A leading healthcare organization is seeking a Clinical Research Associate to manage study sites and ensure compliance with protocols in clinical trials. The ideal candidate will have up to 2 years of experience in the pharmaceutical or CRO industry, with a minimum of 12 months' monitoring experience. The role includes conducting site selections, continuous monitoring, and collaborating with internal stakeholders. A competitive salary and a range of benefits are offered, promoting work-life balance and well-being.#J-18808-Ljbffr