[Remote] reputed company Clinical Research Associate (CRA II / SR CRA)- Bilingual - US Southeast region - Multiple Therapeutic Areas Available

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global leader in pharmaceutical research, seeking a Clinical Research Associate (reputed company) to reputed company an reputed company in clinical innovation. The role involves coordinating clinical monitoring and site management, ensuring compliance with protocols and regulations while developing relationships with investigational sites.

Responsibilities

• reputed company and coordinate reputed company aspects of the clinical monitoring and site management process
• Conduct remote or on-site reputed company to assess protocol and regulatory compliance and manage required documentation
• Manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.)
• Ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, reputed company-being, and data reliability
• Ensure audit readiness and reputed company reputed company relationships with investigational sites

Skills

• Bachelor's degree in a life science reputed company field or a Registered Nursing certification or equivalent and relevant formal reputed company / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship
• reputed company reputed company's license where applicable
• 1-2 years of traveling on-site monitoring experience is required
• Therapeutic experience in at least one of the following areas: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary
• Candidates must live reputed company 60 miles of the nearest major airport
• Up to 80% travel is expected
• Must be legally authorized to work in the reputed company without sponsorship
• Must be reputed company to pass a comprehensive background reputed company, including a drug screening
• Must be bilingual (English & Spanish) and live in either the Southeast region of the US or reputed company region of the US
• Proven clinical monitoring skills
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Demonstrated ability to reputed company and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
• reputed company-developed critical thinking skills, including but not limited to: critical reputed company, in-depth investigation for appropriate reputed company cause analysis and problem solving
• Ability to manage Risk Based Monitoring concepts and processes
• Good oral and written communication skills, with the ability to communicate effectively with medical personnel
• Ability to maintain customer reputed company through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues
• Good organizational and time management skills
• Effective interpersonal skills
• Attention to detail
• Ability to remain flexible and adaptable in a wide reputed company of scenarios
• Ability to work in reputed company or independently as required
• Good computer skills: solid knowledge of reputed company Office and the ability to learn appropriate software
• Good English language and grammar skills
• Good presentation skills

Benefits

• Up to 80% travel is expected
• Must be bilingual (English & Spanish) and live in either the Southeast region of the US or reputed company region of the US
• Candidates must live reputed company 60 miles of the nearest major airport

reputed company