Clinical Research Associate II / Sr. CRA - Neurology/Parkinsons

New
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Rho IncCRO, Pharmaceutical, Biotechnology
Within a 1-hour commute of a US metropolitan airportFull-TimeSenior
Salary90000 - 140000 USD per year
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Job Details

Experience
4-5 years+
Required Skills
MS Office

Requirements

  • BA/BS, preferably in a life science, nursing, pharmacy or related field
  • 4-5 years+ of on-site monitoring experience within the CRO, pharmaceutical, or biotechnology industry
  • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
  • Computer literacy, including proficiency in MS Office
  • Proficiency in use of EDC systems
  • Strong written, verbal and presentation skills
  • Attention to detail and understanding of high-quality scientific standards
  • Strong organization skills
  • Honesty and integrity
  • Willingness to learn and train
  • Critical thinking abilities
  • Agile and adaptable
  • Proven monitoring skills

Responsibilities

  • Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)
  • Participate in the site selection process with oversight from the Clinical Team Lead role
  • Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved
  • Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials
  • Provide mentoring, training, and co-monitoring of junior clinical team members
  • Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements
  • Attend and present at meetings and conferences, including Investigator Meetings
  • Participate in the RFP process, including business development meetings
  • Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials
  • Perform both onsite & remote monitoring and study closure activities across multiple protocols
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90000 - 140000 USD per year
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