Clinical Research Associate I & II (India)

At Allucent, you will play a crucial role in helping small-medium biopharmaceutical companies navigate the world of clinical trials to deliver life-changing therapies to patients worldwide. As a Sr. Clinical Research Associate Contractor (Sr.CRA) on our remote A-team, you will have the opportunity to independently manage and monitor investigational sites, ensuring adherence to trial protocols, SOPs, regulations, and Good Clinical Practice standards. Your responsibilities will include maintaining the highest quality standards for trial monitoring activities, overseeing site activities to ensure protocol compliance, preparing detailed reports, updating CTMS systems, and providing support to the project team. You will also collaborate with stakeholders to track study progress, supervise data collection, and identify and address logistical challenges effectively. To excel in this role, you must have at least five years of clinical monitoring experience, a relevant life science degree or equivalent background, and a strong grasp of Good Clinical Practices and SOPs. Excellent communication skills, both written and verbal, proficiency in computer applications, and the ability to travel on-site as needed are essential. Your understanding of clinical trials, drug development processes, and medical terminology will be key to your success. At Allucent, we offer a comprehensive benefits package, competitive salaries, professional development opportunities, flexible working hours, and a supportive work environment that values growth and career progression. Join us to be part of a team dedicated to making a difference in the field of medical research. Please note that office-based employees are required to work in-office a minimum of two days per work week, with exceptions based on specific roles and locations. We do not accept unsolicited resumes from third-party recruiters and appreciate direct applications from interested candidates.,