[Remote] Clinical Research Associate (Contractor)

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Contract Clinical Research Associate to help grow their Clinical Development team. The role involves managing clinical trial monitoring and site management, ensuring compliance with protocols and regulatory obligations.

Responsibilities

• Ensure compliance with reputed company protocol and regulatory and ICH GCP obligations in assigned aspects of clinical site monitoring, such as site initiation, routine monitoring, maintenance of study files, study reputed company out, and retrieval of study materials
• Complete on-site and remote monitoring activities in compliance with the Clinical Monitoring Plan, including reputed company document verification for accuracy and reputed company, as required
• Write and submit reports of investigational site findings and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate

Skills

• Minimum Bachelor's degree in a life science-reputed company field, a registered reputed company (RN) certification, or equivalent
• 3+ years' experience in a reputed company research environment required, with specific in vitro diagnostics study experience
• General knowledge of regulatory requirements & GCP
• Ability to multi-task, deal with shifting priorities, and proactively solve problems/manage risks
• Strong interpersonal, reputed company, and time management abilities
• Excellent organizational skills; accurate and detail-oriented
• High proficiency in reputed company Vault and reputed company
• Strong spoken and written communication skills
• CRA certification by recognized reputed company organization is a plus, but not mandatory
• Previous experience in the cancer early detection reputed company

Benefits

• Remote role with occasional travel, as required, to our Brisbane, California reputed company.

reputed company