Clinical Research Coordinator
Rivkin Westside Aesthetics, Brentwood, CA, United States
Rivkin Westside Aesthetics is a premier provider of cosmetic surgery and non-surgical rhinoplasty services in Los Angeles and Beverly Hills, California. Recognized globally for its innovative approach, the clinic is dedicated to delivering exceptional aesthetic results. Its offerings emphasize non-invasive procedures tailored to meet the unique needs of each patient. Located in the heart of Los Angeles, Rivkin Westside Aesthetics is a trusted name in transformative and patient-centric care.
Role Description
This is a full-time, on-site Clinical Research Coordinator role based in Brentwood, CA. The Clinical Research Coordinator will oversee clinical trials by ensuring adherence to protocols, regulatory guidelines, and study-specific requirements. Responsibilities include obtaining informed consent, coordinating research activities with study participants, monitoring clinical trial progress, maintaining detailed records, and collaborating with clinical staff to ensure timely and accurate data collection. The role will also involve facilitating communication between sponsors, investigators, and study teams for efficient research operations.
Qualifications
Experience in conducting Clinical Research and Clinical Trials
Proficiency in managing Protocols and ensuring compliance with study requirements
Familiarity with Informed Consent processes and ethical research guidelines
Strong organizational, time management, and communication skills
Ability to work independently in an on-site medical environment
Attention to detail and ability to maintain accurate documentation
Bachelor's degree in a related field, such as Life Sciences, Healthcare, or Nursing, preferred
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Role Description
This is a full-time, on-site Clinical Research Coordinator role based in Brentwood, CA. The Clinical Research Coordinator will oversee clinical trials by ensuring adherence to protocols, regulatory guidelines, and study-specific requirements. Responsibilities include obtaining informed consent, coordinating research activities with study participants, monitoring clinical trial progress, maintaining detailed records, and collaborating with clinical staff to ensure timely and accurate data collection. The role will also involve facilitating communication between sponsors, investigators, and study teams for efficient research operations.
Qualifications
Experience in conducting Clinical Research and Clinical Trials
Proficiency in managing Protocols and ensuring compliance with study requirements
Familiarity with Informed Consent processes and ethical research guidelines
Strong organizational, time management, and communication skills
Ability to work independently in an on-site medical environment
Attention to detail and ability to maintain accurate documentation
Bachelor's degree in a related field, such as Life Sciences, Healthcare, or Nursing, preferred
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