused on leveraging data analytics and digital solutions to enhance the pharmaceutical industry. They aim to optimize drug development processes, improve patient outcomes, and streamline operations within healthcare. With an emphasis on data-driven decision-making, DataPharma is positioned to impact various sectors related to pharmaceuticals and healthcare.
Clinical Research Associate II
5 days ago
DataPharma
DataPharma is a company focused on leveraging data analytics and digital solutions to enhance the pharmaceutical industry. They aim to optimize drug development processes, improve patient outcomes, and streamline operations within healthcare. With an emphasis on data-driven decision-making, DataPharma is positioned to impact various sectors related to pharmaceuticals and healthcare.
📋 Description
• Conduct site visits, including site selection, initiation, routine monitoring, and close-out visits, ensuring compliance with ICH-GCP, study protocols, and regulatory requirements. • Monitor patient safety, data integrity, and protocol adherence, identifying and resolving issues proactively. • Ensure that investigational sites maintain accurate study documentation and adhere to Good Documentation Practices (GDP). • Work across sponsor-dedicated and multi-sponsor studies, managing multiple protocols and therapeutic areas. • Provide training and support to site staff on study procedures and protocol compliance. • Review and verify case report forms (CRFs) and electronic data capture (EDC) systems for data accuracy and completeness. • Maintain effective communication with investigators, site staff, sponsors, and internal teams to ensure study timelines are met. • Assist in the resolution of site-specific issues, queries, and deviations, escalating as necessary. • Support in ethics submissions, regulatory documentation, and site feasibility assessments where required. • Contribute to continuous process improvement and ensure adherence to SOPs and company policies.
🎯 Requirements
• Minimum of 2 years’ independent monitoring experience in clinical research. • Strong understanding of ICH-GCP, regulatory guidelines, and clinical trial operations. • Experience in both sponsor-dedicated and multi-sponsor settings is preferred. • Ability to manage multiple sites and protocols across different therapeutic areas. • Excellent communication, problem-solving, and relationship-building skills. • Ability to travel as required for site monitoring visits. • Degree in Life Sciences, Pharmacy, Nursing, or a related field.
Apply NowSimilar Jobs
March 5
Clinical Research Associate role at Parexel, focused on delivering healthcare solutions in Turkey.
Discover 100,000+ Remote Jobs!
Wall of Love
Frequently asked questions
We use powerful scraping tech to scan the internet for thousands of remote jobs daily. It operates 24/7 and costs us to operate, so we charge for access to keep the site running.
Of course! You can cancel your subscription at any time with no hidden fees or penalties. Once canceled, you’ll still have access until the end of your current billing period.
Other job boards only have jobs from companies that pay to post. This means that you miss out on jobs from companies that don't want to pay. On the other hand, Remote Rocketship scrapes the internet for jobs and doesn't accept payments from companies. This means we have thousands more jobs!
New jobs are constantly being posted. We check each company website every day to ensure we have the most up-to-date job listings.
Yes! We’re always looking to expand our listings and appreciate any suggestions from our community. Just send an email to Lior@remoterocketship.com. I read every request.
Remote Rocketship is a solo project by me, Lior Neu-ner. I built this website for my wife when she was looking for a job! She was having a hard time finding remote jobs, so I decided to build her a tool that would search the internet for her.